Abstract
Cancer is the second cause of death after cardiovascular diseases. With due attention to rapid progress in the phytochemical study of plants, they are becoming popular because of their anticancer effects. The aim of this study was to investigate the effective medicinal plants in the treatment of cancer and study their mechanism of action. In order to gather information the keywords “traditional medicine,” “plant compounds,” “medicinal plant,” “medicinal herb,” “toxicity,” “anticancer effect,” “cell line,” and “treatment” were searched in international databases such as ScienceDirect, PubMed, and Scopus and national databases such as Magiran, Sid, and Iranmedex, and a total of 228 articles were collected. In this phase, 49 nonrelevant articles were excluded. Enhancement P53 protein expression, reducing the expression of proteins P27, P21, NFκB expression and induction of apoptosis, inhibition of the PI3K/Akt pathway, and reduction of the level of acid phosphatase and lipid peroxidation are the most effective mechanisms of herbal plants that can inhibit cell cycle and proliferation. Common treatments such as radiotherapy and chemotherapy can cause some complications. According to results of this study, herbal extracts have antioxidant compounds that can induce apoptosis and inhibit cell proliferation by the investigated mechanisms.
Keywords: toxicity, medicinal herbs, plant compounds, cell line
Cancer is one of the major causes of death in the world, and it is the second leading cause of mortality after cardiovascular diseases.1 Cancer starts with the deformation of a natural cell caused by genetic mutations in DNA. This abnormal cell reproduces in an abnormal way by asexual reproduction, that is, it ignores signals related to regulation of cell’s growth around it and obtains invasion characteristics and causes changes in surrounded tissues.2
Cancer is an important health problem in developing and developed countries. Every year, an average 182 per 100 000 persons suffer from cancer worldwide, and 102 die by cancer. According to the World Health Organization, 14 million people suffer from cancer and 8 million die by cancer worldwide. The prevalence rate of cancer in Iran is 7/134 per 100 000 people. Based on this statistics, 85 000 people suffer from cancer in Iran each year, and 55 000 people die from cancer.3 Mortality caused by cancers is increasing throughout the world, and it is predicted that more than 13.1 million deaths will occur due to cancer worldwide by 2030.4
Nowadays, various methods are used for cancer treatment such as chemotherapy, but in this method, because of nonselectivity of medicines, a high percentage of healthy cells will be lost with cancer cells. The most important problem in cancer treatment is destroying tumor cells in the presence of natural cells, without damaging natural cells. In order to prepare anticancer medicines from natural resources like plants, testing cytotoxic compounds and screening raw extracts of plants is necessary.5
Therefore, availability of natural products with higher effectiveness and lower side effects is desired.6 Medicinal herbs are important for cancer treatment due to their multiple chemical compound for discovering new active materials against cancer.7
Plants produce a wide range of chemical compounds that apparently have no direct role in the plants’ growth. These compounds are called secondary metabolite. Alkaloids, terpenoids, flavonoids, pigments, and tannins are important constituents of these compounds. Secondary metabolites have biologic effects such as anti-inflammatory, anticancer, contraceptive, and different effects on hematopoietic cells,8 lipids,9 and cardiovascular systems.10
Different improvements are reported in common treatments of cancer by finding secondary compounds of natural products and medicinal herbs. It is believed that anticancer effects of plants develop by suppressing cancer’s stimulating enzymes, repairing DNA, stimulating production of antitumor enzymes in cell, increasing body immunity, and inducing antioxidant effects.11
Cancer is a painful disease and fighting against this disease is very important for public health. Regarding the fast progress in the phytochemical study of herbal products, plants are transforming to popular anticancer sources. In cancer, initial tumors will be treated by chemical supplement therapies or surgery. But cancers in the metastasis stage will resist against care.12
But in chemotherapy, due to nonselectivity of used medicines, a high percentage of healthy cells will be destroyed with cancer cells. Nowadays, more than 60% of anticancer compounds that are useful for cancer patients are obtained from herbal, marine, and microorganism sources.
The positive effect of plants in cancer treatment have been studied extensively and has shown positive results.13 Also, different researches and studies have proved the positive effect of plants in curing diabetes,14 fertility15 and sterility,16,17 thyroid disorders,18 anemia,19 and psychological disorder.20 Finding plants that replace chemotherapy and cumbersome cures of cancer with cytotoxic effects is necessary.21
In previous article,13 we tried to systematically study some effective Iranian plants in cancer treatment. In this article, we want to study plants, their important compounds, and effective mechanisms in detail.
Methodology
In order to collect data about different compounds, keywords “traditional medicine,” “plant compounds,” “medicinal plant,” “medicinal herb,” “toxicity,” “anticancer effect,” “ cell line,” and “treatment” were searched in domestic databases such as Magiran, Sid, and Iranmedex and international databases like ScienceDirect, PubMed, and Scopus. Searches were limited to articles in English and Persian languages, and the search interval was from 1975 to 2016. A total of 228 articles were collected. Among these, 49 articles were excluded because they were irrelevant. Finally, information was obtained from 179 articles and entered in this survey.
Findings
Achillea wilhelmsii
Achillea plant with scientific name Achillea wilhelmsii is from Asteraceae order and Compositaea genus. Achillea has different species but Achillea wilhelmsii is more frequent in Iran and grows in different areas. Achillea wilhelmsii is a gramineous, perennial, and short plant of 15 to 40 cm.
Methanol extracts and essence of leaves of this plant have cytotoxic effects on colon cancer cells (HT-29) and cytotoxic effects of essence are higher.22 In other studies, effects of methanol extracts of plant’s leaves against cell lineage of colon cancer and cancer of stomach and breast are shown.23 Methanol extract of plant contains phenol compounds, especially flavonoids, which suppress reproduction of cancer cells through inducing apoptosis.24,25 One of the most important monoterpene compounds of this plant that causes apoptosis in human melanoma cells is 1,8-cineole and α-piene in plants’ leaf essence.26
Allium sativum L
Allium sativum is a plant from Aparagales order, Amaryllidaceae family, Allianceae subfamily and Allium genus. Allium sativum is a garmineous and permanent plant, with a stem size of 40 cm. Its underground part is inflated and composed of 5 to 12 parts enclosed in fine and slender membranes in gray-white. Its leaf is thin and filet in dark green, and its flowers are small and pink like an umbrella at end of the stem.
Various research have shown that Allium sativum and organosulfuric compounds reduce the risk of cancer in breast, larynx, colon, skin, womb, gullet, bladder, and lung.27,28 In other research, we refer to the role of the most important Allium sativum compound, that is, Allicin, and the antitumor characteristics of this compound on breast and prostate cancer are proved. This compound induces planned death of cells and has a anticancer role.29,30 When Allium sativum is crushed and cracked up, Allicin 1, under the effect of an enzyme, changes to Allicin 2. Allicin is a proliferation inhibitor of malignant human cells. Ajoene is another compound that suppresses proliferation of leukemia and will cause planned death of cell.31,32
Ammi majus
A white flower with scientific name Ammi majus belongs to Apiaceae family, and it is an annual and dicotyledonous plant with autumn germination. It is a long and thin plant that grows to 100 cm in general conditions, in wet and soft lands, saline grassland, and coastal areas. This plant is cultivated in Europe and Mediterranean area, western Asia, and even in India.33
The effect of ethanol’s extract of this plant on HeLa and MCF7 was studied and results showed that this plant’s extract has toxic effect on these cells.34 Comorian compounds (as part of phenol compounds) are major compounds of this plant, and main biological activities of this plant are attributed to them. Research has referred to cell toxicity of coumarin compounds on cell lineages, and apoptosis induction by these compounds is studied and confirmed. Psoralens are the most important coumarin compounds of this plant that can play an anticancer role, inhibiting cytochrome p450 activity.35
Ammi visnaga
Ammi visnaga L is a garmineous and perennial plant that grows in Mediterranean areas. This species is divided into 3 components: alegrian, furanochromones, and flavonoids.36 It is seen in the north of Iran in Geilan, Roudbar, Manjil and in south of Iran in Bushehr and Shahbazan at a height of 800 meters. Its leaves have more cuttings and its flowers are white and umbellate. This odorant plant is of Apiaceae family, and its antibacterial, antifungal, and therapeutic effects in vitiligo have been published.36,37
The killing activity of different extracts of the above-ground part of this plant on T47D cancer cells has been studied.38 Also, the inhibitory and dose-dependent effect of this plant on 2 human cell lineages, pelvic rhabdomyosarcoma and L20B of mice, have been proven.39 Khellol, visnadine, cimitugin, and β-sitosterol are the most important compounds of this plant. Flavonoids like quercetin and kaempferol are isolated from the aqueous extract of this plant, and these compounds can justify the anticancer effects of this plant.40
Artemisia absinthium L
Artemisia is a plant in the Asteraceae family. Artemisia has 200 to 400 species that have clustered and bitter flowers. One species, Artemisia absinthium L, is native of Asian moderate areas, north of Africa, and vast areas of America. The size of this plant is 80 to 120 cm. Flowers of this plant are yellow and clustered.41
A research on breast cancer cells MCF-7 has been reported.42 Similar results related to the anticancer characteristics of this plant on 3 cancer cells HeLa, HT-29, and MCF7 have been reported. In a study about the Artemisinin effect of this plant on breast cancer cells, it was determined that plethoric reaction in cancer cells involves inhibiting cell’s growth, apoptosis, preventing angiogenesis, preventing cell migration, and decreasing responses of core receptors.43 Quercetin, isorhamnetin, kamfrolinalol, alphapinin, limonene, and myrecene are the other compounds of this plant.
Quercetin inhibits growth of many cancer cells such as MCF-7, and isorhamnetin inhibits growth of many cancer cells such as MB-435, SKMEL-5, Du-145, MCF-7, and DLD.44 Also, artesunate is one of the most important artemisinin that has angiogenic effect, and in addition to anticancer effects on K569 (leukemia cancer), it inhibits the production of angiogenic factor VEGF.45 In other research, alpha-pinene, beta-pinene, limonene, and myercin available in the plant are probable factors of inhibiting the growth of human breast cancer and hepatic and melanoma. Alpha-pinene, beta pinene, and limonene available in methanol and ethanol extracts of this plant are inhibitory factor of HT-29 cells (colon cancer).46
Astragalus cytosus
Astragalus cytosus is perennial plant from the Leguminoseae family and its height reaches to 75 cm. Its reproduction is done by seeds. Its stems are dark purple. Its leaves are composed of leaflets that are placed in 11 to 30 pairs in each leaf’s axis. Its flowers are usually amethystine, blue, or white close to the end of flowering branches.
More than 200 species of Astragalus cytosus grow in Iran. In a research on HeLa cancer cells, the effect of toxicity of this plant’s extract on cancer cell was shown.47 Also in a clinical study on 24 patients suffering from lung cancer, 21 patients showed positive response to this plant’s extract.48 In vitro studies show that flavonoids in other species of this plant can direct carcinoma cells to apoptosis.49
Astrodaucus orientalis
This is biennial plant from the umbellate family. Extract of root and above-ground part of this plant show antiproliferation effects on breast cancer cells (T47D).50 α-Pinene, α-thujene, α-copaene, fenchyl-acetate, anisole, myrecene, and sabinene are the most important compounds in this plant.51,52 Inhibition of cell cycle and also induction of apoptosis is the main mechanism of anticancer effects of the plant.50
Avicennia marina
Avicennia marina is species of mangrove plants. Mangrove plants are halophyte plants resistant against sea salt. Mangrove is dominant species in the Mangro ecosystem. This plant is like a bush or shrub with a height of 1 to 10 meters. It has a white shell or gray or yellowish green, and its leaves are oval or sharp. Its flowers have 4 white or yellowish orange petals.
Flavonoid compounds of its leaf extract have anticancer effect on human breast cancer BT-20 cells. In another study, by separating naphthoquinone from leaf of the plant, anticancer effect of this compound on laryngeal cancer cells (kb) was shown.53 A cytotoxic effect of the extract on breast cancer cells (row 231MDA-MB) is confirmed.54
Boswellia serrata
Boswellia serrata is a medical plant from Spindales order and Burseraceae family with names Olibanum or Frankincense. It is obtained from specie B sacara, B frereana, and B serrate in Bosoolia. Hydroalcoholic extract of this plant causes death of cervical cancer cells (HeLa cell) and this effect is dependent on dosage and time.55,56
In another study, alcoholic extract of frankincense resin caused disorder in the biosynthesis of DNA and RNA and proteins inhibit the tumor growth and induce apoptosis in cancerous cells in mice. In a research on leukemic cells HL60, it was shown that frankincense reduces viability of the cells.57,58 Monoterpene, diterpene, and triterpene and boswellic acid are the main ingredients of frankincense resin, which can induce apoptosis in cancerous cells.59 In fact, frankincense extract, by increasing production of reactive oxygen species and by activating caspases, causes apoptosis and severe damage to cells.60
Camellia sinensis
This plant is a kind of tea that is obtained from the buds and petals of fresh herb. In the process of producing this tea, little oxidation occurs. Tea is a natural source of caffeine, theophylline, thianin, and antioxidants. In a study on rats, it was found that green tea could inhibit 5-alfardoctase enzymes. This enzyme converts testosterone to di-hydrotestosterone, which is a prostate carcinogenic agent. Accordingly, it has been found that green tea can have an inhibitory effect on prostate cancer.61
In this regard, the antitumor effect of green tea on prostate cancer has been shown.62 Green tea contains polyphenols such as epicatechin, epigallocatechin, epigallocatechin, and epigallocatechin-3, which have anticancer effects.63–65 Cytotoxic effects of green tea on breast cancer cells has been demonstrated.66
In a research conducted by Wang and colleagues in China, they concluded that green tea drinking habits, including regular drinking, greater amount of intake, and lower temperature were associated with reduced risk of gastric cancer.67
Citrullus colocynthis
Citrullus colocynthis belongs to Cucurbitales order and Citrullus genus. Used part of the plant is yellow and a very bitter fruit with the size of an apple.68 A study showed that the extract of this plant may (Hep2) have toxic effects on larynx cancer cells.69 According to studies, chemical constituents of this plant such as cucurbitales are used as anticancer medicine in cancers such as liver (HepG2) and breast (MCF7) cancers; quercetin and β-sitosterol as antitumor agents have been studied in in many researchs. These compounds act by inhibiting cell cycle (cycle stops at G2/M), and the induction of apoptosis can impose anticancer effects.70–73
Saffron (Crocus sativus L)
Saffron Crocus sativus L belongs to the Iridaceae family. This plant in Iran is native of Khorasan. Saffron is a perennial plant, with height 10 to 30 cm, from the bulbs of this plant, with narrow leaves exits. This plant has 1 to 3 purple flowers. The used part of this plant is stigma, known as saffron.74
Various studies showed anticancer effect of the saffron extract on cancer cells in vitro; for example, Escribano et al, in a study on the effect of saffron extract on human cancer cells, found that the materials separated from saffron such as crocin, crocetin, picrocrocin, and safranal induced apoptosis in cancer cells.75,76
In another study, the effect of saffron extract and other major plant substance called quercetin on colorectal cancer cells was studied and the results showed the toxic effects of this plant on these cells.77 Another study also showed the anti-angiogenic effects of this plant on breast cancer cells (MCF-7), and extract of this plant inhibits angiogenesis in these cells.78
In fact, the saffron extract, by inhibiting DNA synthesis, can exert its anticancer effects.79 However, in the consumption of high doses of this herb, the necessary precautions should be taken because according to Rahimifard et al’s study on the human cervical cancer cells, larynges cancer cells, and natural human monkey kidney, it was observed that toxicity on natural cell is higher than 2 cancer lines, which indicated precaution in consumption of high dose of saffron.80
Another research has studied effect of cellular toxicity and apoptogenic properties of saffron extract on the cancer cells and concluded that saffron can play an important role in cell death of HeLa and HepG2 cells and apoptosis. Saffron can be used as a chemotherapeutic agent to treat cancer in the human in future.81
Curcuma longa
Turmeric is a plant with scientific name Curcuma longa from the Zingiberaceae family. This perennial plant usually requires humid and rainy environment. The main habitat of turmeric is hot areas of Asia such as India, Pakistan, Indonesia, and southern China, and it is native of Africa and South America. Turmeric has underground stem called rhizome. Several aerial shoots as high as 1 to 1.5 meters exit from these rhizomes. Edible part of turmeric is dried rhizomes.82
The study of cytotoxic properties of turmeric on liver cancer cells (Hep-2) showed that the cytotoxicity mediated by curcumin in a dose-dependent manner leads to apoptosis of cancer cells through mitochondrial pathway.83
The results of studying the effects of its extract on telomerase activity in breast cancer showed anti-proliferative and inhibitory effects of telomerase.84
In another study, it was found that turmeric imposes its cytotoxic effects on lung cancer cells through inhibition of telomerase activity in a dose-dependent manner.85
Curcumin, as an important ingredient of turmeric, plays a significant role in the prevention and treatment of primary ovarian cancer, and multiple clinical studies have proven its effectiveness.86
The anticancer potential of curcumin against cancers, including leukemia, lymphoma, digestive, urinary, reproductive, breast, uterus, ovary, lung, melanoma, colon cancers, and brain tumors have been shown.87 Free radicals and toxic products of oxidative stress play a significant role in the development of many diseases, including cancer, and curcumin has antioxidant effects that reduce or inhibit damage caused by free radicals.88
One study showed that treatment of human blood lymphocytes with curcumin significantly reduces genetic damage caused by radioactive iodine-131.89 Another study showed that curcumin induces apoptosis and inhibits proliferation of cancer cells. Apoptosis occurs due to release of cytochrome and its effect on P53 protein as well as the effect on intracellular signals is responsible for stopping cell growth.90 In fact, the mechanisms by which curcumin inhibits tumor formation are combination of properties including antioxidant, anti-inflammatory, anti-angiogenic, anti-metastatic, inhibition of cell cycle, and proapoptotic, which induce inhibitory effects on the cancer through regulating genes and molecules involved in these paths.91
Ferula assa-foetida
Ferula assa-foetida plant grows in Iran in different regions of Khorasan, Sistan, and Baluchestan and southern parts of Iran such as Kerman, Dasht-e Murghab, Abade, and Nain. Asafoetida is a perennial plant with strong, thick, and fiber stems. Used part of this plant is a resin, which is used as a gum.
Cytotoxic effect of ethanol extract of asafoetida on liver cancer cells has been proved (category HepG2).92 Also, consuming gum of this plant has significantly reduced the risk of colon cancer.93 The most important ingredients in coumarin compounds are sulfur-containing compounds, and compounds such as β-sitosterol and oleic acid. In order to justify anticancer effects of ethanol extract of this plant and orgnosulfuric compounds, different mechanisms are suggested, including inhibition of gene mutation, effect on the activity of enzymes, inhibition of DNA destruction, effect on cell proliferation, and changing the activity of enzyme.94,95 However, induction of planned cellular death is an important mechanism for anticancer effects of this plant.96 Cytotoxic activity of phytochemical compounds in some species of Ferula against cell lines including ovarian carcinoma (CH1), lung cancer (A549), and melanoma (SK-MEL-28) has been studied, and it has been shown that these compounds can have mild killing effect on cells.97
Glycyrrhiza glabra
Glycyrrhiza glabra is wild plant from vegetables family, native to southern Europe, North Africa, and temperate regions of Asia. It grows in most parts of Iran, especially in the eastern and northeastern Khatam Marvast city and territories as well as Azerbaijan and Eghlid city. Its leaves are compound and consists of 4 to 7 leaf pairs plus an end leaflet that is sticky due to secretion of juice. Flowers are blue and its fruit contains 5 to 6 brown seeds. Its roots and stems have medical use.98 Extract contents of the root lead to morphological changes in the mammary cell line 4T1 and reduce their viability.99 Its root extract induces BCL2 phosphorylation and, like Taxol, inhibits the cell cycle at the G2/M phases in tumor cell lines.100
Glycyrrhizin, is a triterpene glycoside that is the main compound in root extract and acts as an anti-proliferative agent against tumor cells, especially breast cancer cell line (MCF-7) and HEP-2 and plays its role by inducing apoptosis.101,102
Glycyrrhiza glabra root extract induces apoptosis in HT-29 cells; therefore, it is useful in the treatment of colon cancer.103
Lagenaria siceraria Standl
Bottle gourd is a species of Cucurbits that has yellow skin and is less edible. This plant has a very large head and a small head and a narrow waist. The naming of the pumpkin is because of its shape. The effect of the plant extract on human lung cancer cell line A549 has reviews, and it has been shown that the extract could significantly inhibit the cell line.104
Antitumor effect of methanol extract of aerial parts of this plant has been demonstrated.105 In another study, water-soluble polysaccharide isolated from this plant and its effect on carcinoma of human breast cell lines (MCF7) has been proven.106 In addition, its fruit is a source of vitamin C, beta-carotene, vitamin group B, saponins, and cucurbitacin. Cucurbitacin belongs to 4-ring terpenoids that has cytotoxic activity.107,108
Lepidium sativum
Watercress is an annual plant that is known as Jrjizbastany and Rashad in Iranian ancient medicine. It has light green leaves, small red or white flowers with gentle fragrance that jointly appear at the end of branch. The fruit is oval with an approximate length of 50 mm and a width of 4 mm. Cytotoxic effects of methanol extract of cress seeds on the bladder cell line (ECV-304) has been reported.109 Also, Aslani et al have shown, in a study of aerial parts of the plant, the cytotoxic effect on K562 leukemia blood lines.110 In another study, the effects of aqueous extract of seed on breast cancer cells (MCF-7) through induction of apoptosis have been demonstrated.111
This plant is rich in antioxidants such as vitamins E, C, B, A, isotiosinat, and omega-3 fatty acids such as alpha-linolenic acid as well as glucosinolates, and these compounds can impose their anticancer effects through antioxidant properties and inhibit the proliferation of plant cell.110,112
Medicago sativa L
Alfalfa is plant with scientific name Medicago sativa L that is usually found in most parts of the world and has been used in traditional medicine for the treatment of various diseases such as hepatic disorders.113 Phytoestrogens in the plant and strong estrogenic activity of this plant is useful in treating hormone-dependent cancers.
Alfalfa contains large amounts of almost all vitamins, flavonoids, digestive enzymes, coumarin, the alkaloid amino acid, and trepans, and it is also useful for breast cancer and also increases the breast milk. Alfalfa contains triconlin, which is a plant alkaloid compound and has a hormone role in the plant. It is believed that this plant alkaloid has important medicinal properties such as anticancer effects.114,115
Mentha pulegium
This plant with the scientific name Mentha pulegium and the English name European pennyroyal belongs to the Labiaceae family. Pennyroyal is a gramineous plant, and its shrubs grow to a height of 60 cm, and grows wild in many fields. This plant has oval leaves and small, regular sharp teeth. Flowers of this plant with leaves and stalks are mostly in the upper shaft and the colors are purple.
Aslani and colleagues reported research before flowering the plant’s cytotoxicity effect on leukemia cells. There are natural substances that are included in Pennyroyal polygon, mentone, piperitone, limonene, isomenthone, and Octaan-3-ol;116 in some studies the inhibitory effect of flavonoids on proliferation of cancer cells via apoptosis induction refers to Pennyroyal.117
Myrtus communis
The scientific name Myrtus or Mort is a genus of Murdian. Genus of evergreen shrubs or trees with 1 or 2 species native to southern Europe and North Africa are Murdian. This plant is an evergreen shrub or bush that sometimes reaches a height of 5 meters. Its leaves are about 3 to 5 inches long and have a nice smell. It has petals of white color and blue ball-shaped fruits.118 In some studies, the plant has been referred for its anticancer effects. The plant also shows cytotoxic activity on cancer cell lines MCF7.119–121 Polyphenols, myrtucommulone, semi-myrtucommulone, 1,8-cineole, α-pinene, myrtenyl acetate, limonene, linalool, and α-terpinolene are some of the most important compounds found in this plant.118 In most studies anticancer properties of this plant are attributed to plant phenolic compounds (especially mitocomolon). Cell cytotoxic effects are on their cell layer.122
Induction of apoptosis in cancer cells due to external and internal ways is a mechanism to deal with cancer cells.123
Nigella sativa
Black seed is of the Ranunculales Ranunculaceae family. This annual flowering plant is native to southwest Asia. This plant grows in abundance in Arak and Isfahan in Iran. A study presented an overview of the antioxidant protective effects on the liver of the anticancer effects of the plant Nigella.10 In this context, evaluation of alcohol on the effects of Nigella sativa on kidney cancer cells (ACHN) showed an apoptotic effect on these cells.124 Its Kvyynvny compounds and dinitro-quinone are like thimoquinone.125 In a study of colorectal cancer cells, the effects of thimoquinone on inhibiting cancer cell growth, apoptosis, and increased cell morphological changes was shown. It also has been shown to induce programmed cell death, with the anticancer activity being observed in an alcoholic extract of Nigella sativa.126–129
In a study the effect and mechanism of black beans has been shown in the treatment of breast cancer.130
In a research conducted by Elkady and colleagues, the effect of Nigella and the mechanism in the treatment of colon cancer in humans was demonstrated.131
Olea europae
Olive plant with the scientific name Olea europae L contains approximately 35 to 40 species and belongs to the family Oleaceae. Since ancient time hot or lukewarm areas such as the Mediterranean, North Africa, Southeast Asia, north to southern China, Scotland and East Australia have a wide distribution. Olive tree leaves are narrow, dark green, and permanent evergreen. Olive flower clusters have leaves that appear from the side and have 4 petals and 2 flags and flower cluster.132
In a study of the anticancer effects of olive oil, the most important leaf and its compounds (especially oleic acid) are mentioned.24 In other anticancer effects, pinoresinol found in olive oil has an effect on colon cancer.133 The role of phenolic compound oleuropein in olive oil is also important, suggesting that this compound acts directly on the her-2 gene in breast cancer cells and controls.134 The study also showed that acidic triterpenes found in olive oil can inhibit tumor cell proliferation and induction of apoptosis in some categories. Two of these compounds, maslinic acid and oleanolic acid, showed acceptable antitumor effect on colon cancer model in rats, and these compounds inhibiting tumor growth and angiogenesis are important factors.135
Pegaum harmala L
This herbaceous perennial plant is from the perennial family Zyqophyllaceae Nitrariaceae. This plant grows in Mediterranean regions such as North Africa, Turkey, Syria, and usually grows in arid lands. It grows to about 30 to 50 cm length, and has a plant-like appearance, with green leaves and regular water-filled narrow divisions. It has large flowers with greenish-white sepal and large petals. Its extract also reduced the viability of epithelial cervical carcinoma cells and carcinoma of the colon.136 This plant is made up of mainly alkaloids and these alkaloids have anticancer effects. In another study that was conducted using chemical analysis, the antioxidant activities of these alkaloids against human breast cancer cells were noted.137
Physalis alkekengi
It is a perennial herbaceous plant with creeping rhizome stems of potato corners. The effect of aqueous extract of this plant on U937 cell cytotoxicity was positive.138 The basic compounds of physalin plants belong to the group of triterpenoids. Anticancer cytotoxic activity of physalins B and M extracted from the plant on cancer cells (especially human cell line HeLa and Hepatum cell lines SMMC-7721 and HL-60) is verified.139
Polygonum aviculare
Caryophyllales Polygonaceae plant belongs to the genus Polygonum. Aviculare plants grow throughout the year and the chronometer stem reaches a length of 50 centimeters. Its leaves are small and sharp, with tiny pink flowers in it. This plant grows in most areas of Asia, Europe, Africa, and America and in most parts of Iran. In some studies, the effect of the extract on the inhibition of proliferation of cancer cells HeLa has been reasonable.140,141 The effects on cell proliferation and expression of apoptotic genes in breast cancer cells (MCF7) showed that extracts of the plant through the induction of apoptosis can cause cytotoxicity in cancer cells of breast.142 Tannins, flavonoids, and alkaloids are the most important components of this plant.143 However, studies of anticancer effects showed that despite phenol compounds the effects of the plant is considered the main cause.140,142
Rosa damascenes Mill
Rose or rose (scientific name: Rosa damascenes Mill) has long been cultivated in different climatic conditions. It is from the family Rosaceace and the flowers and leaves of the plant are its active ingredient is tannin. It is a perennial shrub, close to 5.1 meters in height, and has a cylindrical shaper without grooves.
The toxic effects of this essential oil on lung cancer cell lines (A549) and breast (MCF7) have been reported. The ethanol extract of the plant cell has killing effect on cervical cancer cells (HeLa).144 Rosa Damascena essential oil affects gastric cancer cells in 2 specific ways: the soluble phase increases cell viability, while the vapor phase decreases cell survival. Also, flow cytometry showed that apoptosis is the important mechanism accompanied with cell death.145
Silybum marianum
It belongs to the family Astir Asteraceae. Milk thistle is a plant native to the Mediterranean and spread throughout Europe. It grows in vegetative arid land, roadsides, arable land, and similar places such as beaches and mountains. The vehicle and shrubs are for the duration of 1 or 2 years. It appears from 30 to 200 cm and its cone-shaped flower colors are red to purple.146
Also a study has shown that silymarin causes cell cycle arrest and apoptosis on the 4T1 cell line.147
Taverniera spartea D
Silver spartea plant with the scientific name Taverniera spartea D usually grows on the southern coast of Iran including Bandar Abbas, Minab, and Baluchistan. This woody plant, shrubs growing to a height of 50 to 110 cm, is covered with fluff on a bed, with short shoot. The flowers of this plant are purple and pink. This plant is flowering to March.21 Methanol extract of the plant, especially chloroform fractions, showed toxic effects on breast cancer cell lines (MCF-7 and BT474) and human prostate cell lines (PC-3 and DU-145).21 The anti-cancer effects of the plant have been reported.
Taxus baccata L
Yew tree with the scientific name Taxus baccata L is gymnosperms from the family Taxaceae. There are 3 species of yew trees, and Taxus baccata L is the only species native to Iran. Yew is an evergreen tree with a very long life and slow growth. This tree has a smooth trunk has a height of up to 30 meters and diameter up to 5 meters. This species is native to Europe, the Caucasus, North Africa, and Iran. Yew in the woods of northern Iran is often Azadshahr from Astara. Yew tree grows at high altitudes in mountain areas, deep dark valleys, steep slope ranging from rocky and semihumid to wet and cold conditions.
This plant is one of the first plants on which extensive research has been done on the effects of cancer prevention. Taxol is one of the natural ingredients of the plant that has anticancer effects.148,149 A study has shown that the acetone-dichloromethane extracts of the plants have a cytotoxic effect on cancer cells k562, HeLa, and MDA-MB-468.150
Thymbra spicata
Zufaee thyme plant is from the family Labiaceae, and the plant grows preferably in dry and sunny areas and on the slopes of dunes. There are various plants that grow to 15 to 40 cm in height and has flowers that are purple. It is because of thymol and carvacrol that there is biological activity. Various parts of the plant essential oil is a good source of antibacterial and antioxidant properties. Hydro-alcoholic plant inhibitory effect on lung cancer cells (SK-Mes-1) has been shown.151 Thyme, thymol, and carvacrol are the most important plant phenol compounds with antioxidant properties, prevents oxidative damage to DNA, and thus can prevent cancer.152
Thymus vulgaris
Thymus vulgaris L has the the English name garden thyme. It belongs to the family Lamiaceae and has a straight stem and is herbaceous or woody and grows to a height of 20 to 30 cm. This plant has branched stems that are covered with white fluff. This plant has aromatic leaves that are usually evergreen and flowers are pale purple to white in color.
In the prostate study on rats it was found that thyme extract inhibits the growth of abnormal and precancerous lesions and treats153 and also inhibits the growth (in laboratory conditions) of squamous cell carcinoma of the head and neck.154,155 This plant has a variety of compounds, including flavonoids. Thymol and carvacrol are the most important plant phenol compounds that are useful in the treatment of breast cancer and colorectal cancer.156
A study proved that thyme inhibits proliferation of human colorectal cancer cell migration and invasion.156
In another study, the effect of inhibiting growth was proved in human breast and colorectal cancer.157
Trigonella foenum-graecum L
Fenugreek or Shanblid (scientific name: Trigonella foenum-graecum) is a plant of the Fabaceae family with height of 10 to 50 cm with single flowers that are bright yellow to brown. This plant is native to Iran and in most parts of Iran, including Azerbaijan, Isfahan, Fars, Khorasan, Semnan, and Damghan and are edible vegetables.158 In a study of the effects of crude extract of fenugreek, there was selective cytotoxicity against some cell lines such as MCF7, TCP (T-cell lymphoma), FRO (thyroid papillary carcinoma), and brain tumors.159 It is also protective effect against breast cancer induced by DMBA (7,12-dimethylbenz(a) anthracene) in mice.160
In another study, the inhibitory effects of the plant extract on the growth of cancer cells EAC was shown. Flavonoids and alkaloids in the plant, such as ginger, cadence, zinger one, vanillin, and eugenol, have been shown to be involved in anticancer effects.159–162 The main mechanism of anticancer activity is apoptosis induction.159,160
Urtica dioica L
Nettle (scientific name: Urtica dioica) is a grassy, herbaceous perennial with branched legs. Shoot is straight and square, and leaves of bitter Azkrk are covered. It can be seen in the wile in Iran near Tehran, in Karaj in Alborz slopes, and the hive Shemiranat, and in the northern regions in Mazandaran and Gilan and Drazrbayjan, on the slopes of Sahand, Zanghab, and Lorestan (in the river).163 Studies have shown cell proliferation inhibitory effect on prostate cancer cells (LNCaP and as hPCPs) by aqueous and ethanol extracts of the plant.164–166 Also, a report has referred to the anticancer effects of this plant against esophageal cancer.167 Plant compounds with antioxidant phenol compounds are those that may have an important role to prevent cancer. In a study, the anti-proliferative effect on human prostate cancer cells by nettle root extract has been proven.168
Vinca rosea
Belonging to the genus Vinca and oleander it has for a very long time been an important medicinal plant of great concern. In a study on human skin cancer cell line A431, the methanol extract of the plant had a positive effect on reducing the proliferation in this category.169 Alkaloids such as vincristine, vindoline, vinblastin, vinflunine, and catharantin in the aerial parts are different from vincristine and vinblastine, and among them 2 combinations of plant secondary metabolism are used today as anticancer drug.170,171 The effects of this plant’s alkaloids on cancer cells of breast, prostate, cervix (MCF-7, PC3-1C, HeLa) were studied, indicating that these alkaloids’ tubular protein links changed its structure by blocking the division of cancerous cells; these compounds with antioxidant properties will prevent cancer cells from progression.169,172
Viola tricolor
Violet plant with the scientific name Viola tricolor. Violets are herbaceous plants, resistant to cold throughout the year and grows to a height of up to 25 cm. Small flowers of this plant with different colors including bright and family purple, white, and yellow flowers that appear in spring and summer and become the fruit capsule. Aqueous extract of this plant has a strong inhibitory effect on proliferation of cervical cancer, and the active ingredient of the plant responsible for this effect is ethyl acetate.173 This plant contains a number of compounds that have cytotoxic effects of potent cells.174 Studies have shown that flavonoids can have anticancer effects.175,176
Zingiber officinale
Zingiber officinale is a member of the Zingiberaceae family. Ginger or ginger or Shengir is an edible and medicinal plant. It is grown all over India, especially in hot and humid areas. Ordinary ginger rhizomes of ginger powder is spicy and aromatic spices are used for savory dishes traditionally.177 This plant has bright green slender stalks that grow from glandular stem. Ginger flowers are yellowish green with purple edges and pale spots.
The aqueous extract of Zingiber officinale is effective on breast cancer cells (MCF-7 line and MDA-MB-231), and morphological changes observed in cancer cells that were extracted under array indicate that cell death induction program has been destroyed.178,179
Conclusion
Several therapeutic procedures are available for the treatment of cancer, and in most cases, undesirable side effects (gastrointestinal disorders, kidney damage, and other complications) are associated with them. These compounds include alkaloids, phenol compounds, and monoterpenes. In addition to these, indicators such as vinblastine, vincristine, curcumin, Taxol, boswellic acid, and umbelliprenin and compounds such as quercetin, catechin, cucurbitacin, kaempferol, thymol, carvacrol, 1 and 1,8-cineole, α-pinene, myrecene, and β-sitosterol have anticancer effects. These compounds have antioxidant properties, and inhibition of damage to DNA, cell cycle arrest (especially at the G2/M), induction of apoptosis, inhibition of angiogenesis in tumor cells, and its anticancer effects are new and more effective.
Acknowledgments
This study was the result of a research project approved by code 1395.104 by the Research Deputy of Kurdistan University of Medical Sciences and was conducted under its financial support. We would like to appreciate those who paid special attention to this project.
Footnotes
Author Contributions: Study concept, design, and critical revision of the manuscript for important intellectual content: Wesam Kooti, Karo Servatyari. Drafting of the manuscript and advisor: Majid Asadi-Samani, Masoud Behzadifar, Fatemeh Sadeghi, Bijan Nouri, Hadi Zare Marzouni.
Declaration of Conflicting Interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding: The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by the Research Deputy of Kurdistan University of Medical Sciences by code 1395.104.
Ethical Approval: Ethical approval was not required for this article as no human subjects were involved.
References
- 1. World Health Organization. Preventing Chronic Diseases: A Vital Investment. Geneva, Switzerland: World Health Organization; 2005. [Google Scholar]
- 2. Smeltzer SC, Bare BG, Hinkle JL, Cheever KH. Brunner and Suddarth’s Textbook of Medical Surgical Nursing. 12th ed London, England: Wolters Kluwer; 2010:205–231. [Google Scholar]
- 3. Kumar V, Abbas A, Aster J. Robbins Pathologic Basis of Disease. 9th ed Tehran, Iran: Arjomand; 2014. [Google Scholar]
- 4. Mousavi SM, Gouya MM, Ramazani R, Davanlou M, Hajsadeghi N, Seddighi Z. Cancer incidence and mortality in Iran. Ann Oncol. 2009;20:556–563. [DOI] [PubMed] [Google Scholar]
- 5. Rafieian-Kopaie M, Nasri H. On the occasion of World Cancer Day 2015: the possibility of cancer prevention or treatment with antioxidants: the Ongoing Cancer Prevention Researches. Int J Prev Med. 2015;6:108 doi:10.4103/2008-7802.169077. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Lachenmayer A, Alsinet C, Chang CY, Liovit JM. Molecular approaches to treatment of hepatocellular carcinoma. Dig Liver Dis. 2010;42:264–272. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Newman DJ, Cragg GM. Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2007;70:461–477. [DOI] [PubMed] [Google Scholar]
- 8. Mansouri E, Kooti W, Bazvand M, et al. The effect of hydro-alcoholic extract of Foeniculum vulgare Mill on leukocytes and hematological tests in male rats. Jundishapur J Nat Pharm Prod. 2015;10:e18396. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Kooti W, Ghasemiboroon M, Asadi-Samani M, et al. The effects of hydro-alcoholic extract of celery on lipid profile of rats fed a high fat diet. Adv Environ Biol. 2014;8:325–330. [Google Scholar]
- 10. Kooti W, Hasanzadeh-Noohi Z, Sharafi-Ahvazi N, Asadi-Samani M, Ashtary-Larky D. Phytochemistry, pharmacology, and therapeutic uses of black seed (Nigella sativa). Chin J Nat Med. 2016;14:732–745. [DOI] [PubMed] [Google Scholar]
- 11. Sakarkar DM, Deshmukh VN. Ethnopharmacological review of traditional medicinal plants for anticancer activity. Int J Pharm Tech Res. 2011;3:298–308. [Google Scholar]
- 12. Valastyan S, Weinberg RA. Tumor metastasis: molecular insights and evolving paradigms. Cell. 2011;147:275–292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Asadi-Samani M, Kooti W, Aslani E, Shirzad H. A systematic review of Iran’s medicinal plants with anticancer effects. J Evid Based Complementary Altern Med. 2016;21:143–153. [DOI] [PubMed] [Google Scholar]
- 14. Kooti W, Farokhipour M, Asadzadeh Z, Ashtary-Larky D, Asadi-Samani M. The role of medicinal plants in the treatment of diabetes: a systematic review. Electron Physician. 2016;8:1832–1842. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Kooti W, Ghasemiboroon M, Ahangarpoor A, et al. The effect of hydro-alcoholic extract of celery on male rats in fertility control and sex ratio of rat offspring. J Babol Univ Med Sci. 2014;16(4):43–49. [Google Scholar]
- 16. Kooti M, Ghasemiboroon M, Asadi-Samani M, et al. The effect of alcoholic extract of celery leaves on the delivery rate (fertilization and stillbirths), the number, weight and sex ratio of rat off spring. AENSI. 2014;8:824–830. [Google Scholar]
- 17. Kooti W, Mansouri E, Ghasemiboroon M, Harizi M, Ashtary-Larky D, Afrisham R. The effects of hydroalcoholic extract of Apium graveolens leaf on the number of sexual cells and testicular structure in rat. Jundishapur J Nat Pharm Prod. 2014;9:e17532. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Kooti W, Ahangarpoor A, Ghasemiboroon M, et al. Effect of Apium graveolens leaf extract on serum level of thyroid hormones in male rat. J Babol Univ Med Sci. 2014;16(11):44–50. [Google Scholar]
- 19. Ameh SJ, Tarfa FD, Ebeshi BU. Traditional herbal management of sickle cell anemia: lessons from Nigeria. Anemia. 2012;2012:607436 doi:10.1155/2012/607436. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Noori Ahmad Abadi M, Mortazavi M, Kalani N, Marzouni HZ, Kooti W, Ali-Akbari S. Effect of hydroalcoholic extract of Rosmarinus officinalis L. leaf on anxiety in mice. J Evid Based Complementary Altern Med. 2016;21:NP85–NP90. [DOI] [PubMed] [Google Scholar]
- 21. Khalighi-Sigaroodi F, Jeddi-Tehrani M, Ahvazi M, et al. Cytotoxicity evaluation of Taverniera spartea on human cancer cell lines. J Med Plants. 2014;2:114–128. [Google Scholar]
- 22. Dalali Isfahani L, Monajemi R, Amjad L. Cytotoxic effects of extract and essential oil leaves of Achillea wilhelmsii C. Koch on colon cancers cells. Exp Anim Biol. 2013;1(3):1–6. [Google Scholar]
- 23. Uddin SJ, Grice ID, Tiralongo E. Cytotoxic effects of Bangladeshi medicinal plant extracts. J Evid Based Complementary Altern Med. 2009;111:578092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Sharma H, Parihar L, Parihar P. Review on cancer and anticancerous properties of some medicinal plants. J Med Plant Res. 2011;5:1818–1835. [Google Scholar]
- 25. Azadbakht M, Semnani K, Khansari N. The essential oils composition of Achillea wilhelmsii C. Koch leaves and flowers. J Med Plan. 2003;2(6):55–59. [Google Scholar]
- 26. Dokhani SH, Cottrell T, Khajeddin J, Mazza G. Analysis of aroma and phenolic components of selected Achillea species. Plant Food Hum Nutr. 2005;60(2):55–62. [DOI] [PubMed] [Google Scholar]
- 27. Milner JA. A historical perspective on garlic and cancer. J Nutr. 2001;131(3 suppl):1027s–1031s. [DOI] [PubMed] [Google Scholar]
- 28. Thomson M, Ali M. Garlic (Allium sativum): a review of its potential use as an anti-cancer agent. Curr Cancer Drug Targets. 2003;3:67–81. [DOI] [PubMed] [Google Scholar]
- 29. Bianchini F, Vainio H. Allium vegetables and organosulfur compounds: do they help prevent cancer? Environ Health Perspect. 2001;109:893–902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Nakagawa H, Tsuta K, Kiuchi K, et al. Growth inhibitory effects of diallyl disulfide on human breast cancer cell lines. Carcinogenesis. 2001;22:891–897. [DOI] [PubMed] [Google Scholar]
- 31. Colic M, Vucevic D, Kilibarda V, Radicevic N, Savic M. Modulatory effects of garlic extracts on proliferation of T-lymphocytes in vitro stimulated with concanavalin A. Phytomedicine. 2002;9:117–124. [DOI] [PubMed] [Google Scholar]
- 32. Ahmed N, Laverick J, Sammons J, Zhang H, Maslin DJ, Hassan HT. Ajoene, a garlic-derived natural compound, enhances chemotherapy-induced apoptosis in human myeloid leukaemia CD34-positive resistant cells. Anticancer Res. 2001;21:3519–3529. [PubMed] [Google Scholar]
- 33. Al-Snafi AE. Chemical constituents and pharmacological activities of Ammi majus and Ammi visnaga—a review. Int J Pharm Ind Res. 2013;3:257–265. [Google Scholar]
- 34. Nemati F, Eslami Jadidi B, Talebi Darabi M. Investigation cytotoxic effects of Ammi maju extract on MCF-7and HeLa cancer cell line. J Anim Biol. 2013;5(3):59–66. [Google Scholar]
- 35. Shokoohinia Y, Hosseinzadeh L, Alipour M, Mostafaie A, Mohammadi-Motlagh HR. Comparative evaluation of cytotoxic and apoptogenic effects of several coumarins on human cancer cell lines: osthole induces apoptosis in p53-deficient H1299 cells. Adv Pharmacol Sci. 2014;2014:8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Vanachayangkul P, Byer K, Khan S, Butterweck V. An aqueous extract of Ammi visnaga fruits and its constituent’s khellin and visnagin prevent cell damage caused by oxalate in renal epithelial cells. Phytomedicine. 2010;17:653–658. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Ghareeb AM, Zedan TH, Gharb LA. Antibacterial and antifungal activities of Ammi visnaga extracts against pathogenic microorganisms. Iraqi J Sci. 2011;52:30–36. [Google Scholar]
- 38. Maleki D, Kyoomehr P, Rajabi A, Amin GR, Azizi E. Cytotoxic activity of Ammi visnaga (L.) Lam. against T47D (breast ductal carcinoma) cell line. North Khorasan Univ Med Sci. 2012. http://journals.nkums.ac.ir/index.php/ndnkh/article/viewFile/292/472. Accessed February 27, 2017.
- 39. Mohammed ZY, Nada SM, Al-Halbosiy MM, Abdulfattah SY, Abdul-Hameed B. Cytotoxic effects of Ammi visnaga volatile oil on some cancer cell lines. J Biotechnol Res Center. 2014;8(1):5–7. [Google Scholar]
- 40. Abduljalil TZ, Saour K, Nasser AMA. Phytochemical study of some flavonoids present in the fruits of two Ammi L. species wildly grown in Iraq. Iraqi J Pharm Sci. 2010;19(1):48–57. [Google Scholar]
- 41. Bora KS, Sharma A. The genus Artemisia: a comprehensive review. Pharm Biol. 2011;49:101–109. [DOI] [PubMed] [Google Scholar]
- 42. Gordanian B, Behbahani M, Carapetian J, Fazilati M. Cytotoxic effect of Artemisia absinthium L. grown at two different altitudes on human breast cancer cell line MCF7. Pajouhesh Dar Pezeshki. 2012;36:124–131. [Google Scholar]
- 43. Asgarpanah J, Ariamanesh A. Phytochemistry and pharmacological properties of Myrtus communis L. Indian J Tradit Knowledge. 2015;14:82–87. [Google Scholar]
- 44. Haghi G, Safaei A, Safai Ghomi J. Identification and determination of flavonoids in leaf, dried aqueous and dried hydroalcoholic extract of Artemisia absinthium by HPLC. Iran J Pharm Res. 2004;3(2):89–90. [Google Scholar]
- 45. Zhou HJ, Wang WQ, Wu GD, Lee JLA. Artesunate inhibits angiogenesis and down regulates vascular endothelial growth factor expression in chronic myeloid leukemia K562 cells. Vasc Pharmacol. 2007;47:131–138. [DOI] [PubMed] [Google Scholar]
- 46. Akrout A, Gonzalez LA, Hajer El J. Antioxidant and antitumor activities of Artemisia campestris and Thymelaea hirsuta from southern Tunisia. Food Chem Toxicol. 2011;49(2):342–47. [DOI] [PubMed] [Google Scholar]
- 47. Aldaghi L, DehpoorJoybari A, Nemati F, Mirdashti R, Akrami R. The effects of cytotoxicity of Astragalus cystosus on the HeLa cells by using MTT method. J Sabzevar Univ Med Sci. 2014;20:603–610. [Google Scholar]
- 48. Cassileth BR, Rizvi N, Deng G, et al. Safety and pharmacokinetic trial of docetaxel plus an Astragalus-based herbal formula for non-small cell lung cancer patients. Cancer Chemother Pharmacol. 2009;65:67–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Hu YW, Liu CY, Du CM, Zhang J, Wu WQ, Gu ZL. Induction of apoptosis in human hepatocarcinoma SMMC-7721 cells in vitro by flavonoids from Astragalus complanatus . J Ethnopharmacol. 2009;123:293–301. [DOI] [PubMed] [Google Scholar]
- 50. Abdolmohammadi MH, Fouladdel Sh, Shafiee A, Amin Gh, Ghaffari SM, Azizi E. Antiproliferative and apoptotic effect of Astrodaucus orientalis (L.) Drude on T47D human breast cancer cell line: Potential mechanisms of action. Afr J Biotechnol. 2009;8:4265–4276. [Google Scholar]
- 51. Razavi SM, Imanzadeh G, Dolati S, et al. Phytochemical prospection and biological activity of Astrodaucus orientalis (L.) Drude growing wild in Iran. Pharmacologia. 2011;2:299–301. [Google Scholar]
- 52. Nazemiyeh H, Razavi SM, Delazar A, et al. Distribution profile of volatile constituents in different parts of Astrodaucus orientalis (L.) Drude. Rec Nat Prod. 2009;3:126–130. [Google Scholar]
- 53. Sharaf M, El-Ansari MA, Saleh NA. New flavonoids from Avicennia marina . Fitoterapia. 2000;71:274–277. [DOI] [PubMed] [Google Scholar]
- 54. Momtazi Borojeni A, Behbahani M, Sadeghi-Aliabadi H. Evaluation of cytotoxic effect of some extracts of Avicennia marina against MDA-MB231 human breast cancer cell line. Pharm Sci. 2011;16:229–238. [Google Scholar]
- 55. Moussaieff A, Mechoulam R. Boswellia resin: review of in-vitro, in-vivo and clinical trials. J Pharm Pharmcol. 2009;61:1281–1293. [DOI] [PubMed] [Google Scholar]
- 56. Siddiqui MZ. Boswellia serrata, a potential antiinflammatory agent: an overview. Indian J Pharm Sci. 2011;73:255–261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57. Forouzandeh S, Naghsh N, Salimi S, Jahantigh D. Cytotoxic effect of Boswellia serrata hydroalcholic extract on human cervical carcinoma epithelial cell line. Med Lab J. 2014;8(1):7–13. [Google Scholar]
- 58. Chashoo G, Singh SK, Sharma PR, et al. A propionyloxy derivative of 11-keto-boswellic acid induces apoptosis in HL-60 cells mediated through topoisomerase I & II inhibition. Chem Biol Interact. 2011;189:60–71. [DOI] [PubMed] [Google Scholar]
- 59. Huang MT, Badmaev V, Ding Y, Liu Y, Xie JG, Ho CT. Anti-tumor and anti-carcinogenic activities of triterpenoid, beta-boswellic acid. Biofactors. 2000;13:225–230. [DOI] [PubMed] [Google Scholar]
- 60. Poeckel D, Werz O. Boswellic acids: biological actions and molecular targets. Curr Med Chem. 2006;13:3359–3369. [DOI] [PubMed] [Google Scholar]
- 61. Yasumoto R, Kawanishi H, Tsujino T, et al. Clinical evaluation of long-term treatment using cernitin pollen extract in patients with benign prostatic hyperplasia. Clin Ther. 1995;17:82–87. [DOI] [PubMed] [Google Scholar]
- 62. Adhami V, Ahmad N, Mukhtar H. Molecular targets for green tea in prostate cancer prevention. J Nutr. 2003;133:2417S–2424S. [DOI] [PubMed] [Google Scholar]
- 63. Carmen C, Reyes A, Rafael G. Beneficial effects of green tea—a review. J Am Coll Nutr. 2006;25:79–99. [DOI] [PubMed] [Google Scholar]
- 64. Mepur HR, Thiruverkadu SS, Clarence CM, et al. Epicatechins purified from green tea (Camellia sinensis) differentially suppress growth of gender-dependent human cancer cell lines. J Evid Based Complementary Altern Med. 2006;3:237–247. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65. Ravindranath MH, Ramasamy V, Moon S, Ruiz C, Muthugounder S. Differential growth suppression of human melanoma cells by tea (Camellia sinensis) epicatechins (ECG, EGC and EGCG). Evid Based Complement Alternat Med. 2009;6:523–530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66. Hosain Zadegan H, Ezzet Por B, Abdollah Por F, Motamedy M, Rashidipor M. Study of cytotoxic activity of olive and green tea extracts on breast tumor cell line. J Ardabil Univ Med Sci. 2010;10:287–294. [Google Scholar]
- 67. Wang Y, Duan H, Yang H. A case-control study of stomach cancer in relation to Camellia sinensis in China. Surg Oncol. 2015;24:67–70. [DOI] [PubMed] [Google Scholar]
- 68. Hussain AI, Rathore HA, Sattar MZ, Chatha SA, Sarker SD, Gilani AH. Citrullus colocynthis (L.) Schrad (bitter apple fruit): a review of its phytochemistry, pharmacology, traditional uses and nutritional potential. J Ethnopharmacol. 2014;155:54–66. [DOI] [PubMed] [Google Scholar]
- 69. Tavakkol Afshari J, Rakhshandeh H, Zamani AR, Mahdavi Shahri N, Ghazezadeh L, Norozi M. Cytotoxicity effects of Citrullus colocynthis on Hep2 and L929 cell lines. Hakim Res J. 2005;8(2):47–54. [Google Scholar]
- 70. Hatam NA, Whiting DA, Yousif NJ. Cucurbitacin glycosides from Citrullus colocynthis . Phytochemistry. 1876;28:1268–1271. [Google Scholar]
- 71. Wasfi IA. Some pharmacological studies on Citrullus colocynthis . J Herbs Spices Med Plants. 1994;2(2):65–79. [Google Scholar]
- 72. Ayyad SEN, Abdel-Lateff A, Alarif WM, Patacchioli FR, Badria FA, Ezmirly ST. In vitro and in vivo study of cucurbitacins-type triterpene glucoside from Citrullus colocynthis growing in Saudi Arabia against hepatocellular carcinoma. Environ Toxicol Pharmacol. 2012;33:245–251. [DOI] [PubMed] [Google Scholar]
- 73. Tannin-Spitz T, Grossman S, Dovrat S, Gottlieb HE, Bergman M. Growth inhibitory activity of cucurbitacin glucosides isolated from Citrullus colocynthis on human breast cancer cells. Biochem Pharmacol. 2007;73:56–67. [DOI] [PubMed] [Google Scholar]
- 74. Srivastava R, Ahmed H, Dixit RK, Saraf SA. Crocus sativus L. A comprehensive review. Pharmacogn Rev. 2010;4:200–208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75. Escribano J, Alonso GL, Coca-Prados M, Fernandez JA. Crocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitro. Cancer Lett. 1996;100(12):23–30. [DOI] [PubMed] [Google Scholar]
- 76. Abdullaev FI, Frenkle GD. Effect of saffron on cell colony formation and cellular nucleic acid and protein syntheses. Biofactors. 1992;3:201–204. [PubMed] [Google Scholar]
- 77. Aung HH, Wang CZ, Ni M, et al. Crocin from Crocus sativus possesses significant anti-proliferation effects on human colorectal cancer cells. Exp Oncol. 2007;29:175–180. [PMC free article] [PubMed] [Google Scholar]
- 78. Mousavi M, Baharara J, Asadi-Samani M. Anti-angiogenesis effect of Crocous sativus L. extract on matrix metalloproteinase gene activities in human breast carcinoma cells. J Herb Med Pharmacol. 2014;3:101–105. [Google Scholar]
- 79. Abdullaev FI, Frenkel GD. The effect of saffron on intracellular DNA, RNA and protein synthesis in malignant and non-malignant human cells. Biofactors. 1991;4:43–45. [PubMed] [Google Scholar]
- 80. Rahimifard N, Haji Mahdipour H, Hedayati MH, Esmaili M. Evaluation of cytotoxic effects of aqueous-methanolic saffron extract on Vero, HeLa and Hep2 cell lines using MTT assay method. Iran J Med Microbiol. 2011;4(4):59–65. [Google Scholar]
- 81. Tavakkol-Afshari J, Brook A, Mousavi SH. Study of cytotoxic and apoptogenic properties of saffron extract in human cancer cell lines. Food Chem Toxicol. 2008;46:3443–3447. [DOI] [PubMed] [Google Scholar]
- 82. Fallah Huseini H, Zahmatkash M, Haghighi M. A review on pharmacological effects of Curcuma longa L. (turmeric). JMP. 2010;1(33):1–15. [Google Scholar]
- 83. Ayyadurai1 N, Valarmathy N, Kannan S, Jansirani D, Alsenaidy A. Evaluation of cytotoxic properties of Curcuma longa and Tagetes erecta on cancer cell line (Hep2). Afr J Pharm Pharmacol. 2013;7:736–739. [Google Scholar]
- 84. Ranjbari J, Alibakhshi A, Arezumand R, et al. Effects of Curcuma longa extract on telomerase activity in lung and breast cancer cells. Zahedan J Res Med Sci. 2014;16(10):1–6. [Google Scholar]
- 85. Mohammad P, Nosratollah Z, Mohammad R, Abbas A, Javad R. The inhibitory effect of Curcuma longa extract on telomerase activity in A549 lung cancer cell line. Afr J Biotechnol. 2010;9(6). http://www.ajol.info/index.php/ajb/article/view/78098. Accessed February 27, 2017. [Google Scholar]
- 86. Hosseinimehr SJ. A review of preventive and therapeutic effects of curcumin in patients with cancer. J Clin Excellence. 2014;2(2):50–63. [Google Scholar]
- 87. Anand P, Sundaram C, Jhurani S, Kunnumakkara AB, Aggarwal BB. Curcumin and cancer: an “old-age” disease with an “age old” solution. Cancer Lett. 2008;267:133–164. [DOI] [PubMed] [Google Scholar]
- 88. Calabrese V, Bates TE, Mancuso C, et al. Curcumin and the cellular stress response in free radical-related diseases. Mol Nutr Food Res. 2008;52:1062–1073. [DOI] [PubMed] [Google Scholar]
- 89. Shafaghati N, Hedayati N, Hosseinimehr SJ. Protective effects of curcumin against genotoxicity induced by 131-iodine in human cultured lymphocyte cells. Pharmacogn Mag. 2014;10(38):106–110. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90. Sharma RA, Gescher AJ, Steward WP. Curcumin: the story so far. Eur J Cancer. 2005;41:1955–1968. [DOI] [PubMed] [Google Scholar]
- 91. Sarkar FH, Li Y, Wang Z, Padhye S. Lesson learned from nature for the development of novel anti-cancer agents: implication of isoflavone, curcumin, and their synthetic analogs. Curr Pharm Des. 2010;16:1801–1812. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92. Sadooghi SD, Nezhad-Shahrokh-Abadi KH, Zafar Balanezhad S, Baharara J. Investigating the cytotoxic effects of ethanolic extract of Ferula assa-foetida resin on HepG2 cell line. Feyz. 2013;17:323–330. [Google Scholar]
- 93. Guo C, Yang J. Antioxidant activities of Ferula assa-foetida as determined by FRAP assay. Nutr Res. 2003;23:1719–1726. [Google Scholar]
- 94. Hofbauer R, Frass M, Gmeiner B, Kaye AD, Frost EA. Effects of Ferula assa-foetida extract on neutrophil migration at the cellular level. Heart Dis. 2001;3(1):14–17. [DOI] [PubMed] [Google Scholar]
- 95. Escribano J, Alonso GL. Crocin, sofranol and picocrocine from Ferula assa-foetida inhibit the growth of human cancer cell in vitro. Cancer Lett. 1996;100(12):23–30. [DOI] [PubMed] [Google Scholar]
- 96. Nakagawa H, Tsuta K, Kiuchi K, et al. Growth inhibitory effects of diallyl disulfide on human breast cancer cell lines. Carcinogenesis. 2001;22:891–897. [DOI] [PubMed] [Google Scholar]
- 97. Valiahdi SM, Iranshahi M, Sahebkar A. Cytotoxic activities of phytochemicals from Ferula species. Daru J Pharm Sci. 2013;21:39–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 98. Khanahmadi MM, Naghdi Badi H, Akhondzadeh S, et al. A review on medicinal plant of Glycyrrhiza glabra L. JMP. 2013;2(46):1–12. [Google Scholar]
- 99. Hamta A, Shariatzadeh SMA, Soleimani Mehranjani SMA, Fallah Huseini H, Hosseinabadi F. The cytotoxic effects of Glycyrrhiza glabra L. root extract on 4T1 cell line derived from BALB/c mice mammary tumors. J Med Plant. 2014;2(50):92–103. [Google Scholar]
- 100. Harwansh RK, Patra KC, Pareta SK, Singh J. Pharmacological studies on Glycyrrhiza glabra. Pharmacologyonline. 2011;2:1032–1038. [Google Scholar]
- 101. Baltina LA. Chemical modification of glycyrrhizic acid as a route to new bioactive compounds for medicine. Curr Med Chem. 2003;10:155–171. [DOI] [PubMed] [Google Scholar]
- 102. Rossi T, Castelli M, Zandomeneghi G, Ruberto A, Benassi L, Magnoni C. Selectivity of action of glycyrrhizin derivatives on the growth of MCF-7 and HEP-2 cells. Anticancer Res. 2003;23(5A):3813–3818. [PubMed] [Google Scholar]
- 103. Nourazarian SM, Nourazarian A, Majidinia M, Roshaniasl E. Effect of root extracts of medicinal herb Glycyrrhiza glabra on HSP90 gene expression and apoptosis in the HT-29 colon cancer cell line. Asian Pac J Cancer Prev. 2015;16:8563–8566. [DOI] [PubMed] [Google Scholar]
- 104. Shokrzadeh M, Parvaresh A, Shahani S, Habibi E, Zalzar Z. Cytotoxic effects of Lagenaria siceraria Standl. extract on cancer cell line. J Mazand Univ Med Sci. 2013;23(97):225–230. [Google Scholar]
- 105. Saha P, Kundu Sen S, Bala A, Mazumder UK, Haldar PK. Evaluation of anticancer activity of Lagenaria siceraria aerial parts. Int J Cancer. 2011;3:244–253. [Google Scholar]
- 106. Ghosh K, Chandra K, Ojha AK, Sarkar S, Islam SS. Structural identification and cytotoxic activity of a polysaccharide from the fruits of Lagenaria siceraria (Lau). Carbohydr Res. 2009;344:693–698. [DOI] [PubMed] [Google Scholar]
- 107. Tyagi N, Sharma G, Hooda V. Phytochemical and pharmacological profile of Lagenaria siceraria: an overview. Int Res J Pharm. 2012;3(3):1–4. [Google Scholar]
- 108. Shah B, Seth A. Pharmacognostic studies of the Lagenaria siceraria (molina) Standley. Int J Pharm Tech Res. 2010;2:121–124. [Google Scholar]
- 109. Raval ND, Pandya TN. Pharmacognostic study of Lepidium sativum Linn (Chandrashura). Ayu. 2011;32:116–119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110. Al-Fatimi M, Friedrich U, Jenett-Siems K. Cytotoxicity of plants used in traditional medicine in Yemen. Fitoterapia. 2005;76:355–358. [DOI] [PubMed] [Google Scholar]
- 111. Aslani E, Naghsh N, Ranjbar M. Cytotoxic effects of hydro-alcoholic extracts of cress (Lepidium sativum)—made from different stages of the plant—on k562 Leukemia cell line. Hormozgan Med J. 2015;18:411–419. [Google Scholar]
- 112. Mahassni SH, Al-Reemi RM. Apoptosis and necrosis of human breast cancer cells by an aqueous extract of garden cress (Lepidium sarivum) seeds. Saudi J Biol Sci. 2013;20:131–139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 113. Servatyari K, Ahmadi A, Kashefi H, Menbari MN, Rostami R, Moloudi MR. The effects of hydroalcoholic extract of Medicago sativa on liver functional test, blood biochemical and coagulation system parameters in male rat. Sci J Kurdistan Univ Med Sci. 2017;21(6):16–26. https://sjku.muk.ac.ir/article-1-2819-en.pdf. Accessed February 27, 2017. [Google Scholar]
- 114. Huyghe C, Bertin E, Landry N. Medicinal and nutraceutical uses of alfalfa (Medicago sativa L). A review In: Acharya SN, Thomas JE, eds. Advances in Medicinal Plant Research. Trivandrum, India: Research Signpost; 2007:147–172. [Google Scholar]
- 115. Singh Bora K, Sharma A. Phytochemical and pharmacological potential of Medicago sativa: a review. Pharm Biol. 2011;49:211–220. [DOI] [PubMed] [Google Scholar]
- 116. Aslani E, Naghsh N, Ranjbar M. Cytotoxic effect of Mentha pulegium plants before flowering on human chronic myelogenous leukemia K562 cancer category. J Arak Univ Med Sci. 2014;16(10):1–10. [Google Scholar]
- 117. Vian MA, Fernandez X, Visinoni F, Chemat F. Microwave hydrodiffusion and gravity, a new technique for extraction of essential oils. J Chromatogr A. 2008;1190(1):14–17. [DOI] [PubMed] [Google Scholar]
- 118. Alipour G, Dashti S, Hosseinzadeh H. Review of pharmacological effects of Myrtus communis L. and its active constituents. Phytother Res. 2014;28:1125–1136. [DOI] [PubMed] [Google Scholar]
- 119. Ogur R. Studies with Myrtus communis L.: anticancer properties. J Intercult Ethnopharmacol. 2014;3:135–137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 120. Sumbul S, Ahmad MA, Asif M, Akhtar M. Myrtus communis Linn—a review. Indian J Nat Prod Resour. 2011;2:395–402. [Google Scholar]
- 121. Mothana RA, Kriegisch S, Harms M, Wende K, Lindequist U. Assessment of selected Yemeni medicinal plants for their in vitro antimicrobial, anticancer, and antioxidant activities. Pharm Biol. 2011;49:200–210. [DOI] [PubMed] [Google Scholar]
- 122. Asgarpanah J, Ariamanesh A. Phytochemistry and pharmacological properties of Myrtus communis L. Indian J Tradit Knowledge. 2015;14:82–87. [Google Scholar]
- 123. Tretiakova I, Blaesius D, Maxia L, et al. Myrtucommulone from Myrtus communis induces apoptosis in cancer cells via the mitochondrial pathway involving caspase-9. Apoptosis. 2008;13:119–131. [DOI] [PubMed] [Google Scholar]
- 124. Tabasi NS, Khajavi-Rad A, Mahmoudi M, et al. The effects of Nigella sativa ethanolic extract on proliferation and apoptosis of renal cell carcinoma ACHN cell line. J Shahrekord Univ Med Sci. 2010;12(3):7–14. [Google Scholar]
- 125. Asadi-Samani M, Kafash-Farkhad N, Azimi N, Fasihi A, Alinia-Ahandani E, Rafieian-Kopaei M. Medicinal plants with hepatoprotective activity in Iranian folk medicine. Asian Pac J Trop Biomed. 2015;5:146–157. [Google Scholar]
- 126. Ait Mbarek L, Ait Mouse H, Elabbadi N, et al. Anti-tumor properties of blackseed (Nigella sativa L.) extracts. Braz J Med Biol Res. 2007;40:839–847. [DOI] [PubMed] [Google Scholar]
- 127. Gali-Muhtasib H, Diab-Assaf M, Boltze C, et al. Thymoquinone extracted from black seed triggers apoptotic cell death in human colorectal cancer cells via a p53-dependent mechanism. Int J Oncol. 2004;25:857–866. [PubMed] [Google Scholar]
- 128. Shoeib AM, Elgayyar M, Dudrich P, Bell J. In vitro inhibition of growth and induction of apoptosis in cancer cell lines by thymoquinone. Int J Oncol. 2003;22:107–113. [PubMed] [Google Scholar]
- 129. Muhtasib H, Roessner A, Schneider R. Thymoquinone: a promising anti-cancer drug form natural sources. Int J Biochem Cell Biol. 2006;38:1249–1253. [DOI] [PubMed] [Google Scholar]
- 130. Khalife R, Hodroj MH, Fakhoury R, Rizk S. Thymoquinone from Nigella sativa seeds promotes the antitumor activity of noncytotoxic doses of topotecan in human colorectal cancer cells in vitro. Planta Med. 2016;82:312. [DOI] [PubMed] [Google Scholar]
- 131. Elkady AI, Hussein RA, El-Assouli SM. Mechanism of action of Nigella sativa on human colon cancer cells: the suppression of AP-1 and NF-κB transcription factors and the induction of cytoprotective genes. Asian Pac J Cancer Prev. 2015;16:7943–7957. [DOI] [PubMed] [Google Scholar]
- 132. Ghanbari R, Anwar F, Alkharfy KM, Gilani AH, Saari N. Valuable nutrients and functional bioactives in different parts of olive (Olea europaea L.)—a review. Int J Mol Sci. 2012;13:3291–3340. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 133. Fini L, Hotchkiss E, Fogliano V, et al. Chemopreventive properties of pinoresinol-rich olive oil involve a selective activation of the ATM-p53 cascade in colon cancer cell lines. Carcinogenesis. 2008;29:139–146. [DOI] [PubMed] [Google Scholar]
- 134. Menendez JA, Vazquez-Martin A, Oliveras-Ferraros C, et al. Extra-virgin olive oil polyphenols inhibit HER2 (erbB-2)-induced malignant transformation in human breast epithelial cells: relationship between the chemical structures of extra-virgin olive oil secoiridoids and lignans and their inhibitory activities on the tyrosine kinase activity of HER2. Int J Oncol. 2009;34:43–51. [PubMed] [Google Scholar]
- 135. Rub M, Juliana C, Elvira I, Hern V, Ruiz-Gutierrez M, Luisa N. Acidic triterpenes compromise growth and survival of 20 astrocytoma cell lines by regulating reactive oxygen species accumulation. Cancer Res. 2007;67:3741–3751. [DOI] [PubMed] [Google Scholar]
- 136. Forouzandeh S, Naghsh N, Salimi S, Jahantigh D. Cytotoxic effect of Boswellia serrata hydroalcholic extract on human cervical carcinoma epithelial cell line. Med Lab J. 2014;8:7–13. [Google Scholar]
- 137. Jimenez J, Rivero NL, Rodrıguez R. Cytotoxicity of the b-carboline alkaloids harmine and harmaline in human cell assays in vitro. Exp Mol Pathol. 2008;60:381–389. [DOI] [PubMed] [Google Scholar]
- 138. Torabzadeh P, Dezfulian M. Study of cytotoxisity effects of aqueous extract of Physalis alkekengi against u937 cell line. Q J Anim Physiol Dev. 2013;6(4):15–25. [Google Scholar]
- 139. Li X, Zhao J, Yang M, et al. Physalins and withanolides from the fruits of Physalis alkekengi L. var. franchetii (Mast.) Makino and the inhibitory activities against human tumor cells. Phytochem Lett. 2014;10:95–100. [Google Scholar]
- 140. Banazadeh H, Delazar A, Habibi Roudkenar M, Rahmati Yamchi M, Sadeghzadeh Oscoui B, Mehdipour A. Effects of knotweet or Polygonum aviculare herbal extract on proliferation of HeLa cell line. Med J Mashad Univ Med Sci. 2012;54:238–241. [Google Scholar]
- 141. Mohammad R, Hossein B, Davood F, Farnaz T, Ali F, Yuse R. The apoptotic and cytotoxic effects of Polygonum avicular extract on HeLa-S cervical cancer cell line. Afr J Biochem Res. 2011;5:373–378. [Google Scholar]
- 142. Habibi RM, Mohammadi RA, Delazar A, et al. Effects of Polygonum aviculare herbal extract on proliferation and apoptotic gene expression of MCF-7. DARU. 2011;19:326–331. [PMC free article] [PubMed] [Google Scholar]
- 143. Salama HMH, Marraiki N. Antimicrobial activity and phytochemical analyses of Polygonum aviculare L. (Polygonaceae), naturally growing in Egypt. Saudi J Biol Sci. 2010;17:57–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 144. Zamiri-Akhlaghi A, Rakhshandeh H, Tayarani-Najaran Z, Mousavi SH. Study of cytotoxic properties of Rosa damascena extract in human cervix carcinoma cell line. Avicenna J Phytomed. 2011;1:74–77. [Google Scholar]
- 145. Khatib H, Rezaei-Tavirani M, Keshel SH, et al. Flow cytometry analysis of Rosa damascena effects on gastric cancer cell line (MKN45). Iran J Cancer Prev. 2013;6:30–36. [Google Scholar]
- 146. Gazák R, Walterová D, Kren V. Silybin and silymarin—new and emerging applications in medicine. Curr Med Chem. 2007;14:315–338. [DOI] [PubMed] [Google Scholar]
- 147. Shariatzadeh SMA, Hamta A, Soleimani M, Fallah Huseini H, Samavat S. The cytotoxic effects of silymarin on the 4T1 cell line derived from BALB/c mice mammary tumors. J Med Plants. 2014;4(52):55–65. [Google Scholar]
- 148. Khazir J, Mir BA, Mir SA, Cowan D. Natural products as lead compounds in drug discovery. J Asian Nat Prod Res. 2013;15:764–788. [Google Scholar]
- 149. Hamta A, Parvini P. Study of cytotoxic effects of taxol and rosemary extracts on cancerous cells derived from DMBA-induced breast cancer in SD rats. Cell Tissue Res. 2011;2:117–126. [Google Scholar]
- 150. Sadeghi-Aliabadi H, Alavi M, Asghari GH, Mirian M. Cytotoxic evaluation of different extracts of Taxus baccata against MDA-MB-468, HeLa and K562 cancer cell lines. J Isfahan Med Sch. 2013;31:1508–1517. [Google Scholar]
- 151. Sabzali S, Arman R, Panahi J, Havasian MR, Haghani K, Bakhtiyari S. Investigation on the inhibitory effects of hydro-alcoholic extract of Thymbra spicata on the growth of lung cancer cell line SK-Mes-1. J Ilam Univ Med Sci. 2014;22:153–158. [Google Scholar]
- 152. Dirican E, Turkez H, Toğar B. Modulatory effects of Thymbra spicata L. different extracts against the mercury induced genotoxicity in human lymphocytes in vitro. Cytotechnology. 2012;64:181–186. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 153. Keramati K, Sanai K, Babakhani A, Rakhshan M, Vaezi GH, Haeri A. Effect of hydroalcoholic extract Thymus vulgaris induced prostate cancer injection DMBA in Wistar rats. J Pazhuhesh. 2011;35:135–140. [Google Scholar]
- 154. Sertel S, Eichhorn T, Plinkert PK, Efferth T . Cytotoxicity of Thymus vulgaris essential oil towards human oral cavity squamous cell carcinoma. Anticancer Res. 2011;31:81–87. [PubMed] [Google Scholar]
- 155. Keeforer-Ring K, Thompson JD, Linhart YB. Beyond six scents: defining a seventh Thymus vulgaris chemotype new to southern France by ethanol extraction. Flavour Frag J. 2009;24:117–122. [Google Scholar]
- 156. Abaza MS, Orabi KY, Al-Quattan E, Al-Attiyah RJ. Growth inhibitory and chemo-sensitization effects of naringenin, a natural flavanone purified from Thymus vulgaris, on human breast and colorectal cancer. Cancer Cell Int. 2015;24:15–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 157. Al-Menhali A, Al-Rumaihi A, Al-Mohammed H, et al. Thymus vulgaris (thyme) inhibits proliferation, adhesion, migration, and invasion of human colorectal cancer cells. J Med Food. 2015;18:54–59. [DOI] [PubMed] [Google Scholar]
- 158. Ulbricht C, Basch E, Burke D, et al. Fenugreek (Trigonella foenum-graecum L. Leguminosae): an evidence-based systematic review by the natural standard research collaboration. J Herb Pharmacother. 2007;7:143–177. [DOI] [PubMed] [Google Scholar]
- 159. Alsemari A, Alkhodairy F, Aldakan A, et al. The selective cytotoxic anti-cancer properties and proteomic analysis of Trigonella foenum-graecum . BMC Complement Alternat Med. 2014;14:114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 160. Amin A, Alkaabi A, Al-Falasi S, Daoud SA. Chemopreventive activities of Trigonella foenum graecum (fenugreek) against breast cancer. Cell Biol Int. 2005;29:687–694. [DOI] [PubMed] [Google Scholar]
- 161. Hasanzadeh E, Rezazadeh SH, Shamsa SF, Dolatabadi R, Zarringhalam J. Review on phytochemistry and therapeutic properties of fenugreek (Trigonella foenum-graceum). J Med Plants. 2010;2(34):1–18. [Google Scholar]
- 162. Sur P, Das M, Gomes A, et al. Trigonella foenum graecum (fenugreek) seed extract as an antineoplastic agent. Phytother Res. 2001;15:257–259. [DOI] [PubMed] [Google Scholar]
- 163. Joshi BC, Mukhija M, Kalia AN. Pharmacognostical review of Urtica dioica L. IJGP. 2014;8:201–209. [Google Scholar]
- 164. Durak I, Biri H, Devrim E, Sözen S, Avcı A. Aqueous extract of Urtica dioica makes significant inhibition on adenosine deaminase activity in prostate tissue from patients with prostate cancer. Cancer Biol Ther. 2004;3:855–857. [DOI] [PubMed] [Google Scholar]
- 165. Konrad L, Müller HH, Lenz C, Laubinger H, Aumüller G, Lichius JJ. Antiproliferative effect on human prostate cancer cells by a stinging nettle root (Urtica dioica) extract. Planta Med. 2000;66:44–47. [DOI] [PubMed] [Google Scholar]
- 166. Safarinejad MR. Urtica dioicafor treatment of benign prostatic hyperplasia: a prospective, randomized, double-blind, placebo-controlled, crossover study. J Herb Pharmacother. 2005;5(4):1–11. [PubMed] [Google Scholar]
- 167. Aydin M, Aslaner A, Zengin A. Using Urtica dioica in esophageal cancer: a report of a case. Internet J Surg. 2006;7(2). https://print.ispub.com/api/0/ispub-article/9543. Accessed February 27, 2017. [Google Scholar]
- 168. Konrad L, Müller HH, Lenz C, Laubinger H, Aumüller G, Lichius JJ. Antiproliferative effect on human prostate cancer cells by a stinging nettle root (Urtica dioica) extract. Planta Med. 2000;66:44–47. [DOI] [PubMed] [Google Scholar]
- 169. Khazaei Poul Y, Majd A, Labibi F, Moini Zanjani T. Cytotoxic effect of methanolic extracts of vegetative and reproductive parts of Vinca rosea on A431, a human skin squamous carcinoma cell line. J Physiol Pharmacol. 2014;18:364–372. [Google Scholar]
- 170. Roepkea J, Salima V, Wua M, et al. Vinca drug components accumulate exclusively in leaf exudates of Madagascar periwinkle. Proc Natl Acad Sci U S A. 2010;107:15287–15299. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 171. Siddiqui S, Ismail Z, Saidan N. Simultaneous determination of secondary metabolites from Vinca rosea plant extractives by reverse phase high performance liquid chromatography. Pharmacogn Mag. 2011;7(26):92–96. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 172. Jayakumar D, Mary SJ, Santhi RJ. Evaluation of antioxidant potential and antibacterial activity of Calotropis gigantea and Vinca rosea using in vitro model. Indian J Sci Technol. 2010;3:720–723. [Google Scholar]
- 173. Mortazavian SM, Ghorbani A, Ghorbani Hesari T. Effect of hydro-alcoholic extracts of Viola tricolor and its fractions on proliferation of cervix carcinoma cells. Iran J Obstet Gynecol Infertil. 2012;15(22):9–16. [Google Scholar]
- 174. Saether O, Craik DJ, Campbell ID, Sletten K, Juul J, Norman DG. Elucidation of the primary and three-dimensional structure of the uterotonic polypeptide kalata B1. Biochemistry. 1995;34:4147–4158. [DOI] [PubMed] [Google Scholar]
- 175. Vukics V, Kery A, Bonn GK, Guttman A. Major flavonoid components of heartsease (Viola tricolor L.) and their antioxidant activities. Anal Bioanal Chem. 2008;390:1917–1925. [DOI] [PubMed] [Google Scholar]
- 176. Kanadaswami C, Lee L, Lee PP, et al. The antitumor activities of flavonoids. In Vivo. 2005;19:895–910. [PubMed] [Google Scholar]
- 177. Marx WM, Teleni L, McCarthy AL, et al. Ginger (Zingiber officinale) and chemotherapy-induced nausea and vomiting: a systematic literature review. Nutr Rev. 2013;71:245–254. [DOI] [PubMed] [Google Scholar]
- 178. Moheghi N, Tavakkol Afshari J, Brook A. The cytotoxic effect of Zingiber officinale in breast cancer (MCF7) cell line. Ofogh-e-Danesh. GMUHS J. 2011;17(3):28–34. [Google Scholar]
- 179. Rahman S, Salehin F, Iqbal A. In vitro antioxidant and anticancer activity of young Zingiber officinale against human breast carcinoma cell lines. BMC Complement Alternat Med. 2011;11:76. [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]