Phytochemicals as Potential Anticancer Drugs: Time to Ponder Nature's Bounty

Abstract

Medicinal plants have been used from the beginning of human civilization, which is mostly evident from the ancient script and traditional herbal medicine recipe. Despite the historically enriched demonstration about the use of plant as therapeutics, the pharmaceutical industries lack interest on phytochemical research compared with synthetic drug. Mostly, the absence of information about plant-based medicinal therapeutics is responsible to draw the attention of researchers to think about natural products as potential drug for detrimental diseases, such as cancer. This review will cover about clinically successful plant-based anticancer drugs and underappreciated, but potential, drugs to bridge the information gap between plant biologists and clinical researchers. Additionally, unprecedented advancement of synthetic chemistry, omics study to pin point the target genes/proteins, and efficient drug delivery system have made it easier for researchers to develop a phytochemical as an efficient anticancer drug.

1. Introduction

Undoubtedly, we are living in a time when cancer is epidemic and one of the medical challenges of this century. Statistically, it is a devastating number to deal. According to the Cancer Research UK, 17 million new cases had been reported, and among them, 9.6 million patients ended up to death in 2018. If it continues in such a rate, by 2040, there will be 27.5 million new cancer patient each year. At the same time, if we wonder, how far we came to cure cancer—forget about that—because our understanding about cancer is like looking at the White House from the international space station, where we certainly do not realize the color or the power of the stuff we are looking at. However, if we take a step back before meddling our mind with thousands of target genes, proteins, and possible or probable drugs, the fundamental idea of different types of cancer is “uncontrolled cell division” [1]. In short, cell division is a rudimentary process from the very beginning of the existence of life in the universe. Symmetric cell division leads to proliferation and asymmetric cell division is an informative step for differentiation. It has been reported that uncontrolled symmetric cell division is the major factor for causing cancer [2]. It is quite reasonable to aim anticancer drugs to control the cell cycle machineries [3]. In recent years, along with the effort of traditional anticancer drug discovery approaches, which is time-consuming and expensive, there is a search for anticancer drug from plant-derived bioactive compounds. Furthermore, drug discovery and development from plant-based compounds are also inexpensive compared with conventional synthetic compounds [4].

The plants are visibly an efficient provider of food and shelter, but the role of plants as a source of medicine is underappreciated. Human civilization is using plant as a source of food, shelter, and medicine for almost same time [5]. The contribution of plant as medicine was neglected due to the lack of precise biochemical and pharmacological mechanisms. Surprisingly, in nature, plants are continuously and extensively exposed to natural pollutants, carcinogens, and toxic metals [6–9] compared with human. Apart from the classic crown gall disease [10], the example of uncontrolled cell division in plant is insignificant compared with the animal system. At the same time, plants synthesize divergent of secondary metabolites, mostly used for their defense and response to environmental cues, such as biotic and abiotic stresses [11–14]. In most of the cases, we have limited idea how plants tightly regulate their cell cycle machineries endogenously even after enormous exposure to hazardous components. Till date, several plant-derived compounds such as taxol [15], vinblastine [16], topotecan [17], and many more have been used as anticancer drugs successfully in clinical studies.

In this review, the existing successful plant-based anticancer drugs will be explored first and then the future direction of this emerging area and how the advancement of drug delivery system and cell type-specific production of anticancer drugs will uplift plant-based compounds as anticancer agents will be discussed.

2. Plant-Based Cancer Treatment

2.1. Looking Back to the Past to Find the Future

The most ancient text described the use of plant material as medicine was found in the Sumerian clay slab from Nagpur, India, and written approximately 5000 years ago. It contains information about using recent days' popular poppy, henbane, and mandrake as therapeutics [18]. Next, oldest evidence of medicinal plant was demonstrated in ancient Chinese literature written by Emperor Shen Nung circa 2500 BC [19, 20]. In a continuous historical effort, Theophrastus, known as “the father of botany,” first established the botanical science, documented in his book “De Causis Plantarum,” and classified several hundred medicinal plants [21, 22]. In addition, historically prominent Greek physician, pharmacologist, and botanist Pedanius Dioscorides wrote a 5-volume book, “De Materia Medica,” on the medicinal use of plant [23]. His book and research were enormously successful, and he was hired by Roman army as a physician. The legacy of Roman Empire on medicinal plant study was further carried by Muslim scholars during the Islamic Golden Age. For instance, Islamic scholar Ibn Baitar described more than thousand medicinal plants in his book, “Liber Magnae Collectionis Simplicum Alimentorum Et Medicamentorum” [24]. The knowledge of medicinal plants from ancient literature and text came to light through Carl Linnaeus's classification system, described in his book “Species Plantarum” [25].

In the early 19^th century, the advent of advanced synthetic chemistry helps us to decipher the mechanism, isolation and synthesis of active compounds from popular medicinal plants, such as poppy, ipecacuanha, strychnos, quinine, and pomegranate [26]. Despite the enriched history and success of medicinal plants, during the late 19^th and early 20^th centuries, the research on medicinal plant did not progress as it was supposed to. The reluctance of pharmaceutical industries about plant-based components caused a significant shift of focus from plant to synthetic chemistry on drug development [27].

Fortunately, the gear has been shifted in recent years. In 2015, the Nobel Prize in physiology and medicine was awarded to Tu Youyou for her discovery of artemisinin and dihydroartemisinin as antimalarial drug and highlight of the importance of plant-based components as a potentially powerful source of drug discovery. During the Vietnam War, Ho Chi Minh urged to develop antimalarial drugs for his soldiers. Tu Youyou became the part of that project to find the antimalarial treatment, and she screened over 2,000 traditional herbal medicines and discovered Artemisia annua recipe [28].

The success story of antimalarial drug based on traditional herbal medicine is not an isolated story; rather, it is a tiny part of plant-based arsenal as potential drugs. As a result, the significant effort on finding therapeutic agents for cancer treatment has been focused on plant-based compounds by the National Cancer Institute (NCI), USA. NCI-initiated Cancer Moonshot^SM project, aimed to accelerate the cancer research by making more cancer therapeutics available for patients, is focused on phytochemicals. As a part of this project, they have established a repertoire of natural products, and their purified chemical components to make them available for researchers to find new anticancer drugs.

Till date, several plant-based compounds have been reported for their anticancer activity, and among them, a good number of compounds is clinically successful as well. I have tried to summarize some important phytochemicals as potential anticancer drugs in Table 1 and Section 2.2.

Table 1.

Known phytochemicals, their source, and therapeutic use.

Phytochemical	Source	Therapeutic use	Reference
5-Fluorouracil	Withania somnifera	Human cervical cancer cell	[29]
Vindesine	Catharanthus roseus	Leukemias, testicular, breast and lung cancer	[30]
Vincristine	Catharanthus roseus	Lymphocytic leukemia	[30]
Vinblastine	Catharanthus roseus	Lymphocytic leukemia	[30]
Colchicine	Colchicum autumnale	Multiple solid tumors	[31]
Larotaxel	Taxus baccata	Breast, bladder, and pancreatic cancer	[32]
Cabazitaxel	Taxus baccata	Prostate cancer	[33]
Paclitaxel	Taxus brevifolia	Breast and ovarian cancer	[30]
Bullatacin	Annona squamosa	Liver cancer	[34]
Bryophyllin A	Bryophyllum pinnatum	Cervical cancer	[35]
Harmine	Peganum harmala	Breast cancer	[36]
Artemisinin	Artemisia annua	Liver, breast, and pancreatic cancer	[37]
Tannins	Debregeasia saeneb	Internal tumors	[38]
Theabrownin	Camellia sinensis	Lung cancer	[39]
Solamargine	Solanum nigrum	Breast, liver, lung, and skin cancer	[40]
Psoralidin	Psoralea corylifolia	Stomach and prostate cancer	[41]
Xanthatin	Xanthium strumarium	Lymphocytic leukemia and liver cancer	[42]
Thymoquinone	Nigella sativa	Colon, prostate, breast, and pancreas cancer	[43]
Kaempferol galactoside	Bauhinia variegata	Breast, lung, and liver cancer	[43]
Withaferin A, D	Withania somnifera	Breast, cervix, prostate, and colon cancer	[44]
Ginger	Zingiber officinale	Ovary, cervix, colon, liver, and urinary caner	[45]
Silibinin	Sylibum marianum	Lung, liver, skin, colon, and prostate cancer	[46]
Luteolin	Capsicum annuum	Colorectal cancer	[47]
Colchicine	Colchicum autumnale	Hodgkin's lymphoma, chronic granulocytic leukemia	[48]
Skimmianine	Aegle marmelos	Liver cancer	[49]
Boswellic acid	Boswellia serrata	Prostate cancer	[50]
Silymarin	Sylibum marianum	Colorectal cancer and colon cancer	[51]
Curcumin	Curcuma longa	Colon adenocarcinoma	[52]
Podophyllotoxin	Podophyllum peltatum	Non-small-cell lung carcinoma	[53]
Andrographolide	Andrographis paniculata	Colon cancer	[47]
Podophyllotoxin	Podophyllum hexandrum	Breast, ovary, lung, liver, bladder, and testis cancer	[54]
Betulinic acid	Betula utilis	Melanomas	[55]
Panaxadiol	Panax ginseng	Human colon cancer	[56]
Gossypol	Gossypium hirsutum	Colorectal cancer	[57]
Chrysin	Passiflora caerulea	Colorectal cancer	[58]
Plumbagin	Plumbago zeylanica	Liver, fibrosarcoma, leukemia, and breast cancer	[59]
6-Shogaol	Zingiber officinale	Ovary cancer	[60]
Curcumin	Curcuma longa	Breast, lung, colon, prostate esophagus, liver, and skin cancer	[61]
Ursolic acid	Oldenlandia diffusa	Lungs, ovary, uterus, stomach, liver, colon, rectum, and brain cancer	[62]
Isoliquiritigenin	Glycyrrhiza uralensis	Human lung cancer	[63]
Punarnavine	Boerrhavia diffusa	Malignant melanoma cancer	[64]
Procyanidins	Vitis vinifera	Human colon cancer	[65]
Resveratrol	Polygonum cuspidatum	Colorectal, skin, and liver cancer	[66]
Damnacanthal	Morinda citrifolia	Lung cancer, sarcomas	[67]
Gossypol	Gossypium hirsutum	Breast, stomach, liver, prostate, and bladder cancer	[68]
Niazinine A	Moringa oliefera	Blood cancer	[69]
Amooranin	Amoora rohituka	Lymphocytic leukemia	[70]
Betulinic acid	Ziziphus rugosa	Cytotoxicity against human melanoma cells	[71]
Asiatic acid	Centella asiatica	Melanoma, glioblastoma, breast cancer	[72]
Gallic acid	Leea indica	Ehrlich ascites carcinoma	[73]
Combretastatins	Combretum caffrum	Colon, leukemia, and lung cancer	[74]
Lycopene	Solanum lycopersicum	Prostate and colon cancer	[75]
Plumbagin	Plumbago zeylanica	Blood and skin cancer	[76]
Cannabinoid	Cannabis sativa	Lung, pancreas, breast, prostate, and colorectal cancer	[77]
Silymarin	Sylibum marianum	Colorectal cancer	[78]
Tylophorine	Tylophora indica	Breast cancer	[74]
Saffron	Saffron crocus	Liver, lung cancer and pancreatic cancer	[79]
nab-paclitaxel	Taxus brevifolia	Ovarian and breast cancer	[80]
Cyanidin	Vitis vinifera	Colon cancer	[81]
Actein	Actaea racemosa	Liver and breast cancer	[82]
Betulinic acid	Betula Sp.	Human melanoma xenografts and leukemia	[30]
Allin	Allium sativum	Carcinoma of human mammary gland	[83]
Neferine	Nelumbo nucifera	Liver cancer	[84]
Calcaelin	Calvatia caelata	Breast and spleen cancer cells	[85]
Lentinan	Lentinus edodes	Sarcoma-180 in mice	[86]
Schizophyllan	Schizophyllum commune	Head and neck cancer	[87]
Apigenin	Matricaria chamomilla	Colorectal cancer	[88]
Vitex	Vitex agnus-castu	Human uterine, ovarian, cervical, and breast cancer	[89]

2.2. Success Stories of Medicinal Plant-Based Anticancer Drug

Till date, more than thousand plants species have been identified with noteworthy anticancer potential [90, 91]. The isolation of the vinca alkaloids, vinblastine [92] from the Madagascar periwinkle, and Catharanthus roseus G. Don. (Apocynaceae) is one of the major examples of anticancer medication. This along with vincristine and other cancer chemotherapeutic drugs are used for the treatment of a range of cancers such as leukemias, lymphomas, advanced testicular cancer, breast and lung cancers, and Kaposi's sarcoma [30, 91]. The discovery of paclitaxel (Taxol) [93] from the bark of the Pacific Yew, Taxus brevifolia Nutt. (Taxaceae), is another major success story in natural product drug discovery. Utilization of various parts of Taxus brevifolia from which paclitaxel was discovered and other Taxus species (e.g., Taxus Canadensis Marshall and Taxus baccata L.) by several Native American Tribes kindle the idea of indigenous knowledge-based medicinal plants [30, 91]. Another potent plant-acquired active compound, Homoharringtonine [94], was extracted from the Chinese tree Cephalotaxus harringtonia var. drupacea (Sieb and Zucc.) (Cephalotaxaceae) and has been used successfully for a long time in China in a racemic mixture with harringtonine for the treatment of acute myelogenous leukemia [30]. Elliptinium, a derivative of ellipticine, isolated from a Fijian medicinal plant Bleekeria vitensis A. C. Sm., is shipped to France for the treatment of breast cancer [30, 91]. These events represent only the surface of the success story of plant-based anticancer drug discovery with a promise to find more in the near future [91].

2.3. Toddler's Step Leads to the Unknown Horizon

The question is whether long-term ignorance of natural products for drug development can fit into the multibillion-dollar pharmaceutical industry? The answer certainly depends on multiple factors. However, the bright side is that the recent advancement of multiple medicinal plant database from local and global researchers, cutting edge omics technique to accelerate to find the drug targets and unprecedented improvement on drug delivery system (Figure 1).

Figure 1.

Phytochemicals can be used as drugs based on medicinal plant database, omics study to find the target, and efficient drug delivery system.

Over the last decade, along with the effort of Moonshot^SM project, local scientists from different parts of the work tried to curate the information of traditional herbal practice, preparation, recipe, and their ailments [12, 95–97]. Furthermore, to find out the target of potential phytochemicals is easier than ever, because of advancement of genomics, proteomics, transcriptomics, and metabolomics in recent years [91, 98–100]. The final frontier of using natural products as cancer treatment depends on the efficient drug delivery system. Fortunately, the advent of nanotechnology for drug delivery system has fast-forwarded this sector over the last few years [101, 102].

3. Conclusions

If we assume the research avenue of phytochemicals as potential cancer therapeutics as an image of a pyramid, this review has demonstrated a piece of stone from that pyramid. However, the idea of pushing natural products' research on drug discovery and development requires constant update and well-documented literature. This review paper will take the reader from the ancient history of herbal medicinal practice to the modern day's isolation, purification, identification, biosynthesis, in vitro or in vivo study, drug development, efficient delivery of drugs, and therapeutic trial.

Conflicts of Interest

The author declares that there are no conflicts of interest regarding the publication of this paper.