Table 1.
Overview of the cytotoxic activities of Ferula species
Plant Name |
Important
Compound |
Biological activity | cell line |
Tested concentrations
(IC 50 ) µg/mL |
Mechanism of action | Reference |
---|---|---|---|---|---|---|
F.vesceritensis | Lapiferin | Cytotoxic Apoptotic |
MCF7 MCF7 |
12.85 10 |
Anticancer activity Induction of apoptotic cell death through enhancement of DNA fragmentation, activation of caspases and induction of histone acetylation |
Gamal-Eldeen and Hegazy, 2010 |
F. assa-foetida | 8-acetoxy-5-hydroxy Umbelliprenin |
Cytotoxic | A549 | 15.09 | Potent and specific inhibition of NF-κB | Appendino et al., 2006 |
F. assa-foetida | Coumarin compounds | Cytotoxic | HepG2 | Inhibition of mutagenesis, DNA destruction andcancer cells proliferation while increasing proteolyticenzymes activity | Asadisamani et al., 2015 | |
F. gummosa | Sesquiterpenes, coumarins | Cytotoxic | HepG2 | Induction of cell cycle arrest and apoptosis | Asadisamani et al., 2015 | |
F. assa-foetida | Ferutinin | Cytotoxic | CT26 HT29 | 26 29 |
Induction of apoptosis | Arghiani et al., 2014 |
F. communis | Ferulenol | Cytotoxic | MCF-7 | 1 | Reorganization of the microtubule network in MCF-7 cells and alteration of nuclear morphology | Altmann and Gertsch, 2006 |
F. sinkiangensis | Ethyl acetate Fraction |
Cytotoxic | MCF7 | 9.0 mg/L | Inhibition of tumor cell proliferation | Zhang et al., 2015a |
F. lutea | Methyl caffeate | Cytotoxic | HCT-116 IGROV-1 OVCAR-3 |
22.5±2.4 17.8±1.1 25±1.1 |
Not-mentioned | Znati et al., 2014a |
F.szowitziana | Dendrosomal farnesiferol C |
Antiproliferative and Apoptotic | AGS (gastric cancer) | >150 μΜ (24h) 80 μΜ (48h) |
Significant time- and dose-dependent suppression of AGS cells proliferation | Aas et al., 2015 |
F. assa-foetida | kellerin | Antiviral | HSV-1 | concentrations of 10, 5 and 2.5 μg/mL |
Reduction of viral titre of the HSV-1 DNA viral strains KOS | Ghannadi et al., 2014 |
F. pseudalliacea | Kamolonol, 4′-hydroxy kamolonol acetate,and farnesiferon B | Cytotoxic | HeLa-60 | 3.8, 4.5, and 7.7μM, respectively |
Seemingly, these compounds interfere with fundamental processes of growth and metabolism of the cells. | Dastan et al., 2014a |
F. lutea | n-butanol extract | Cytotoxic | K562 | 40 μg/mL | Low cytotoxicity compared to doxorubicin. | Znati et al., 2014b |
F. szowitsiana | Auraptene | Cytotoxic | MCF7 | 59.7 μM | Induction of a sub-G1 peak in the flow cytometry histogram, DNA fragmentation and apoptosis as well as up-regulation of Bax expression. | Mousavi et al., 2015 |
F. szowitsiana | Chimganin-Chimgin | Cytotoxic | MCF-7 | 45.2 for Chimginand 28 for Chimganin |
Not-mentioned. | Sahranavard et al., 2009 |
F. sinkiangensis | DAW22 | Apoptotic | C6 glioma cell | 18.92 μM in 24h | Induction of apoptosis through ER stress and mitochondrial death-receptor mediated pathways. | Zhang et al., 2015b |
F. gummosa | Ethanolic extract | Cytotoxic | BHY (human oral squamous | (0.001±1.2 mg/mL) in 72h | Induction of apoptosis and cell-cycle arrestin G1/S phase. | Gudarzi et al., 2014 |
F. szowitsiana | Umbelliprenin | Antigenotoxic | human lymphocytes | 25 to 400 μM | Inhibition of H2O2-induced DNA damage. | Soltani et al., 2009 |
F. ovina | Ferutinin | Apoptotic | MCF7, TCC and HFF3 | 29, 24 and 36 μg/ml, respectively | Induction of apoptosis. | Matin et al., 2014 |
F. szowitsiana | Farnesiferol C | Antitumor | Human umbilical vein endothelial cells (HUVEC) | 1 mg/kg body weight | Inhibition of VEGFR1. | Lee et al., 2010 |
F. badrakema | Mogoltacin | Increasing the Cytotoxicity of vincristine | TCC | Inhibition of P-glycoprotein-mediateddrug transport | BehnamRassouli et al., 2009 | |
F. pseudalliacea | Sanandajin | Cytotoxic | HeLa cells | 2.2 µM | Not mentioned. | Dastan et al., 2014b |
F. ovina | Tschimgine | Acetylcholinesterase inhibitory effect | Red blood cell (RBC) AchE | (inhibition 63.5%) | Anti-cholinesterase activity | Karimi et al., 2010 |
F. narthex | Sesquiterpenecoumarins | Anticancer | PC3 cells | 14.074±0.414μg/mL | Not mentioned. | Alam et al., 2016 |
F. oopoda | Dehydrooopodin | Cytotoxic | MCF7 and K562 | 15 and 5µM, respectively | Not mentioned. | Kasaian et al., 2014a |
F. assa-
foetida |
Methanolic extract | Cytotoxic | MDA-MB-231 Cell Line | About 650 μg/mL In 72h |
Not mentioned. | Vahabi et al., 2014 |
F. gummsa | Ethanolic extract | Cytotoxic | Gastric cancer, AGS |
37.47 µg/mL | Induction of apoptosis via induction of DNA fragmentation and plasma membrane translocation of phosphatidyl serine. | Gharaei et al., 2013 |
F. szowitsiana | Umbelliprenin | Apoptotic | Jurkat T-CLL | Induction of caspase-mediated apoptosis. Activation of intrinsic and extrinsic pathways of apoptosis by activation of caspase-9 and caspase-8. | Gholami et al., 2013 | |
F. szowitsiana | Umbelliprenin | Cytotoxic | QUDB and A549 lung cancer |
47±5.3 μM and 52±1.97 μM, respectively | Induction of apoptosis. | Khaghanzadeh et al., 2012 |