Chemopreventive Efficacy of Ginger Extract (Zingiber officinale)
Abstract
The liver cells were cultured in the presence of ginger extract at various concentrations (0-1 mg /ml) for 24 h and the cells viability and proliferation rate were evaluated by MTS and BrdU assays, while apoptosis was evaluated by colorimetric determination of caspase 8 and 3 activities. Ginger extract exhibited a dose dependent inhibition of viability and proliferation of WRL-68, HLE and HepG2 cells with IC50 of 569.69 ± 7.99 µg/ml, 389.71 ± 26.56 µg/ml and 358.71 ± 17.12 µg/ml respectively. Ginger extract induced apoptosis through activation of caspase-8 and 3 in a dose dependent pattern for all cells at concentration ranging from 0-500 mg/ml. We found that antiproliferative effect of ginger extract could be associated with induction of apoptosis as shown by increased activities of caspase 8 and 3.The results from this study suggest that ginger extract has chemopreventive properties against hepatoma cells HepG2 and HLE by inhibiting cellular proliferation and inducing apoptosis.
Keywords : antiproliferation, apoptosis, caspases, Zingiber officinale
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Feo, F., De Miglio, M. R., Simile, M. M., Muroni, M.R., Calvisi, D.F., Frau, M. and Pascale, R.M. 2006. Hepatocellular carcinoma as a complex polygenic disease. Interpretative analysis of recent development on genetic predisposition. Biochim. Biophys. Acta 1765: 126-147..
Thorgeirsson, S.S. and Grisham, J.W. 2002. Molecular pathogenesis of human hepatocellular carcinoma. Nature Gen. 31: 339- 346.
Wild, C.P. and Hall, A.J. 2000. Primary prevention of hepatocellular carcinoma in developing countries. Mutation Res. 462: 381-393.
Wang, X.W., Hussain, S.P., Huo, T.I., Wu, C.G., Forgues, M., Hofseth, L.J., Brechot, C. and Harris, C.C. 2002. Molecular pathogenesis of human hepatocellular carcinoma. Toxicology 181-182: 43-47.
Farinati, F., Cardin, R., Fiorentino, M., D’Errico, A., Grigioni, W. and Cecchetto, A. 2001. Imbalance between cytoproliferation and apoptosis in hepatitis C virus related chronic liver disease. J. Viral Hepatitis 8: 34-40.
Issa, A.Y., Volate, S.R. and Wargovich, M.J. 2006. The role of phytochemicals in inhibition of cancer and inflammation: New directions and perspectives. J. Food Comp. Anal. 19: 405-419.
Gosslau, A. and Chen, K.Y. 2004. Nutraceuticals, apoptosis and disease prevention. Nutrition 20: 95-102.
Tjendraputra, E., Tran, V.H., Brennan, D.L., Roufogalis, B.D. and Duke, C.C. 2001. Effect of ginger constituents and synthetic analogues on cyclooxygenase-2 enzyme in intact cells. Bioorganic Chem. 29: 156-163.
Chrubasik, S., Pittler, M.H. and Roufogalis, B.D. 2005. Zingiberis rhizome: a comprehensive review on the ginger effect and efficacy profiles. Phytomedicine 12: 684-701.
Bhattacharjee, S.K. 2000. Ginger (Zingiber officinale). In Handbook of aromatic plants, 473-474. India: Pointer Publishers.
Mascolo, N., Jain, R., Jain, S.C. and Capasso, F. 1989. Ethnopharmacologic investigation of ginger (Zingiber officinale). J. Ethnopharmacol. 27(1-2): 129-140.
Lee, E. and Surh, Y-J. 1998. Induction of apoptosis in HL-60 cells by pungent vanilloids [6]- gingerol and [6]-paradol. Cancer Lett. 134: 163-168.
Surh, Y-J., Lee, E. and Lee, J-M. 1998. Chemoprotective properties of some pungent ingredients present in red pepper and ginger. Mutation Res. 402: 259-267.
Sujatha, R. and Srinivas, L. 1995. Modulation of lipid peroxidation by dietary components. Toxicol. In Vitro 9(3): 231-236.
Lee, E., Park, K-K., Lee, J-M., Chun, K-S., Kang, J-Y., Lee, S-S. and Surh, Y-J. 1998. Suppression of mouse skin tumor promotion and induction of apoptosis in HL-60 cells by Alpinia oxyphylla Miquel (Zingiberaceae). Carcinogenesis 19(8): 1377-1381.
Lee, J-Y., Hwang, W-I. and Lim, S-T. 2004. Antioxidant and anticancer activities of organic extracts from Platycodon grandiflorum A. De Candolle roots. J. Ethnopharmacol. 93: 409-415.
Keum, Y-S., Kim, J., Lee, K.H., Park, K.K., Surh, Y-J., Lee, J.M., Lee, S-S., Yoon, J.H., Joo, S.Y., Cha, I.H. and Yook, J.I. 2002. Induction of apoptosis and caspase-3 activation by chemopreventive [6]-paradol and structurally related compounds in KB cells. Cancer Lett. 177: 41-47.
Tong, X., Lin, S., Fujii, M. and Hou, D-X. 2004. Molecular mechanisms of echinocystic acid-induced apoptosis in HepG2 cells.Biochem.Biophys. Res.Comm., 321: 539-546.
Hsu, Y-L., Kuo, P-L. and Lin, C-C. 2004. Acacetin inhibits the proliferation of HepG2 by blocking cell cycle progression and inducing apoptosis. Biochem. Pharmacol. 67: 823-829.
Bold, R.J., Termuhlen, P. M. and McConkey, D.J. 1997. Apoptosis, cancer and cancer theraphy. Surgical Oncol. 6: 133-142.
Budihardjo, I., Oliver, H., Lutter, M., Luo, X. and Wang, X. 1999. Biochemical pathways of caspase activation during apoptosis. Annu. Rev. Cell Dev. Biol. 15: 269-290.
DOI: http://dx.doi.org/10.14499/indonesianjcanchemoprev1iss2pp118-123
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