The Molecular Effect of Curcumin Subsidized by Radiation on HepG2 cell lines

Authors

  • A Kaed Molecular Biology, Radiation Biology Department National Centre for Radiation Research and Technology, Atomic Energy Authority, Cairo, Egypt. Author
  • A Hassan Zoology Department, Faculty of Science, Ain Shams University. Author
  • T El-Maghraby Molecular Biology, Radiation Biology Department National Centre for Radiation Research and Technology, Atomic Energy Authority, Cairo, Egypt. Author

DOI:

https://doi.org/10.48165/

Keywords:

Curcumin, Hepatocellular Carcinoma, Gamma Radiation, p53, Her2/ neu, MMP9

Abstract

Cancer is a major health problem around the world. Cancer treat ment depends on radiation therapy sometimes in combination with che motherapy or hormonal therapy. The treatment of cancer with radiation  and chemotherapy cause several unwanted harmful side effects. Turmeric  (Curcuma longa), is a type of herb widely used as a spice. Recent re searches have shown that curcumin, the active component of turmeric  possesses anticancer properties. This study aimed to evaluate the effect  of γ-radiation and curcumin each of them alone or combined on HepG2  cell line proliferation, p53, Her2/neu, and MMP9 gene expression, and total antioxidant capacity. HepG2 cells were exposed to γ-radiation (R), or treated with different concentrations of curcumin alone or combined  with each other. The cell viability was examined by MTT assay. Gene ex pression of p53, Her2/neu, and MMP9 were evaluated by using real-time  QPCR. The total antioxidant capacity (TAC) was also measured. Cur cumin or R alone or combined decreased cell viability and induced cell  death in a dose-and time-dependent manner when compared to untreated  group. Curcumin and R induced p53 gene expression, while reduced  Her2/neu, and MMP9 expression. Furthermore, the TAC was decreased  in the treated groups compared to the untreated. Conclusion: Curcumin  can sensitize HepG2 cells to radiation and would potentiate the effect of  radiotherapy in cancer..

References

• Aggarwal, B.B.; Kumar, A. and Bharti, A.C. (2003): Anticancer potential of curcumin: preclinical and clinical studies. Anticancer Res. J., (23): 363.

• Aggeli, I.K.; Koustas, E.; Gaitanaki, C. and Beis, I. (2013): Curcumin acts as a pro-oxidant inducing apoptosis via JNKs in the isolated perfused Rana ri dibunda heart. Exp. Zool. A Ecol. Genet. Physiol. J., 319(6): 328.

• Apoorv, TS.; Babu, PP.; Meese S.; Gai PP.; Be du-Addo, G. and Mockenhaupt, F.P. (2015): Ma trix metalloproteinase-9 polymorphism 1562 C > T (rs3918242) associated with protection against pla cental malaria. The Am. J., Trop. Med. Hyg. 93 (1):

• Badra, G.; Lotfy, M.; El-Refaie, A.; Obada, M.; Abdelmonem, E.; Kandeel, S. and Fathy, A. (2010): Significance of serum matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in chronic hep atitis C patients. Acta Microbiol. Immunol. Hung. J., 57(1): 29.

• Bharti, A.C.; Donato, N.; Singh, S.; and Aggar wal, B.B. (2003): Curcumin (diferuloylmethane) down-regulates the constitutive activation of nuclear factor-kappa B and IkappaBalpha kinase in human multiple myeloma cells, leading to suppression of proliferation and induction of apoptosis. Blood J., 101: 1053.

• Chan, WH.; Wu, C.C.; and Yu, J.S. (2003): Cur cumin inhibits UV irradiation-induced oxidative stress and apoptotic biochemical changes in human epidermoid carcinoma A431 cells. J., Cell Biochem., 90: 327.

• Chung, D.M.; Kim, J.H. and Kim, J.K. (2015): Evaluation of MTT and Trypan Blue assays for radi ation-induced cell viability test in HepG2 cells Int. J. Radiat. Res., 13(4): 331.

• Cuadros, M.; Talavera, P.; Lopez, F.J.; García Perez, I.; Blanco, A. and Concha, A. (2010): Real Time RT-PCR Analysis for Evaluating the Her2/neu Status in Breast Cancer. J., Pathobiology, 77:38.

• El-Naggar A.M. (2009): Medical Radiation Biology. Google Books. Medical_Radiation_Biology.html.

• El-Serag, HB. and Rudolph, KL. (2007): Hepato cellular carcinoma: epidemiology and molecular car cinogenesis. J. Gastroenterology, 132: 2557.

• Estella, C.; Herrer, I.; Atkinson, S.P.; Quinonero, A.; Martınez, S.; Pellicer A. and Simon, C. (2012): Inhibition of Histone Deacetylase Activity in Human Endometrial Stromal Cells Promotes Extracellular Matrix Remodeling and Limits Embryo Invasion. PLoS ONE J., 7(1): e30508.

• Fung, S.K. and Lok, A.S. (2005): Management of patients with hepatitis B virus-induced cirrhosis. Hepatol. J., 42: 54.

• Gallardo, M. and Calaf, G.M. (2016): Curcumin and epithelial-mesenchymal transition in breast can cer cells transformed by low doses of radiation and estrogen. Int. J. Oncol., 48(6): 2534.

• Girdhani, S.; Ahmed, M.M. and Mishra, K.P. (2009): Enhancement of Gamma Radiation-induced Cytotoxicity of Breast Cancer Cells by Curcumin. Mol. Cell. pharmacol. J., 1(4): 208.

• Khan, M.A.; Gahlot, S. and Majumdar, S. (2012): Oxidative Stress Induced by Curcumin Promotes the Death of Cutaneous T-cell Lymphoma (HuT-78) by disrupting the Function of Several Molecular Targets. Mol. Cancer Ther. J., 11:1873.

• Killeen, S.D.; Wang, J.H.; Andrews, E.J. and Red mond, H.P. (2009): Bacterial endotoxin enhances colorectal cancer cell adhesion and invasion through TLR-4 and NF-kappaB-dependent activation of the urokinase plasminogen activator system. Br. J., Can cer 100: 1589.

• Koracevic, D.; Koracevic, G.; Djordjevic, V.; An drejevic, S. and Cosic, V. (2001): Method for the measurement of antioxidant activity in human fluids. Clin. Pathol. J., 54 (5): 356.

• Koren, E.; Zverev, I.; Ginsburg, I. and Kohen, R. (2008): Supplementation with antioxidants fails to increase the total antioxidant capacity of several cell lines in culture. Biomed. Pharmacother., 62, (3):179.

• Lai, H.; Chien, S.; Kuo, S.; Tseng, l.; Lin, H., Chi, C. and Chen, D. (2012): The Potential Utility of Curcumin in the Treatment of HER-2-Overexpressed Breast Cancer: An In Vitro and In Vivo Comparison Study with Herceptin. Evid. Based Complement. Alternat. Med., 12 pages Article ID 486568. doi.

org/10.1155/2012/486568

• Li, W.; Wang, Y.; Song, Y.; Xu, L.; Zaho, J. and Fang, B. (2015): A preliminary study of the effect of curcumin on the expression of p53 protein in a human multiple myeloma cell line. Oncol. Lett., 9: 1719.

• Mitri, Z.; Constantine, T. and O’Regan, R. (2012): The HER2 Receptor in Breast Cancer: Pathophysi ology, Clinical Use, and New Advances in Therapy. Chemoth. Res. Pract. J., 743193.

• Mosmann, T. (1983): Rapid colorimetric assay for cellular growth and survival: application to prolifera tion and cytotoxicity assays. Immunol. Methods J., 16; 65(1-2):55.

• Nada, A.S. (2013): Modulating efficacy of thyme oil in rats exposed to γ-radiation. Rad. Res. J., 6(1):35.

• Rivenbark, A. and Coleman, W. (2007): The use of epigenetic biomarkers for preclinical detection of hepatocellular carcinoma: potential for noninvasive screening of high-risk populations. Clin. Cancer Res. J., 13: 2309.

• Swatson, W.S.; Katoh-Kurasawa, M.; Shaulsky, G. and Alexander, S. (2017): Curcumin affects gene expression and reactive oxygen species via a PKA dependent mechanism in Dictyostelium discoideum. PLoS ONE J., 12(11): 10.1371.

• Tan, M. and Yu, D. (2007): Molecular mechanisms of erbB2-mediated breast cancer chemoresistance. Adv. Exp. Med. Biol. J., 608: 119.

• Tong, W.; Wang, Q.; Sun, D. and Suo, J. (2016): Curcumin suppresses colon cancer cell invasion via

( 188 ) J. Nucl. Tech. Appl. Sci., Vol. 6, No. 3 Kaed A. et al.

AMPK-induced inhibition of NF-κB, uPA activator and MMP9. Oncol. Lett., 12(5): 4139.

• Vandooren, J.; Van den Steen, P.E. and Opdena kker, G. (2013): Biochemistry and molecular biology of gelatinase B or matrix metalloproteinase-9 (MMP 9) the next decade. Crit. Rev. Biochem. Mol. Biol. J., 48(3): 222.

• Veeraraghavan, J.; Natarajan, M.; Herman, T.S. and Aravindan, N. (2010): Curcumin-altered p53- Response Genes Regulate Radiosensitivity in p53- mutant Ewing’s sarcoma cells, Anticancer Res. J., 30

(10): 4007.

• Wade, M.; Wong, E.T.; Tang, M.; Stommel, J.M. and Wahl, G. (2006): Hdmx modulates the outcome of p53 activation in human tumor cells. Biol. Chem. J., 281 (44): 33036.

• Ziada, D.; El Sadany, S.; Soliman, H.; Abd-El salam, S.; Salama, M.; Hawash, N.; Selim, A.; Hamisa, M. and Elsabagh, H. (2016): Prevalence of hepatocellular carcinoma in chronic hepatitis C patients in Mid Delta, Egypt: A single center study. Egypt Nati. Canc. Inst. J., 28(4): 257.

Downloads

Published

2018-10-03

How to Cite

The Molecular Effect of Curcumin Subsidized by Radiation on HepG2 cell lines. (2018). Journal of Nuclear Technology in Applied Science, 6(3), 179–190. https://doi.org/10.48165/