Effect of curcumin and resveratrol on the cell cycle regulation, apoptosis and inhibition of metastasis related proteins in HN-4 cells.
- Author:
Sa Yub KIM
1
;
Sang Han LEE
;
Taeg Kyu KWON
Author Information
1. Dept. of Oral and Maxillofacial Surgery, School of Dentistry, Kyungpook National University, Korea. shalee@knu.ac.kr
- Publication Type:Original Article
- Keywords:
Curcumin;
Resveratrol;
Cancer chemopreventive agent
- MeSH:
Apoptosis*;
Caspase 3;
Cell Cycle Proteins;
Cell Cycle*;
Cell Death;
Complementary Therapies;
Curcuma;
Curcumin*;
Cytochromes c;
Cytosol;
Down-Regulation;
Gelatin;
Neoplasm Metastasis*;
Plants;
Plants, Medicinal;
Reactive Oxygen Species;
Rhizome;
Vitis
- From:Journal of the Korean Association of Oral and Maxillofacial Surgeons
2003;29(5):272-281
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Nontraditional or alternative medicine is becoming an increasingly attractive approach for the treatment of various inflammatory disorders and cancers. Curcumin is the major constitute of turmoric powder extracted from the rhizomes of the plant Curcuma longa. Resveratrol is a phytoalexin present in grapes and a variety of medicinal plants. In this report, We investigated the effect of curcumin and resveratrol on regulatory protein of cell cycle, induction of apoptosis and MMP activity. Treatment with 75 M curcumin for 24 hrs produced morphological changing in HN-4 cells. Curcumin and resveratrol inhibited the cellular growth in HN-4 cells. Inhibition of cell growth was associated with down-regulation of cell cycle regulatory proteins. Curcumin-induced caspase-3 activation and Bax degradation were dose-dependent with a maximal effect at a concentration of 100 M. The elevated caspase-3 activity in curcumin treated HN-4 cells are correlated with down-regulation of survivin and cIAP1, but not cIAP2. Curcumin induced a dose-dependent increase of cytochrome c in the cytosol. Curcumin induced-apoptosis was mediated through the release of cytochrome c. In addition, curcumin-induced apoptosis was caused by the generation of reactive oxygen species, which was prevented by antioxidant N-acetyl-cysteine (NAC). Cotreatment with NAC markedly prevented cytochrome c release, Bax cleavage and cell death. Also resveratrol-induced apoptosis was preceded by down-regulation of the anti-apoptotic Bcl-2, cIAP1, and caspase-3 activity. However, resveratrol-induced apoptosis was not prevented by antioxidant NAC. In addition, HN-4 cells release basal levels of MMP2 when cultured in serum-free medium. Treatment of the cells with various concentrations of PMA for 24 hr induced the expression and secretion of latent MMP9 as determined by gelatin zymography. HN-4 cells were treated with various concentrations of curcumin and resveratrol in the presence of 75 nM PMA, and MMP2 and 9 activities were inhibited by curcumin and resveratrol. These findings have implications for developing curcumin-based anticancer and anti-inflammation therapies.
