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Curcumin induced apoptosis is mediated through oxidative stress in mutated p53 and wild type p53 colon adenocarcinoma cell lines
被引:22
|作者:
Sritharan, Sruthi
[1
]
Sivalingam, Nageswaran
[1
]
机构:
[1] SRM Inst Sci & Technol, Dept Biotechnol, Sch Bioengn, Kattankulathur 603203, Tamil Nadu, India
关键词:
colorectal cancer;
curcumin;
p53;
reactive oxygen species;
CYCLE ARREST;
ROS;
CYTOTOXICITY;
ACTIVATION;
GROWTH;
D O I:
10.1002/jbt.22616
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Curcumin has anti-oxidant, anti-cancer and anti-carcinogen property. Our laboratory had previously reported that, curcumin treatment induces reactive oxygen species (ROS) generation in HT-29 cell line, an effect contradictory to its anti-oxidant property. This study evaluates the role of p53 in curcumin mediated ROS generation and cell death. Curcumin induced ROS was determined by 2',7'-dichlorofluorescein and apoptosis by Hoechst33342/PI staining in HT-29 and HCT-116 cell lines. ROS generation occurs within 1 hour of 40 mu M curcumin treatment and a reduction was observed by third hour in HCT-116 insinuating p53 involvement. N-acetyl cysteine (NAC) pre-treatment effectively quenched ROS and inhibited membrane potential loss in HT-29, but less effective in HCT-116. Mitochondrial membrane potential loss is evident with 10 and 40 mu M curcumin in HCT-116 and at 40 mu M curcumin in HT-29. Total p53 protein level increase was observed by 24 hours in HCT-116 upon NAC pre-treatment. Our results indicate that curcumin induces ROS mediated cell death in colon adenocarcinoma cell lines and may be mediated via p53.
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