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TP53 codon 72 polymorphism and colorectal cancer susceptibility: a meta-analysis
被引:25
|作者:
Wang, Jing-Jun
[1
]
Zheng, Yuan
[1
]
Sun, Liang
[2
]
Wang, Li
[1
]
Yu, Peng-Bo
[1
]
Dong, Jian-Hua
[1
]
Zhang, Lei
[1
]
Xu, Jing
[1
]
Shi, Wei
[1
]
Ren, Yu-Chun
[1
]
机构:
[1] Dept Ctr Dis Control & Prevent Shaanxi Prov, Xian 710043, Shaanxi, Peoples R China
[2] Dept Ctr Dis Control & Prevent Fuyang, Fuyang, Peoples R China
关键词:
TP53;
Codon;
72;
Colorectal cancer;
Meta-analysis;
AGE-OF-ONSET;
P53;
CODON-72;
INCREASED RISK;
LUNG-CANCER;
ARG72PRO POLYMORPHISMS;
CAUCASIAN POPULATION;
COLON-CANCER;
GENE;
ASSOCIATION;
ADENOCARCINOMAS;
D O I:
10.1007/s11033-010-0619-8
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:
Colorectal cancer constitutes a significant proportion of the global burden of cancer morbidity and mortality. A number of studies have been conducted to explore whether TP53 codon 72 polymorphism is associated with colorectal cancer susceptibility. However, controversial results were obtained. In order to derive a more precise estimation of the relationship, we systematically searched Medline, Google scholar, and Ovid database for studies reported before May 2010. A total of 3603 colorectal cancer cases and 5524 controls were included. TP53 codon 72 polymorphism was not associated with colorectal cancer risk in all genetic models (for dominant model: OR = 0.99, 95% CI: 0.86-1.15; for recessive model: OR = 1.00, 95% CI: 0.81-1.23; for Arg/Pro vs. Arg/Arg: OR = 1.00, 95% CI: 0.87-1.15; for Pro/Pro vs. Arg/Arg: OR = 0.97, 95% CI: 0.76-1.25). In the subgroup analyses by ethnic groups and sources of controls, no significant associations were found in all models. Taken together, this meta-analysis suggested that the biologically usefulness of TP53 codon 72 polymorphism as a selection marker in colorectal cancer susceptibility may be very limited.
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页码:4847 / 4853
页数:7
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