Polymorphisms of Survivin and Its Protein Expression Are Associated with Colorectal Cancer Susceptibility in Chinese Population

被引:21
|
作者
Li, Xia-Bin [1 ]
Li, Shi-Ning [1 ]
Yang, Zhi-Hui [1 ]
Cao, Ling [2 ]
Duan, Fang-Lei [1 ]
Sun, Xing-Wang [1 ]
机构
[1] Luzhou Med Coll, Dept Pathol, Luzhou 646000, Sichuan, Peoples R China
[2] Luzhou Med Coll, Affiliated Hosp 1, Dept Nephrol, Luzhou 646000, Sichuan, Peoples R China
关键词
SQUAMOUS-CELL CARCINOMA; LUNG-CANCER; GENE; PROMOTER; APOPTOSIS; PROLIFERATION; CONTRIBUTE; MECHANISM; DIVISION; NUCLEAR;
D O I
10.1089/dna.2012.1912
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
To investigate the association of survivin -31G/C, -141G/C, and -241T/C polymorphisms with colorectal cancer (CRC) susceptibility and explore the mechanisms of the survivin polymorphism in CRC development. A case-control study was conducted of 275 CRC cases and 270 healthy controls. Polymorphisms of survivin -31G/C, -141G/C, and -241T/C were genotyped by polymerase chain reaction-restriction fragment length polymorphism. Survivin and Ki-67 expression was analyzed by immunohistochemistry by the Envision technique for the paraffin sections of 152 CRC. It showed that the -31G/C genotype and allele distribution were significantly different between the CRC cases and controls. The -31CC genotype and -31C allele were over-represented among the CRC cases. Compared with the CC genotype, the GC and GG genotypes had a significantly decreased risk of CRC (p = 0.015). Survivin and Ki-67 expression of patients with the CC genotype was significantly higher than the patients with the GC and GG genotypes. In addition, a significantly positive correlation was found between expression of Survivin and Ki-67. There were no significant difference of the -141G/C and -241T/C polymorphism distributions among cases and controls. Survivin 31G/C may adjust the Survivin expression, and it might contribute to a risk of developing CRC.
引用
收藏
页码:236 / 242
页数:7
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