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泰国乳腺癌患者谷胱甘肽S-转移酶P1基因(GSTP1)的启动子甲基化与基因多态性

Promoter methylation and genetic polymorphism of glutathione S-transferase P1 gene (GSTP1) in Thai breast- cancer patients.

作者信息

Pongtheerat Tanett, Pakdeethai Supparit, Purisa Wichai, Chariyalertsak Sunanta, Petmitr Songsak

机构信息

Unit of Biochemistry, Department of Medical Sciences, Faculty of Science, Rangsit University, Patumthani, Thailand.

出版信息

Asian Pac J Cancer Prev. 2011;12(10):2731-4.

Abstract

The GSTP1 gene encodes for a detoxification enzyme involved in protecting cells from carcinogens. In breast cancer, GSTP1 polymorphisms may produce lower effective enzyme detoxification properties and GSTP1 promoter hypermethylation may result in inactivation of GSTP1 expression. We therefore hypothesized an influence on progression of breast cancer. To study the effect of GSTP1 polymorphisms and CpG-island hypermethylation on GSTP1 promoter, PCR-RFLP and methylation-specific PCR techniques were used with 41 Thai breast-cancer patients. Associations between the codon 105 (A to G) genetic polymorphism, CpG-island hypermethylation, and clinico-pathological parameters were analyzed. GSTP1 hypermethylation was found in 26% of cases and the GSTP1 polymorphism in 14%. GSTP1 hypermethylation was significantly associated with breast cancer; lymph-node metastasis (P = 0.02) while GSTP1 polymorphism status significantly varied with progesterone receptor positivity (P = 0.04). No association was found between the GSTP1 polymorphism and methylation status. The results indicated that CpG-island hypermethylation of the GSTP1 promoter is associated with a biologically aggressive phenotype, but may not be related to the codon 105 (A to G) gene polymorphism in breast-cancer patients.

摘要

GSTP1基因编码一种解毒酶,参与保护细胞免受致癌物侵害。在乳腺癌中,GSTP1基因多态性可能导致较低的有效酶解毒特性,而GSTP1启动子高甲基化可能导致GSTP1表达失活。因此,我们推测其对乳腺癌进展有影响。为研究GSTP1基因多态性和CpG岛高甲基化对GSTP1启动子的影响,我们对41例泰国乳腺癌患者采用了聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和甲基化特异性PCR技术。分析了密码子105(A到G)基因多态性、CpG岛高甲基化与临床病理参数之间的关联。发现26%的病例存在GSTP1高甲基化,14%存在GSTP1基因多态性。GSTP1高甲基化与乳腺癌、淋巴结转移显著相关(P = 0.02),而GSTP1基因多态性状态随孕激素受体阳性情况有显著差异(P = 0.04)。未发现GSTP1基因多态性与甲基化状态之间存在关联。结果表明,GSTP1启动子的CpG岛高甲基化与生物学侵袭性表型相关,但可能与乳腺癌患者的密码子105(A到G)基因多态性无关。

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