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p53与印度女性子宫内膜异位症风险

p53 and risk of endometriosis in Indian women.

作者信息

Govatati Suresh, Chakravarty Baidyanath, Deenadayal Mamata, Kodati Vijaya Lakshmi, Manolla Madhavi Latha, Sisinthy Shivaji, Bhanoori Manjula

机构信息

Department of Biochemistry, Osmania University, Hyderabad, India.

出版信息

Genet Test Mol Biomarkers. 2012 Aug;16(8):865-73. doi: 10.1089/gtmb.2011.0295. Epub 2012 Jul 11.

DOI:10.1089/gtmb.2011.0295
PMID:22784258
Abstract

AIM

To investigate the role of loss of heterozygosity (LOH), single nucleotide polymorphisms (SNPs), and the expression of gene p53 in the pathogenesis of endometriosis.

METHODS

LOH at the p53 gene locus (17p13.1) was examined in matched ectopic and eutopic endometrial tissues from 31 endometriosis patients by polymerase chain reaction (PCR)-GeneScan analysis. The genotyping of selected p53 SNPs (n=10) was carried out on genomic DNA of blood from endometriosis patients (n=720) and controls (n=500) by PCR sequencing. The p53 expression levels were analyzed in the endometrial tissues from endometriosis patients (n=5) and controls (n=4) by Western blot and immunohistochemical analysis.

RESULTS

LOH was observed at the 17p13.1 locus (38.7%) in the ectopic endometrium but not in the eutopic endometrium of patients. The genotype (p=0.909) and allele (p=0.729) distribution of the p53 codon Arg72Pro polymorphism was not significantly different between patients and controls. The polymorphism was not observed at codon 47 along the other SNPs studied. There was no preferential loss of either "Arg72" or "Pro72" alleles among the LOH-positive heterozygous cases. In addition, decreased p53 expression was observed more often in the endometrium of patients than in controls.

CONCLUSIONS

p53 SNPs are not associated with endometriosis in Indian women. However, LOH and reduced expression of p53 are related with the risk of endometriosis in Indian women.

摘要

目的

探讨杂合性缺失(LOH)、单核苷酸多态性(SNP)以及p53基因表达在子宫内膜异位症发病机制中的作用。

方法

采用聚合酶链反应(PCR)-基因扫描分析,检测31例子宫内膜异位症患者配对的异位和在位子宫内膜组织中p53基因位点(17p13.1)的杂合性缺失情况。通过PCR测序,对720例子宫内膜异位症患者和500例对照者血液中的基因组DNA进行10个选定p53 SNP的基因分型。采用蛋白质免疫印迹法和免疫组织化学分析法,分析5例子宫内膜异位症患者和4例对照者子宫内膜组织中p53的表达水平。

结果

患者异位子宫内膜17p13.1位点存在杂合性缺失(38.7%),而在位子宫内膜未出现。患者与对照者之间p53密码子Arg72Pro多态性的基因型(p = 0.909)和等位基因(p = 0.729)分布无显著差异。在所研究的其他SNP中,密码子47未观察到多态性。在杂合性缺失阳性的杂合病例中,未观察到“Arg72”或“Pro72”等位基因的优先缺失。此外,与对照者相比,患者子宫内膜中p53表达降低更为常见。

结论

在印度女性中,p53 SNP与子宫内膜异位症无关。然而,p53杂合性缺失和表达降低与印度女性子宫内膜异位症风险相关。

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