Abstract

BackgroundMany published data on the association between single nucleotide polymorphisms (SNPs) in the ESR1 gene and prostate cancer susceptibility are inconclusive. The aim of this Human Genome Epidemiology (HuGE) review and meta-analysis is to derive a more precise estimation of this relationship.MethodsA literature search of PubMed, Embase, Web of Science and Chinese Biomedical (CBM) databases was conducted from their inception through July 1st, 2012. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the strength of association.ResultsTwelve case-control studies were included with a total 2,165 prostate cancer cases and 3,361 healthy controls. When all the eligible studies were pooled into the meta-analysis, ESR1 PvuII (C>T) and XbaI (A>G) polymorphisms showed no association with the risk of prostate cancer. However, in the stratified analyses based on ethnicity and country, the results indicated that ESR1 PvuII (C>T) polymorphism was significantly associated with increased risk of prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may significantly increase the risk of prostate cancer among American population. Furthermore, we also performed a pooled analysis for all eligible case-control studies to explore the role of codon 10 (T>C), codon 325 (C>G), codon 594 (G>A) and +261G>C polymorphisms in prostate cancer risk. Nevertheless, no significant associations between these polymorphisms and the risk of prostate cancer were observed.ConclusionResults from the current meta-analysis indicate that ESR1 PvuII (C>T) polymorphism may be a risk factor for prostate cancer among Asian populations, especially among Indian population; while ESR1 XbaI (A>G) polymorphism may increase the risk of prostate cancer among American population.

Highlights

  • Prostate cancer is the second most frequently diagnosed cancer and the sixth leading cause of cancer deaths in males

  • Inclusion and Exclusion Criteria Studies included in our meta-analysis have to meet the following criteria: (a) case-control studies or cohort studies focused on associations between Estrogen receptor 1 (ESR1) gene polymorphisms and prostate cancer susceptibility; (b) all patients diagnosed with prostate cancer should be confirmed by pathological or histological examinations; (c) published data about the frequencies of alleles or genotypes must be sufficient; (d) studies were published in English or Chinese

  • Various genotype methods were used among these studies, including polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP), denaturing high performance liquid chromatography (DHPLC), direct DNA sequencing, Taqman, and PCR-restriction fragment length polymorphism (PCRRFLP)

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Summary

Introduction

Prostate cancer is the second most frequently diagnosed cancer and the sixth leading cause of cancer deaths in males. It accounted for 14% (903,500) of the total new cancer cases and 6% (258,400) of the total cancer deaths in males in 2008 [1]. Many published data on the association between single nucleotide polymorphisms (SNPs) in the ESR1 gene and prostate cancer susceptibility are inconclusive. The aim of this Human Genome Epidemiology (HuGE) review and metaanalysis is to derive a more precise estimation of this relationship

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