The P275A Polymorphism in the Macrophage Scavenger Receptor 1 Gene and Prostate Cancer Risk: a Meta-Analysis

Qiao-Xia Zhou1, Jian-Qiu Tang, Fen Zhao

  • 1West China School of Preclinical and Forensic Medicine, Sichuan University, Sichuan Province, China

Abstract

Insights

This meta-analysis found no significant association between the MSR1 P275A polymorphism and prostate cancer risk. The macrophage scavenger receptor 1 (MSR1) P275A variant is unlikely to be a contributing factor for developing prostate cancer.

Area of Science:

  • Genetics
  • Oncology
  • Molecular Biology

Background:

  • Inconclusive evidence links the macrophage scavenger receptor 1 (MSR1) P275A polymorphism to prostate cancer (PCa) risk.
  • Previous studies show conflicting results regarding the MSR1 P275A polymorphism's role in PCa development.

Purpose of the Study:

  • To comprehensively evaluate the genetic risk associated with the MSR1 P275A polymorphism in prostate cancer.
  • To clarify the association between the MSR1 P275A polymorphism and prostate cancer susceptibility through a meta-analysis.

Main Methods:

  • A systematic literature search was conducted across multiple databases (PubMed, Medline, Embase, etc.) up to April 27, 2015.
  • Meta-analysis included 12 case-control studies comprising 5,017 cases and 4,869 controls.
  • Statistical analyses were performed using Revman 5.2 and STATA 10.1 software.

Main Results:

  • No significant association was found between the MSR1 P275A polymorphism and PCa risk across various genetic models (dominant, co-dominant, recessive, over-dominant, allelic).
  • Stratified analyses by ethnicity (white, yellow, black, mixed) and study design (population-based, hospital-based) also revealed no significant associations.
  • Pooled analysis of 5,017 cases and 4,869 controls did not support a link between the MSR1 P275A polymorphism and prostate cancer.

Conclusions:

  • The P275A polymorphism in the macrophage scavenger receptor 1 (MSR1) gene is unlikely to be a risk factor for prostate cancer.
  • This comprehensive meta-analysis suggests that the MSR1 P275A variant does not contribute significantly to prostate cancer development.

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