Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer

Questa Hope1, Sarah Bullock, Christopher Evans

  • 1Translational Cancer Genetics Team, Section of Cancer Genetics and Urology Unit, Male Urological Centre and Institute of Cancer Research and Royal Marsden NHS Trust, Surrey, United Kingdom.

Abstract

Insights

This study found no evidence that the MSR1 999C>T mutation increases prostate cancer risk. Further analysis suggests this variant is unlikely to confer more than a two-fold risk.

Area of Science:

  • Genetics
  • Oncology
  • Molecular Biology

Background:

  • Genetic variants in the macrophage scavenger receptor 1 (MSR1) gene have been linked to prostate cancer.
  • Previous small studies suggested the MSR1 999C>T (R293X) mutation may elevate prostate cancer risk.

Purpose of the Study:

  • To investigate the association between the MSR1 999C>T mutation and prostate cancer risk.
  • To validate findings from smaller studies using a large-scale, multi-country analysis.

Main Methods:

  • Analysis of MSR1 999C>T mutation in 2,943 prostate cancer cases and 2,870 male controls across Western countries.
  • Utilized case-control, cohort, and family studies, employing unconditional logistic regression and segregation analysis.
  • Conducted a meta-analysis combining study data with previously published research.

Main Results:

  • The prevalence of the MSR1 999C>T mutation did not differ significantly between cases (0.027) and controls (0.022).
  • Adjusted risk ratios for prostate cancer associated with the mutation were 1.31 (P=0.16) from logistic regression and 1.20 (P=0.16) from segregation analysis.
  • Meta-analysis yielded a risk ratio of 1.34 (P=0.10), indicating no significant association.

Conclusions:

  • Large-scale analysis provides no evidence supporting an increased risk of prostate cancer due to the MSR1 999C>T mutation.
  • Meta-analysis indicates it is improbable that this mutation confers a greater than two-fold increased risk for prostate cancer.