Related Experiment Video
Updated: Aug 19, 2026

MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR (qPCR)
Published on: May 16, 2012
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.
Background:
Variants in the gene encoding the macrophage scavenger receptor 1 (MSR1(4)) protein have been identified in men with prostate cancer, and several small studies have suggested that the 999C>T (R293X) protein-truncating mutation may be associated with an increased risk for this disease.
Methods:
Using large case-control, cohort, and prostate cancer family studies conducted in several Western countries, we tested for the 999C>T mutation in 2,943 men with invasive prostate carcinoma, including 401 males from multiple-case families, 1,982 cases unselected for age, and 575 men diagnosed before the age of 56 years, and in 2,870 male controls. Risk ratios were estimated by unconditional logistic regression adjusting for country and by a modified segregation analysis. A meta-analysis was conducted pooling our data with published data.
Results:
The prevalence of MSR1*999C>T mutation carriers was 0.027 (SE, 0.003) in cases and 0.022 (SE, 0.002) in controls, and did not differ by country, ethnicity, or source. The adjusted risk ratio for prostate cancer associated with being a 999C>T carrier was 1.31 [95% confidence interval (CI), 0.93-1.84; P = 0.16]. The modified segregation analysis estimated the risk ratio to be 1.20 (95% CI, 0.87-1.66; P = 0.16). The risk ratio estimated from the meta-analysis was 1.34 (95% CI, 0.94-1.89; P = 0.10).
Conclusion:
Our large-scale analysis of case and controls from several countries found no evidence that the 999C>T mutation is associated with increased risk of prostate cancer. The meta-analysis suggests it is unlikely that this mutation confers more than a 2-fold increased risk.
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.
Related Concept Videos
The Ras Gene
Ras is a superfamily...
Abnormal Proliferation
