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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
Background:
Published data regarding associations between the P275A polymorphism in the macrophage scavenger receptor 1 (MSR1) gene and prostate cancer (PCa) risk are inconclusive. The aim of this study was to comprehensively evaluate the genetic risk of P275A polymorphism in MSR1 gene for PCa.
Materials And Methods:
A systematic literature search was carried out in Pubmed, Medline (Ovid), Embase, CBM, CNKI, Weipu, and Wanfang databases, covering all available publications (last search was performed on Apr 27, 2015). Statistical analysis was performed using Revman 5.2 and STATA 10.1 software.
Results:
A total of 5,017 cases and 4,869 controls in 12 case-control studies were included in this meta-analysis. When all groups were pooled, there was no evidence that the P275A polymorphism had a significant association with PCa under dominant (OR=0.93, 95%CI=0.81-1.06, and p=0.28), co-dominant (homogeneous OR=0.97, 95%CI=0.56-1.68, and p=0.92; heterogeneous OR=0.93, 95%CI=0.74-1.15, and p=0.49), recessive (OR=1.10, 95%CI=0.65-1.87, and p=0.73), over-dominant (OR=0.93, 95%CI=0.75-1.15, and p=0.50), and allelic (OR=0.95, 95%CI=0.77-1.16, and p=0.61) genetic models. For stratified analyses by ethnicity and study design, no significant associations were found in the white race, the yellow race, the black race and mixed ethnicity, and the population-based case-control (PCC) and hospital-based case-control (HCC) studies under all genetic models.
Conclusions:
Based on our meta-analysis, the P275A polymorphism in the MSR1 gene is unlikely to be a risk factor for PCa.
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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