2'-5' oligoadenylate synthetase 1 polymorphism is associated with prostate cancer
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Updated: Jun 1, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Sanjay Mandal1, Fisseha Abebe, Jaideep Chaudhary
1Center For Cancer Research and Therapeutics Development, Clark Atlanta University, Atlanta, Georgia 30314, USA.
Background:
The antiviral, proapoptotic, antiproliferative gene 2'-5' oligoadenylate synthetase (2-5OAS1) converts adenosine triphosphate into a series of 2'-5' oligoadenylates (2-5A). In turn, 2-5A activates latent ribonuclease (RNaseL), a candidate hereditary prostate cancer gene. OAS1 polymorphism (reference single nucleotide polymorphism [SNP] 2660 [rs2660]) has been associated with increased susceptibility to infections and various diseases. In general, the low-enzyme-activity adenine-adenine (AA) genotype promotes susceptibility, whereas the high-enzyme-activity guanosine-guanosine (GG) genotype confers protection. In this study, the authors investigated the association of this functional OAS1 polymorphism (rs2660) with prostate cancer.
Methods:
Sample size and power were calculated using a power calculation software program for case-control genetic association analyses. Genomic DNA samples from a control group (n = 140) and from a case group of patients with prostate cancer (n = 164) were used for genotyping SNPs rs2660, rs1131454, and rs34137742 in all samples. Statistical analyses were performed using a logistic regression model.
Results:
A significant association was observed between the rs2660 genotype (A/G) and prostate cancer. Genotype AA increased the risk, whereas genotype GG decreased the risk of prostate cancer. The GG genotype was not observed in the African American samples. The AA genotype also increased the risk of prostate cancer with age.
Conclusions:
The OAS1 SNP rs2660 AA genotype was associated significantly with prostate cancer, whereas the GG genotype protected against prostate cancer. OAS1 rs2660 may be a prostate cancer susceptibility polymorphism, which is a significant observation, especially in a context of the OAS1-RNaseL pathway. Thus, a functional defect in OAS1 because of the rs2660 SNP not only can attenuate RNaseL function but also can alter cell growth and apoptosis independent of RNaseL.
Insights
The OAS1 rs2660 AA genotype significantly increases prostate cancer risk, while the GG genotype offers protection. This OAS1 polymorphism may influence cancer development and progression.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- The 2'-5' oligoadenylate synthetase (2-5OAS1) gene plays a role in antiviral and antiproliferative pathways.
- A specific polymorphism in OAS1 (rs2660) affects enzyme activity and has been linked to disease susceptibility.
- The adenine-adenine (AA) genotype is generally associated with lower enzyme activity and increased susceptibility, while the guanosine-guanosine (GG) genotype is linked to higher activity and protection.
Purpose of the Study:
- To investigate the association between the functional OAS1 polymorphism (rs2660) and prostate cancer risk.
- To determine if specific genotypes of OAS1 rs2660 influence susceptibility or protection against prostate cancer.
Main Methods:
- Case-control genetic association study.
- Genotyping of OAS1 SNPs rs2660, rs1131454, and rs34137742 in 164 prostate cancer cases and 140 controls.
- Statistical analysis using logistic regression.
Main Results:
- A significant association was found between the OAS1 rs2660 genotype and prostate cancer.
- The AA genotype was linked to an increased risk of prostate cancer, particularly with age.
- The GG genotype was associated with a decreased risk of prostate cancer; this genotype was not observed in African American samples.
Conclusions:
- The OAS1 rs2660 polymorphism, specifically the AA genotype, is significantly associated with increased prostate cancer risk.
- The GG genotype appears to be protective against prostate cancer.
- This functional OAS1 SNP may impact prostate cancer development by affecting OAS1-RNaseL pathway function and cellular processes like growth and apoptosis.
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