Sheehan Brock J, Edwards Bryson, Medrano Ivanna Soto, El-Saidi Mohammed A, Zaidan Wissam R, El-Ezzi Asmahan A, Kuddus Ruhul H
Department of Biology, Utah Valley University, Orem, UT 84058, USA.
Department of Strategic Management and Operations, Utah Valley University, Orem, UT 84058, USA.
Oncotarget. 2025 Apr 4;16:262-272. doi: 10.18632/oncotarget.28710.
The polymorphic genes PTGS1 and PTGS2 encode cyclooxygenases COX-1 and COX-2, respectively. Overexpression of these cyclooxygenases is linked to inflammation and neoplasms. This study investigated the potential association between the single nucleotide polymorphism (SNP) -842A>G (rs10306114) of the PTGS1 gene and SNP-765G>C (rs20417) of the PTGS2 gene with prostate cancer (PCa) and benign prostate hyperplasia (BPH). Blood leucocyte DNA from 56 healthy individuals, 61 individuals with PCa, and 51 individuals with BPH were genotyped using the PCR-RFLP method. Associations were inferred by calculating odds ratios (OR) and relative risks (RR) of genotype distributions and allele frequencies. The genotypes for both SNPs were in Hardy-Weinberg equilibrium for all groups. No significant association was observed between the A or G alleles or the AA, AG, or GG genotypes of the SNP-842A>G of the PTGS1 gene and prostatic diseases. However, the C allele of SNP-765G>C of the PTGS2 gene was significantly associated with an increased risk of BPH (OR = 2.30, -value = 0.01). Differences in the ratios of GG/GC and GG/(GC+CC) genotypes also suggested a potential association between the C allele and PCa (-value <0.1), and the combined affected (PCa+BPH) group (-value <0.04). The small sample size and sampling from one ethnic group are limitations of this study.
多态性基因PTGS1和PTGS2分别编码环氧化酶COX - 1和COX - 2。这些环氧化酶的过表达与炎症和肿瘤有关。本研究调查了PTGS1基因的单核苷酸多态性(SNP)-842A>G(rs10306114)和PTGS2基因的SNP - 765G>C(rs20417)与前列腺癌(PCa)和良性前列腺增生(BPH)之间的潜在关联。使用PCR - RFLP方法对56名健康个体、61名PCa患者和51名BPH患者的血液白细胞DNA进行基因分型。通过计算基因型分布和等位基因频率的优势比(OR)和相对风险(RR)来推断关联。所有组中两个SNP的基因型均处于哈迪 - 温伯格平衡。未观察到PTGS1基因的SNP - 842A>G的A或G等位基因或AA、AG或GG基因型与前列腺疾病之间存在显著关联。然而,PTGS2基因的SNP - 765G>C的C等位基因与BPH风险增加显著相关(OR = 2.30,P值 = 0.01)。GG/GC和GG/(GC + CC)基因型比例的差异也表明C等位基因与PCa(P值 <0.1)以及合并受累(PCa + BPH)组(P值 <0.04)之间存在潜在关联。本研究的局限性在于样本量小且来自单一民族。