Department of Oncology, Taizhou People's Hospital, Taizhou, 225300, Jiangsu, China.
Department of Urology, The Affiliated Changzhou No.2 People's Hospital of Nanjing Medical University, 29 Xinglong Alley, Changzhou, 213003, Jiangsu Province, China.
Sci Rep. 2020 Aug 7;10(1):13384. doi: 10.1038/s41598-020-70223-7.
Previous studies have investigated the association of the rs1805087 A/G variant of Methionine synthase gene with the susceptibility to prostate cancer (PCa). Nevertheless, the conclusions remain divergent. We performed a systemic analysis with odds ratios (ORs) and 95% confidence intervals (95% CIs) to assess Methionine synthase rs1805087 A/G variant and PCa risk. Furthermore, we utilized in silico analysis to investigate the relationship between Methionine synthase expression and the overall survival (OS) time. Totally, 10,666 PCa patients and 40,750 controls were included. We observed that Methionine synthase rs1805087 A/G variant is associated with an elevated risk of PCa (G-allele vs. A-allele: OR = 1.06, 95% CI = 1.01-1.11, P = 0.013; heterozygous model: OR = 1.08, 95% CI = 1.02-1.14, P = 0.009; dominant model: OR = 1.08, 95% CI = 1.02-1.14, P = 0.007). During stratified analysis, similar results were obtained in Asian populations, hospital-based, high quality studies and that with large sample size. Moreover, in silico analysis indicated the Methionine synthase expression is down-regulated in both young and old PCa subjects (P < 0.05). Compared with the normal subjects, the down-regulated expression of Methionine synthase was found in PCa cases with Gleason score 6 to 9. Our study showed that Methionine synthase rs1805087 A/G variant may be associated with susceptibility of PCa, especially in Asian populations, hospital-based studies and that with high quality and large sample size. Furthermore, Methionine synthase rs1805087 A/G variant may be related to the prognosis of PCa.
先前的研究已经探讨了甲硫氨酸合成酶基因 rs1805087A/G 变体与前列腺癌 (PCa) 易感性的关联。然而,结论仍然存在分歧。我们使用比值比 (OR) 和 95%置信区间 (95%CI) 进行了系统分析,以评估甲硫氨酸合成酶 rs1805087A/G 变体与 PCa 风险之间的关系。此外,我们还利用计算机分析来研究甲硫氨酸合成酶表达与总生存期 (OS) 之间的关系。总共纳入了 10666 名 PCa 患者和 40750 名对照。我们发现甲硫氨酸合成酶 rs1805087A/G 变体与 PCa 风险增加相关 (G 等位基因与 A 等位基因相比:OR=1.06,95%CI=1.01-1.11,P=0.013;杂合子模型:OR=1.08,95%CI=1.02-1.14,P=0.009;显性模型:OR=1.08,95%CI=1.02-1.14,P=0.007)。在分层分析中,在亚洲人群、基于医院的高质量研究和大样本量研究中也得到了类似的结果。此外,计算机分析表明,在年轻和老年 PCa 患者中,甲硫氨酸合成酶的表达均下调 (P<0.05)。与正常对照相比,在 Gleason 评分 6 至 9 的 PCa 病例中发现甲硫氨酸合成酶的下调表达。本研究表明,甲硫氨酸合成酶 rs1805087A/G 变体可能与 PCa 的易感性相关,特别是在亚洲人群、基于医院的研究和高质量、大样本量的研究中。此外,甲硫氨酸合成酶 rs1805087A/G 变体可能与 PCa 的预后相关。