The Key Laboratory of Modern Toxicology of Ministry of Education, Department of Molecular and Genetic Toxicology, School of Public Health, Nanjing Medical University, Nanjing 210029, China.
J Cancer Res Clin Oncol. 2012 Aug;138(8):1339-45. doi: 10.1007/s00432-012-1210-6. Epub 2012 Apr 6.
Prostate stem cell antigen (PSCA) is a glycosylphosphatidylinositol-anchored 123-aa protein related to the cell-proliferation inhibition and/or cell-death induction activity. Many studies had reported the role of PSCA rs2294008 C > T and rs2976392 G > A polymorphisms on gastric cancer risk.
To investigate a more precise estimation of the relationships, we performed a meta-analysis on 9 case-control studies included 10,746 cases and 9,158 controls. Odds ratios (ORs) and 95 % confidence intervals (CIs) were used to assess the strength of the association.
For PSCA rs2294008 C > T polymorphism, there was a significantly increased risk of gastric cancer in all genetic models (TT/TC vs. CC: OR = 1.61, 95 % CI = 1.35-1.91; TT vs.
TC/CC: OR = 1.33, 95 % CI = 1.24-1.42). Similar results were also observed for PSCA rs2976392 G > A polymorphism (AA/AG vs. GG: OR = 1.69, 95 % CI = 1.24-2.31; AA vs.
AG/GG: OR = 1.36, 95 % CI = 1.24-1.50). In the stratified analysis by ethnicity of rs2294008, an increased gastric cancer risk was found in both Asians (TT vs.
TC/CC: OR = 1.31, 95 % CI = 1.22-1.42) and Europeans (TT/TC vs. CC: OR = 1.42, 95 % CI = 1.18-1.71). Furthermore, when stratified by clinicopathologic characteristics of tumor location and histology, a higher risk on non-cardia compared with cardia gastric cancer (TT vs.
TC/CC: OR = 1.43, 95 % CI = 1.12-1.83) as same as diffused compared with intestinal gastric cancer (TT vs.
TC/CC: OR = 1.29, 95 % CI = 1.13-1.49) was observed.
These findings supported that PSCA rs2294008 C > T and rs2976392 G > A polymorphisms may contribute to the susceptibility to gastric cancer, particular in non-cardia or diffused gastric cancer.
前列腺干细胞抗原(PSCA)是一种糖基磷脂酰肌醇锚定的 123 个氨基酸蛋白,与细胞增殖抑制和/或细胞死亡诱导活性有关。许多研究报道了 PSCA rs2294008 C > T 和 rs2976392 G > A 多态性与胃癌风险的关系。
为了更准确地评估这些关系,我们对 9 项病例对照研究进行了荟萃分析,共纳入 10746 例病例和 9158 例对照。使用比值比(OR)和 95%置信区间(CI)来评估关联的强度。
对于 PSCA rs2294008 C > T 多态性,所有遗传模型均显示胃癌风险增加(TT/TC 与 CC:OR = 1.61,95%CI = 1.35-1.91;TT 与 TC/CC:OR = 1.33,95%CI = 1.24-1.42)。对于 PSCA rs2976392 G > A 多态性也观察到类似的结果(AA/AG 与 GG:OR = 1.69,95%CI = 1.24-2.31;AA 与 AG/GG:OR = 1.36,95%CI = 1.24-1.50)。在按 rs2294008 的种族分层分析中,在亚洲人群(TT 与 TC/CC:OR = 1.31,95%CI = 1.22-1.42)和欧洲人群(TT/TC 与 CC:OR = 1.42,95%CI = 1.18-1.71)中均发现胃癌风险增加。此外,当按肿瘤位置和组织学的临床病理特征分层时,与贲门胃癌相比,非贲门胃癌的风险更高(TT 与 TC/CC:OR = 1.43,95%CI = 1.12-1.83),与肠型胃癌相比,弥漫型胃癌的风险更高(TT 与 TC/CC:OR = 1.29,95%CI = 1.13-1.49)。
这些发现支持 PSCA rs2294008 C > T 和 rs2976392 G > A 多态性可能导致胃癌易感性增加,特别是在非贲门或弥漫型胃癌中。