Timóteo Mafalda, Tavares Ana, Cruz Sara, Campos Carla, Medeiros Rui, Sousa Hugo
Molecular Oncology and Viral Pathology Group (CI-IPOP), Portuguese Oncology Institute of Porto, 4200-072 Porto, Portugal.
Pathology Department, Portuguese Oncology Institute of Porto, 4200-072 Porto, Portugal.
Biomed Rep. 2021 Aug;15(2):69. doi: 10.3892/br.2021.1445. Epub 2021 Jun 17.
Gastric cancer (GC) is the 5th most common type of cancer, with the 3rd highest mortality rate worldwide in both sexes. Murine double minute 2 (MDM2) protein is the major negative regulator of p53, and genetic polymorphisms in this gene have shown to be associated with several types of cancer. In the present study, a literature search was performed using PubMed and Scopus with the following key word combinations 'gastric cancer AND polymorphism AND MDM2'. Studies were carefully revised according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to identify eligible studies that matched the inclusion criteria. Statistical analysis was performed to assess the association between the different genetic polymorphisms and GC risk, by calculating the odds ratios (OR) and the confidence intervals (CI), with a 5% level of significance. A total of 11 manuscripts studied MDM2 polymorphisms in GC: rs937283 (n=1), rs3730485 (n=1) and rs2279744 (n=9). Both the rs937283 and rs3730485 reports showed an association with GC; however, there was only one study on each of these polymorphisms in the literature. A meta-analysis was performed for the rs2279744 polymorphism, of which studies showed a positive association between the G allele and risk of GC, either in the dominant model (OR=1.46; 95% CI 1.21-1.75; P<0.001) or recessive model (OR 1.65; 95% CI 1.45-1.87; P<0.001). In conclusion, genetic polymorphisms in MDM2 seemed to be associated with an increased risk of GC development, nevertheless, the number of studies were relatively low and the studied populations were primarily Chinese. The present meta-analysis emphasizes the need for additional studies in other populations to corroborate the association of these polymorphisms with GC.
胃癌(GC)是全球第5大常见癌症类型,在全球范围内男女死亡率均位居第3。小鼠双微体2(MDM2)蛋白是p53的主要负调节因子,该基因的遗传多态性已显示与多种癌症类型相关。在本研究中,使用PubMed和Scopus进行文献检索,关键词组合为“胃癌 AND 多态性 AND MDM2”。根据系统评价和Meta分析的首选报告项目指南对研究进行仔细修订,以确定符合纳入标准的合格研究。通过计算比值比(OR)和置信区间(CI),进行统计分析以评估不同基因多态性与GC风险之间的关联,显著性水平为5%。共有11篇手稿研究了GC中的MDM2多态性:rs937283(n = 1)、rs3730485(n = 1)和rs2279744(n = 9)。rs937283和rs3730485的报告均显示与GC相关;然而,文献中关于这些多态性的研究均仅有一项。对rs2279744多态性进行了Meta分析,研究表明,在显性模型(OR = 1.46;95% CI 1.21 - 1.75;P < 0.001)或隐性模型(OR 1.65;95% CI 1.45 - 1.87;P < 0.001)中,G等位基因与GC风险之间存在正相关。总之,MDM2基因多态性似乎与GC发生风险增加相关,然而,研究数量相对较少,且研究人群主要为中国人。本Meta分析强调需要在其他人群中进行更多研究,以证实这些多态性与GC的关联。