Multani Shaleen, Saranath Dhananjaya
Department of Biological Sciences, Sunandan Divatia School of Science, NMIMS (Deemed-to-be) University, Mumbai, Maharashtra, 400056, India.
Tumour Biol. 2016 Nov;37(11):14501-14512. doi: 10.1007/s13277-016-5322-5. Epub 2016 Sep 20.
Globocan 2012 reports the global oral cancer incidence of 300,373 new oral cancer cases annually, contributing to 2.1 % of the world cancer burden. The major well-established risk factors for oral cancer include tobacco, betel/areca nut, alcohol and high-risk oncogenic human papilloma virus (HPV) 16/18. However, only 5-10 % of individuals with high-risk lifestyle develop oral cancer. Thus, genomic variants in individuals represented as single nucleotide polymorphisms (SNPs) influence susceptibility to oral cancer. With a view to understanding the role of genomic variants in oral cancer, we reviewed SNPs in case-control studies with a minimum of 100 cases and 100 controls. PubMed and HuGE navigator search engines were used to obtain data published from 1990 to 2015, which identified 67 articles investigating the role of SNPs in oral cancer. Single publications reported 93 SNPs in 55 genes, with 34 SNPs associated with a risk of oral cancer. Meta-analysis of data in multiple studies defined nine SNPs associated with a risk of oral cancer. The genes were associated with critical functions deregulated in cancers, including cell proliferation, immune function, inflammation, transcription, DNA repair and xenobiotic metabolism.
《全球癌症统计2012》报告称,全球每年有300373例新发口腔癌病例,占全球癌症负担的2.1%。已明确的口腔癌主要危险因素包括烟草、槟榔、酒精以及高危致癌性人乳头瘤病毒(HPV)16/18型。然而,只有5%至10%具有高危生活方式的个体患口腔癌。因此,以单核苷酸多态性(SNP)形式存在的个体基因组变异会影响口腔癌易感性。为了解基因组变异在口腔癌中的作用,我们回顾了病例对照研究中SNP的情况,这些研究至少有100例病例和100例对照。使用PubMed和HuGE导航器搜索引擎获取1990年至2015年发表的数据,共识别出67篇研究SNP在口腔癌中作用的文章。单篇文章报道了55个基因中的93个SNP,其中34个SNP与口腔癌风险相关。对多项研究数据进行的荟萃分析确定了9个与口腔癌风险相关的SNP。这些基因与癌症中失调的关键功能相关,包括细胞增殖、免疫功能、炎症、转录、DNA修复和外源性物质代谢。