端粒
癌症
荟萃分析
孟德尔随机化
线粒体DNA
肿瘤科
内科学
生物信息学
生物
遗传学
医学
基因型
基因
遗传变异
作者
Matteo Giaccherini,Manuel Gentiluomo,Marco Fornili,Ersilia Lucenteforte,Laura Baglietto,Daniele Campa
标识
DOI:10.1016/j.critrevonc.2021.103510
摘要
In the last decades the association of leukocyte telomere length (LTL) and mitochondrial copy number (mtDNAcn) with cancer risk has been the focus of many reports, however the relation is not yet completely understood. A meta-analysis of 112 studies including 64,184 cancer cases and 278,641 controls that analysed LTL and mtDNAcn in relation to cancer risk has been conducted to further our understanding of the topic. Stratified analyses for tumor type were also performed. Overall, no association was observed for all cancer combined neither for LTL nor mtDNAcn. Significant associations were detected for these biomarkers and specific cancer type; however, a large degree of heterogeneity was present, even within the same tumor type. Alternatives approaches based on polymorphic variants, such as polygenic risk scores and mendelian randomization, could be adopted to unravel the causal correlation of telomere length and mitochondrial copy number with cancer risk.
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