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Association between telomere length and mitochondrial copy number and cancer risk in humans: A meta-analysis on more than 300,000 individuals.
Giaccherini, Matteo; Gentiluomo, Manuel; Fornili, Marco; Lucenteforte, Ersilia; Baglietto, Laura; Campa, Daniele.
Affiliation
  • Giaccherini M; Department of Biology, University of Pisa, 56126, Pisa, Italy. Electronic address: matteo.giaccherini@phd.unipi.it.
  • Gentiluomo M; Department of Biology, University of Pisa, 56126, Pisa, Italy. Electronic address: manuel.gentiluomo@biologia.unipi.it.
  • Fornili M; Department of Clinical and Experimental Medicine, University of Pisa, 56126, Pisa, Italy. Electronic address: marco.fornili@med.unipi.it.
  • Lucenteforte E; Department of Clinical and Experimental Medicine, University of Pisa, 56126, Pisa, Italy. Electronic address: ersilia.lucenteforte@unipi.it.
  • Baglietto L; Department of Clinical and Experimental Medicine, University of Pisa, 56126, Pisa, Italy. Electronic address: laura.baglietto@unipi.it.
  • Campa D; Department of Biology, University of Pisa, 56126, Pisa, Italy. Electronic address: daniele.campa@unipi.it.
Crit Rev Oncol Hematol ; 167: 103510, 2021 Nov.
Article in En | MEDLINE | ID: mdl-34695574
ABSTRACT
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Telomere / Neoplasms Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Crit Rev Oncol Hematol Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Telomere / Neoplasms Type of study: Clinical_trials / Etiology_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Crit Rev Oncol Hematol Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2021 Document type: Article
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