Cargando…
Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis
Accumulating epidemiological evidence indicates that the quantitative changes in human mitochondrial DNA (mtDNA) copy number could affect the genetic susceptibility of malignancies in a tumor-specific manner, but the results are still elusive. To provide a more precise estimation on the association...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075889/ https://www.ncbi.nlm.nih.gov/pubmed/27775013 http://dx.doi.org/10.1038/srep35859 |
_version_ | 1782461941841657856 |
---|---|
author | Hu, Liwen Yao, Xinyue Shen, Yi |
author_facet | Hu, Liwen Yao, Xinyue Shen, Yi |
author_sort | Hu, Liwen |
collection | PubMed |
description | Accumulating epidemiological evidence indicates that the quantitative changes in human mitochondrial DNA (mtDNA) copy number could affect the genetic susceptibility of malignancies in a tumor-specific manner, but the results are still elusive. To provide a more precise estimation on the association between mtDNA copy number and risk of diverse malignancies, a meta-analysis was conducted by calculating the pooled odds ratios (OR) and the 95% confidence intervals (95% CI). A total of 36 case-control studies involving 11,847 cases and 15,438 controls were finally included in the meta-analysis. Overall analysis of all studies suggested no significant association between mtDNA content and cancer risk (OR = 1.044, 95% CI = 0.866–1.260, P = 0.651). Subgroup analyses by cancer types showed an obvious positive association between mtDNA content and lymphoma and breast cancer (OR = 1.645, 95% CI = 1.117–2.421, P = 0.012; OR = 1.721, 95% CI = 1.130–2.622, P = 0.011, respectively), and a negative association for hepatic carcinoma. Stratified analyses by other confounding factors also found increased cancer risk in people with drinking addiction. Further analysis using studies of quartiles found that populations with the highest mtDNA content may be under more obvious risk of melanoma and that Western populations were more susceptible than Asians. |
format | Online Article Text |
id | pubmed-5075889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50758892016-10-28 Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis Hu, Liwen Yao, Xinyue Shen, Yi Sci Rep Article Accumulating epidemiological evidence indicates that the quantitative changes in human mitochondrial DNA (mtDNA) copy number could affect the genetic susceptibility of malignancies in a tumor-specific manner, but the results are still elusive. To provide a more precise estimation on the association between mtDNA copy number and risk of diverse malignancies, a meta-analysis was conducted by calculating the pooled odds ratios (OR) and the 95% confidence intervals (95% CI). A total of 36 case-control studies involving 11,847 cases and 15,438 controls were finally included in the meta-analysis. Overall analysis of all studies suggested no significant association between mtDNA content and cancer risk (OR = 1.044, 95% CI = 0.866–1.260, P = 0.651). Subgroup analyses by cancer types showed an obvious positive association between mtDNA content and lymphoma and breast cancer (OR = 1.645, 95% CI = 1.117–2.421, P = 0.012; OR = 1.721, 95% CI = 1.130–2.622, P = 0.011, respectively), and a negative association for hepatic carcinoma. Stratified analyses by other confounding factors also found increased cancer risk in people with drinking addiction. Further analysis using studies of quartiles found that populations with the highest mtDNA content may be under more obvious risk of melanoma and that Western populations were more susceptible than Asians. Nature Publishing Group 2016-10-24 /pmc/articles/PMC5075889/ /pubmed/27775013 http://dx.doi.org/10.1038/srep35859 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hu, Liwen Yao, Xinyue Shen, Yi Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title | Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title_full | Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title_fullStr | Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title_full_unstemmed | Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title_short | Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis |
title_sort | altered mitochondrial dna copy number contributes to human cancer risk: evidence from an updated meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075889/ https://www.ncbi.nlm.nih.gov/pubmed/27775013 http://dx.doi.org/10.1038/srep35859 |
work_keys_str_mv | AT huliwen alteredmitochondrialdnacopynumbercontributestohumancancerriskevidencefromanupdatedmetaanalysis AT yaoxinyue alteredmitochondrialdnacopynumbercontributestohumancancerriskevidencefromanupdatedmetaanalysis AT shenyi alteredmitochondrialdnacopynumbercontributestohumancancerriskevidencefromanupdatedmetaanalysis |