TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.

BACKGROUND: Some common genetic variants of TERT-CLPTM1L gene, which encode key protein subunits of telomerase, have been suggested to play a crucial role in tumorigenesis. The TERT-CLPTM1L polymorphism rs401681 was of special interest for cancers risk but with inconclusive results. METHODOLOGY/PRIN...

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Main Authors: Jieyun Yin, Yangkai Li, Ming Yin, Jingwen Sun, Li Liu, Qin Qin, Xiaorong Li, Lu Long, Shaofa Nie, Sheng Wei
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3511286?pdf=render
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spelling doaj-557b15f00f1040e3a31cc64b31f76e2d2020-11-25T02:39:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e5065010.1371/journal.pone.0050650TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.Jieyun YinYangkai LiMing YinJingwen SunLi LiuQin QinXiaorong LiLu LongShaofa NieSheng WeiBACKGROUND: Some common genetic variants of TERT-CLPTM1L gene, which encode key protein subunits of telomerase, have been suggested to play a crucial role in tumorigenesis. The TERT-CLPTM1L polymorphism rs401681 was of special interest for cancers risk but with inconclusive results. METHODOLOGY/PRINCIPAL FINDINGS: We performed a comprehensive meta-analysis of 29 publications with a total of 91263 cases and 735952 controls. We assessed the strength of the association between rs401681 and overall cancers risk and performed subgroup analyses by cancer type, ethnicity, source of control, sample size and expected power. Rs401681 C allele was found to be associated with marginally increased cancers risk, with per allele OR of 1.04 (95%CI = 1.00-1.08, P(heterogeneity)<0.001) and an expected power of 1.000. Following further stratified analyses, the increased cancers risk were discovered in subgroups of lung, bladder, prostate, basal cell carcinomas and Asians, while a declined risk of pancreatic cancer and melanoma were detected. CONCLUSIONS/SIGNIFICANCE: These findings suggested that rs401681 C allele was a low-penetrance risk allele for the development of cancers of lung, bladder, prostate and basal cell carcinoma, but a potential protective allele for melanoma and pancreatic cancer.http://europepmc.org/articles/PMC3511286?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jieyun Yin
Yangkai Li
Ming Yin
Jingwen Sun
Li Liu
Qin Qin
Xiaorong Li
Lu Long
Shaofa Nie
Sheng Wei
spellingShingle Jieyun Yin
Yangkai Li
Ming Yin
Jingwen Sun
Li Liu
Qin Qin
Xiaorong Li
Lu Long
Shaofa Nie
Sheng Wei
TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
PLoS ONE
author_facet Jieyun Yin
Yangkai Li
Ming Yin
Jingwen Sun
Li Liu
Qin Qin
Xiaorong Li
Lu Long
Shaofa Nie
Sheng Wei
author_sort Jieyun Yin
title TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
title_short TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
title_full TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
title_fullStr TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
title_full_unstemmed TERT-CLPTM1L polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
title_sort tert-clptm1l polymorphism rs401681 contributes to cancers risk: evidence from a meta-analysis based on 29 publications.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description BACKGROUND: Some common genetic variants of TERT-CLPTM1L gene, which encode key protein subunits of telomerase, have been suggested to play a crucial role in tumorigenesis. The TERT-CLPTM1L polymorphism rs401681 was of special interest for cancers risk but with inconclusive results. METHODOLOGY/PRINCIPAL FINDINGS: We performed a comprehensive meta-analysis of 29 publications with a total of 91263 cases and 735952 controls. We assessed the strength of the association between rs401681 and overall cancers risk and performed subgroup analyses by cancer type, ethnicity, source of control, sample size and expected power. Rs401681 C allele was found to be associated with marginally increased cancers risk, with per allele OR of 1.04 (95%CI = 1.00-1.08, P(heterogeneity)<0.001) and an expected power of 1.000. Following further stratified analyses, the increased cancers risk were discovered in subgroups of lung, bladder, prostate, basal cell carcinomas and Asians, while a declined risk of pancreatic cancer and melanoma were detected. CONCLUSIONS/SIGNIFICANCE: These findings suggested that rs401681 C allele was a low-penetrance risk allele for the development of cancers of lung, bladder, prostate and basal cell carcinoma, but a potential protective allele for melanoma and pancreatic cancer.
url http://europepmc.org/articles/PMC3511286?pdf=render
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