Skip to main content
Top
Published in: Tumor Biology 6/2014

01-06-2014 | Research Article

Increased lung cancer risk associated with the TERT rs2736100 polymorphism: an updated meta-analysis

Authors: Jihua Yang, Shunchang Jiao

Published in: Tumor Biology | Issue 6/2014

Login to get access

Abstract

The rs2736100 polymorphism in the telomerase reverse transcriptase (TERT) gene has been implicated in lung cancer risk in multiple populations, but the existing evidence lacks statistical power to draw a convincing conclusion. Therefore, the present study was devised to derive a more precise estimation of the association between rs2736100 and lung cancer risk. The PubMed, Embase, and Web of Science databases were comprehensively searched for papers concerning lung cancer risk in relation to rs2736100. Pooled odds ratios (ORs) and the 95 % confidence intervals (CIs) were appropriately calculated using the fixed or random effects model. Meta-analysis of 20 independent studies involving 39,715 cancer cases and 61,462 control subjects showed statistical evidence for an association between rs2736100 and increased risk of lung cancer. Subgroup analysis by ethnicity demonstrated a significant association among both Asian and Caucasian populations. We additionally found an increased risk of non-small cell lung cancer and lung adenocarcinoma strongly associated with rs2736100. These data provide further evidence supporting a role for genetic susceptibility of TERT rs2736100 in the development of lung cancer.
Literature
1.
go back to reference Ferlay J et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127(12):2893–917.CrossRefPubMed Ferlay J et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127(12):2893–917.CrossRefPubMed
2.
go back to reference Chen W, Zhang S, Zou X. Evaluation on the incidence, mortality and tendency of lung cancer in China. Thoracic Cancer. 2010;1:35–40.CrossRef Chen W, Zhang S, Zou X. Evaluation on the incidence, mortality and tendency of lung cancer in China. Thoracic Cancer. 2010;1:35–40.CrossRef
3.
go back to reference Shields PG, Harris CC. Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. J Clin Oncol. 2000;18(11):2309–15.PubMed Shields PG, Harris CC. Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. J Clin Oncol. 2000;18(11):2309–15.PubMed
4.
go back to reference Kiyohara C et al. Genetic polymorphisms and lung cancer susceptibility: a review. Lung Cancer. 2002;37(3):241–56.CrossRefPubMed Kiyohara C et al. Genetic polymorphisms and lung cancer susceptibility: a review. Lung Cancer. 2002;37(3):241–56.CrossRefPubMed
5.
go back to reference Matakidou A, Eisen T, Houlston RS. Systematic review of the relationship between family history and lung cancer risk. Br J Cancer. 2005;93(7):825–33.PubMedCentralCrossRefPubMed Matakidou A, Eisen T, Houlston RS. Systematic review of the relationship between family history and lung cancer risk. Br J Cancer. 2005;93(7):825–33.PubMedCentralCrossRefPubMed
6.
go back to reference Hwang SJ et al. Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk. Hum Genet. 2003;113(3):238–43.CrossRefPubMed Hwang SJ et al. Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk. Hum Genet. 2003;113(3):238–43.CrossRefPubMed
7.
go back to reference Fletcher O et al. Lifetime risks of common cancers among retinoblastoma survivors. J Natl Cancer Inst. 2004;96(5):357–63.CrossRefPubMed Fletcher O et al. Lifetime risks of common cancers among retinoblastoma survivors. J Natl Cancer Inst. 2004;96(5):357–63.CrossRefPubMed
12.
go back to reference Miki D et al. Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. Nat Genet. 2010;42(10):893–6.CrossRefPubMed Miki D et al. Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. Nat Genet. 2010;42(10):893–6.CrossRefPubMed
13.
go back to reference Hu Z et al. A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese. Nat Genet. 2011;43(8):792–6.CrossRefPubMed Hu Z et al. A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese. Nat Genet. 2011;43(8):792–6.CrossRefPubMed
14.
go back to reference Jin G et al. Common genetic variants on 5p15.33 contribute to risk of lung adenocarcinoma in a Chinese population. Carcinogenesis. 2009;30(6):987–90.CrossRefPubMed Jin G et al. Common genetic variants on 5p15.33 contribute to risk of lung adenocarcinoma in a Chinese population. Carcinogenesis. 2009;30(6):987–90.CrossRefPubMed
15.
go back to reference Kohno T et al. Contribution of the TP53, OGG1, CHRNA3, and HLA-DQA1 genes to the risk for lung squamous cell carcinoma. J Thorac Oncol. 2011;6(4):813–7.CrossRefPubMed Kohno T et al. Contribution of the TP53, OGG1, CHRNA3, and HLA-DQA1 genes to the risk for lung squamous cell carcinoma. J Thorac Oncol. 2011;6(4):813–7.CrossRefPubMed
16.
go back to reference Wang Y et al. Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers. Carcinogenesis. 2010;31(2):234–8.CrossRefPubMed Wang Y et al. Role of 5p15.33 (TERT-CLPTM1L), 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) variation and lung cancer risk in never-smokers. Carcinogenesis. 2010;31(2):234–8.CrossRefPubMed
17.
go back to reference Shiraishi K et al. A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. Nat Genet. 2012;44(8):900–3.CrossRefPubMed Shiraishi K et al. A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. Nat Genet. 2012;44(8):900–3.CrossRefPubMed
18.
go back to reference Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58.CrossRefPubMed Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58.CrossRefPubMed
19.
go back to reference Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst. 1959;22(4):719–48.PubMed Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst. 1959;22(4):719–48.PubMed
20.
22.
go back to reference Zhong R, et al. Genetic variations in TERT-CLPTM1L locus are associated with risk of lung cancer in Chinese population. Mol Carcinog, 2013;52 Suppl 1:E118–26. Zhong R, et al. Genetic variations in TERT-CLPTM1L locus are associated with risk of lung cancer in Chinese population. Mol Carcinog, 2013;52 Suppl 1:E118–26.
23.
24.
go back to reference Zhao Z et al. Significant association of 5p15.33 (TERT-CLPTM1L genes) with lung cancer in Chinese Han population. Exp Lung Res. 2013;39(2):91–8.CrossRefPubMed Zhao Z et al. Significant association of 5p15.33 (TERT-CLPTM1L genes) with lung cancer in Chinese Han population. Exp Lung Res. 2013;39(2):91–8.CrossRefPubMed
25.
go back to reference Brenner DR et al. Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Hum Genet. 2013;132(5):579–89.PubMedCentralCrossRefPubMed Brenner DR et al. Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Hum Genet. 2013;132(5):579–89.PubMedCentralCrossRefPubMed
26.
go back to reference Bae EY et al. Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population. Respirology. 2012;17(4):699–706.CrossRefPubMed Bae EY et al. Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population. Respirology. 2012;17(4):699–706.CrossRefPubMed
27.
go back to reference Chen XF et al. Multiple variants of TERT and CLPTM1L constitute risk factors for lung adenocarcinoma. Genet Mol Res. 2012;11(1):370–8.CrossRefPubMed Chen XF et al. Multiple variants of TERT and CLPTM1L constitute risk factors for lung adenocarcinoma. Genet Mol Res. 2012;11(1):370–8.CrossRefPubMed
28.
go back to reference Yoon KA et al. A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. Hum Mol Genet. 2010;19(24):4948–54.CrossRefPubMed Yoon KA et al. A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. Hum Mol Genet. 2010;19(24):4948–54.CrossRefPubMed
29.
go back to reference Myneni AA et al. Genetic polymorphisms of TERT and CLPTM1L and risk of lung cancer—a case-control study in a Chinese population. Lung Cancer. 2013;80(2):131–7.PubMedCentralCrossRefPubMed Myneni AA et al. Genetic polymorphisms of TERT and CLPTM1L and risk of lung cancer—a case-control study in a Chinese population. Lung Cancer. 2013;80(2):131–7.PubMedCentralCrossRefPubMed
30.
go back to reference Ito H et al. Association between a genome-wide association study-identified locus and the risk of lung cancer in Japanese population. J Thorac Oncol. 2012;7(5):790–8.CrossRefPubMed Ito H et al. Association between a genome-wide association study-identified locus and the risk of lung cancer in Japanese population. J Thorac Oncol. 2012;7(5):790–8.CrossRefPubMed
31.
go back to reference Lan Q et al. Longer telomere length in peripheral white blood cells is associated with risk of lung cancer and the rs2736100 (CLPTM1L-TERT) polymorphism in a prospective cohort study among women in China. PLoS One. 2013;8(3):e59230.PubMedCentralCrossRefPubMed Lan Q et al. Longer telomere length in peripheral white blood cells is associated with risk of lung cancer and the rs2736100 (CLPTM1L-TERT) polymorphism in a prospective cohort study among women in China. PLoS One. 2013;8(3):e59230.PubMedCentralCrossRefPubMed
32.
go back to reference Lan Q et al. Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia. Nat Genet. 2012;44(12):1330–5.PubMedCentralCrossRefPubMed Lan Q et al. Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia. Nat Genet. 2012;44(12):1330–5.PubMedCentralCrossRefPubMed
33.
go back to reference Truong T et al. Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the international lung cancer consortium. J Natl Cancer Inst. 2010;102:959–71.PubMedCentralCrossRefPubMed Truong T et al. Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the international lung cancer consortium. J Natl Cancer Inst. 2010;102:959–71.PubMedCentralCrossRefPubMed
36.
go back to reference Shen M et al. A prospective study of telomere length measured by monochrome multiplex quantitative PCR and risk of lung cancer. Lung Cancer. 2011;73(2):133–7.PubMedCentralCrossRefPubMed Shen M et al. A prospective study of telomere length measured by monochrome multiplex quantitative PCR and risk of lung cancer. Lung Cancer. 2011;73(2):133–7.PubMedCentralCrossRefPubMed
37.
go back to reference Fu X et al. Relative telomere length: a novel non-invasive biomarker for the risk of non-cirrhotic hepatocellular carcinoma in patients with chronic hepatitis B infection. Eur J Cancer. 2012;48(7):1014–22.PubMedCentralCrossRefPubMed Fu X et al. Relative telomere length: a novel non-invasive biomarker for the risk of non-cirrhotic hepatocellular carcinoma in patients with chronic hepatitis B infection. Eur J Cancer. 2012;48(7):1014–22.PubMedCentralCrossRefPubMed
38.
39.
go back to reference Shen J et al. Genetic polymorphisms in telomere pathway genes, telomere length, and breast cancer survival. Breast Cancer Res Treat. 2012;134(1):393–400.PubMedCentralCrossRefPubMed Shen J et al. Genetic polymorphisms in telomere pathway genes, telomere length, and breast cancer survival. Breast Cancer Res Treat. 2012;134(1):393–400.PubMedCentralCrossRefPubMed
40.
go back to reference Cong YS, Wen J, Bacchetti S. The human telomerase catalytic subunit hTERT: organization of the gene and characterization of the promoter. Hum Mol Genet. 1999;8(1):137–42.CrossRefPubMed Cong YS, Wen J, Bacchetti S. The human telomerase catalytic subunit hTERT: organization of the gene and characterization of the promoter. Hum Mol Genet. 1999;8(1):137–42.CrossRefPubMed
41.
go back to reference Li C et al. Genetic variants in TERT-CLPTM1L genetic region associated with several types of cancer: a meta-analysis. Gene. 2013;526(2):390–9.CrossRefPubMed Li C et al. Genetic variants in TERT-CLPTM1L genetic region associated with several types of cancer: a meta-analysis. Gene. 2013;526(2):390–9.CrossRefPubMed
42.
go back to reference Wang HM, Zhang XY, Jin B. TERT genetic polymorphism rs2736100 was associated with lung cancer: a meta-analysis based on 14,492 subjects. Genet Test Mol Biomarkers. 2013;17(12):937–41.PubMedCentralCrossRefPubMed Wang HM, Zhang XY, Jin B. TERT genetic polymorphism rs2736100 was associated with lung cancer: a meta-analysis based on 14,492 subjects. Genet Test Mol Biomarkers. 2013;17(12):937–41.PubMedCentralCrossRefPubMed
Metadata
Title
Increased lung cancer risk associated with the TERT rs2736100 polymorphism: an updated meta-analysis
Authors
Jihua Yang
Shunchang Jiao
Publication date
01-06-2014
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 6/2014
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-014-1765-8

Other articles of this Issue 6/2014

Tumor Biology 6/2014 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine