Skip Navigation


Carcinogenesis Advance Access originally published online on May 22, 2009
Carcinogenesis 2009 30(8):1368-1371; doi:10.1093/carcin/bgp131
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
30/8/1368    most recent
bgp131v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Zienolddiny, S.
Right arrow Articles by Haugen, A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zienolddiny, S.
Right arrow Articles by Haugen, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

The TERT-CLPTM1L lung cancer susceptibility variant associates with higher DNA adduct formation in the lung

Shanbeh Zienolddiny*, Vidar Skaug, Nina E. Landvik, David Ryberg, David H. Phillips1, Richard Houlston2 and Aage Haugen

Section of Toxicology, Department of Biological and Chemical Working Environment, National Institute of Occupational Health, N-0033, Oslo, Norway
1 Section of Molecular Carcinogenesis
2 Section of Cancer Genetics, Institute of Cancer Research, Cotswold Road, Surrey SM2 5NG, UK

* To whom correspondence should be addressed. Tel: +47 23195284; Fax: +47 23195203; Email: shan.zienolddiny{at}stami.no

Genome-wide association studies have provided evidence that common variation at 5p15.33 [telomerase reverse transcriptase (TERT)-cleft lip and palate transmembrane 1-like (CLPTM1L)], 6p21.33 and 15q25.1 (CHRNA5-CHRNA3) influences lung cancer risk and cancer types with strong environmental risk factors. To independently validate these associations, we compared 5p15.33 (rs402710, rs401681), 6p21.33 (rs4324798) and 15q25.1 (rs1051730, rs16969968 and rs8034191) genotypes in 365 non-small cell lung cancer cases and 440 controls. Consistent with published data, variant genotypes of 5p15 (rs402710), 6p21 and 15q25 showed dose-dependent associations with lung cancer risk. To examine if variants influence the impact of environmental risk factors on lung carcinogenesis, we studied the relationship between genotype and levels of bulky aromatic/hydrophobic DNA adducts in lung tissue adjacent to tumor from 204 lung cancer cases. The risk allele of rs402710 (TERT-CLPTM1L locus) was associated with significantly higher levels of bulky aromatic/hydrophobic DNA adducts (P = 0.02). These data demonstrate a potential association between the TERT-CLPTM1L variant and levels of bulky DNA adducts measured by 32P-postlabeling and hence a basis for susceptibility to the development of lung cancer.

Abbreviations: CLPTM1L, cleft lip and palate transmembrane 1-like; NNK, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone; SNP, single-nucleotide polymorphism; TERT, telomerase reverse transcriptase

Received April 2, 2009; revised May 13, 2009; accepted May 19, 2009.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.