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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2009-7-30
pubmed:abstractText
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 (32)P-postlabeling and hence a basis for susceptibility to the development of lung cancer.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1460-2180
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1368-71
pubmed:dateRevised
2011-7-15
pubmed:meshHeading
pubmed-meshheading:19465454-Adult, pubmed-meshheading:19465454-Aged, pubmed-meshheading:19465454-Aged, 80 and over, pubmed-meshheading:19465454-Carcinoma, Non-Small-Cell Lung, pubmed-meshheading:19465454-Case-Control Studies, pubmed-meshheading:19465454-Chromosomes, Human, Pair 15, pubmed-meshheading:19465454-Chromosomes, Human, Pair 5, pubmed-meshheading:19465454-Chromosomes, Human, Pair 6, pubmed-meshheading:19465454-DNA Adducts, pubmed-meshheading:19465454-Female, pubmed-meshheading:19465454-Genetic Predisposition to Disease, pubmed-meshheading:19465454-Genome-Wide Association Study, pubmed-meshheading:19465454-Genotype, pubmed-meshheading:19465454-Humans, pubmed-meshheading:19465454-Lung Neoplasms, pubmed-meshheading:19465454-Male, pubmed-meshheading:19465454-Membrane Proteins, pubmed-meshheading:19465454-Middle Aged, pubmed-meshheading:19465454-Nerve Tissue Proteins, pubmed-meshheading:19465454-Polymorphism, Single Nucleotide, pubmed-meshheading:19465454-Prognosis, pubmed-meshheading:19465454-Receptors, Nicotinic, pubmed-meshheading:19465454-Risk Factors, pubmed-meshheading:19465454-Telomerase
pubmed:year
2009
pubmed:articleTitle
The TERT-CLPTM1L lung cancer susceptibility variant associates with higher DNA adduct formation in the lung.
pubmed:affiliation
Section of Toxicology, Department of Biological and Chemical Working Environment, National Institute of Occupational Health, N-0033, Oslo, Norway. shan.zienolddiny@stami.no
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't