A V141L polymorphism of the human LRMP gene is associated with survival of lung cancer patients
Author(s) -
Giacomo Manenti,
Federica Galbiati,
Angela Pettinicchio,
Monica Spinola,
Silvia Piconese,
Vera P. Leoni,
Bárbara Conti,
Fernando Ravagnani,
Matteo Incarbone,
Ugo Pastorino,
Tommaso A. Dragani
Publication year - 2006
Publication title -
carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.688
H-Index - 204
eISSN - 1460-2180
pISSN - 0143-3334
DOI - 10.1093/carcin/bgi332
Subject(s) - lung cancer , single nucleotide polymorphism , medicine , lung cancer susceptibility , adenocarcinoma , oncology , proportional hazards model , biology , lung , locus (genetics) , gene , genetics , genotype , cancer
Mouse Lrmp and Casc1 genes are candidates for the pulmonary adenoma susceptibility 1 (Pas1) locus, the major determinant of strain variation in lung tumor susceptibility. These genes contain coding and non-coding single nucleotide polymorphisms (SNPs) strongly associated with lung tumor risk in mice. Analysis of LRMP and CASC1 gene SNPs in 361 lung adenocarcinoma (ADCA) patients and 327 healthy controls revealed common SNPs in LRMP (V141L and S197C) and CASC1 (R33S and three intronic variations), and none showed a significant association with lung ADCA risk. However, in the time-dependent Cox regression model, after adjustment for age, gender, smoking history and clinical stage, the carrier status of the Leu variation (V141L) of the LRMP gene was associated with higher mortality in patients with age at tumor onset < or = 65 years [hazard ratio (HR) 2.3; 95% CI 1.4-3.7; P = 0.001]. These findings suggest that the LRMP V141L polymorphism can predict survival in lung ADCA and that the role of LRMP and CASC1 in human lung cancer risk may differ from that in mice.
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