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Prognostic potential of the MDM2 309T>G polymorphism in stage I lung adenocarcinoma.

Authors :
Enokida Y
Shimizu K
Atsumi J
Kakegawa S
Takase Y
Kaira K
Yashima H
Araki T
Nakazawa S
Ohtaki Y
Nagashima T
Alexander L
Usui K
Ishikawa T
Hayashizaki Y
Takeyoshi I
Source :
Cancer medicine [Cancer Med] 2016 Aug; Vol. 5 (8), pp. 1791-801. Date of Electronic Publication: 2016 May 26.
Publication Year :
2016

Abstract

The MDM2 protein plays an important role in the regulation of cell proliferation and apoptosis via ubiquitination and proteasome-mediated degradation of p53. The genetic polymorphism rs2279744 (c.309T>G) of the MDM2 gene is reportedly associated with susceptibility and/or prognosis in various cancers. In this study, we investigated the risk factors for worse survival in patients with lung adenocarcinoma (AC). We examined the association between c.309T>G and the prognosis of lung cancer by retrospectively reviewing 453 lung cancer patients. We studied both, clinicopathological and genetic characteristics, including the c.309T>G, p53 Arg72Pro, EGFR, KRAS, and p53 mutations. Associations between these factors and survival outcome were analyzed using Cox proportional hazards models. The frequencies of MDM2 polymorphisms were T/T, 20.8%; T/G, 48.6%, and G/G, 30.7%. The overall survival (OS) of AC patients with pathological stage I disease and the MDM2 T/T genotype was significantly shorter than that of those with the T/G or G/G genotypes (P = 0.02). Multivariate analysis revealed that the MDM2 T/T genotype was an independent, significant prognostic factor (hazard ratio [HR] = 2.23; 95% confidence interval [CI]: 1.07-4.65; P = 0.03). The MDM2 T/T genotype was predictive of poorer survival in a Japanese population. Genotyping for this polymorphism might predict the clinical outcomes of stage I AC patients.<br /> (© 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
2045-7634
Volume :
5
Issue :
8
Database :
MEDLINE
Journal :
Cancer medicine
Publication Type :
Academic Journal
Accession number :
27228500
Full Text :
https://doi.org/10.1002/cam4.750