A common polymorphism in pre-microRNA-146a is associated with lung cancer risk in a Korean population

被引:50
作者
Jeon, Hyo-Sung [1 ,2 ]
Lee, Yong Hoon [3 ]
Lee, Shin Yup [2 ,3 ]
Jang, Ji-Ae [1 ]
Choi, Yi-Young [1 ]
Yoo, Seung Soo [2 ,3 ]
Lee, Won Kee [4 ]
Choi, Jin Eun [1 ,2 ]
Son, Ji Woong [5 ]
Kang, Young Mo [3 ]
Park, Jae Yong [1 ,2 ,3 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Taegu 700422, South Korea
[2] Kyungpook Natl Univ, Med Ctr, Lung Canc Ctr, Taegu 702210, South Korea
[3] Kyungpook Natl Univ, Sch Med, Dept Internal Med, Taegu 700422, South Korea
[4] Kyungpook Natl Univ, Sch Med, Ctr Stat, Taegu 700422, South Korea
[5] Konyang Univ Hosp, Dept Internal Med, Taejon 302718, South Korea
基金
新加坡国家研究基金会;
关键词
Lung cancer; Risk factor; miR-146a; MicroRNA; HUMAN MICRORNA GENES; FUNCTIONAL POLYMORPHISM; PROSTATE-CANCER; MIR-146A GENE; EXPRESSION; PRE-MIR-146A; CARCINOMA; CELLS; RS2910164; SEQUENCES;
D O I
10.1016/j.gene.2013.10.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Introduction: MicroRNAs (miRs) play important roles in the development and progression of human cancers. MiR-146a down-regulates epidermal growth factor receptor and the nuclear factor-kappa B regulatory kinase interleukin-1 receptor-associated kinase 1 genes that play important roles in lung carcinogenesis. This study was conducted to evaluate the association between rs2910164C>G, a functional polymorphism in the pre-miR-146a, and lung cancer risk. Material and methods: The rs2910164C>G genotypes were determined in 1094 patients with lung cancer and 1100 healthy controls who were frequency matched for age and gender. Results: The rs2910164 CG or GG genotype was associated with a significantly decreased risk for lung cancer compared to that of the CC genotype (adjusted odds ratio = 0.80, 95% confidence interval = 0.66-0.96, P = 0.02). When subjects were stratified according to smoking exposure (never, light and heavy smokers), the effect of the rs2910164C>G genotype on lung cancer risk was significant only in never smokers (adjusted odds ratio = 0.66, 95% confidence interval = 0.45-0.96, P = 0.03, under a dominant model for the C allele) and decreased as smoking exposure level increased (P-trend < 0.001). In line with this result, the level of miR-146a expression in the tumor tissues was significantly higher in the GC genotype than in the CC or CG genotype only in never-smokers (P = 0.02). Conclusions: These findings suggest that the rs2910164C>G in pre-miR-146a may contribute to genetic susceptibility to lung cancer, and that miR-146a might be involved in lung cancer development. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 71
页数:6
相关论文
共 39 条
[1]   Replication of results of genome-wide association studies on lung cancer susceptibility loci in a Korean population [J].
Bae, Eun Young ;
Lee, Shin Yup ;
Kang, Bong Kyoon ;
Lee, Eun Jin ;
Choi, Yi Young ;
Kang, Hyo-Gyoung ;
Choi, Jin Eun ;
Jeon, Hyo-Sung ;
Lee, Won Kee ;
Kam, Shin ;
Shin, Kyung Min ;
Jin, Guang ;
Yoo, Seung Soo ;
Lee, Jaehee ;
Cha, Seung Ick ;
Kim, Chang Ho ;
Jung, Tae Hoon ;
Park, Jae Yong .
RESPIROLOGY, 2012, 17 (04) :699-706
[2]   Phylogenetic shadowing and computational identification of human microRNA genes [J].
Berezikov, E ;
Guryev, V ;
van de Belt, J ;
Wienholds, E ;
Plasterk, RHA ;
Cuppen, E .
CELL, 2005, 120 (01) :21-24
[3]   Expression of microRNA-146 suppresses NF-κB activity with reduction of metastatic potential in breast cancer cells [J].
Bhaumik, D. ;
Scott, G. K. ;
Schokrpur, S. ;
Patil, C. K. ;
Campisi, J. ;
Benz, C. C. .
ONCOGENE, 2008, 27 (42) :5643-5647
[4]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[5]   miR-146a Inhibits Cell Growth, Cell Migration and Induces Apoptosis in Non-Small Cell Lung Cancer Cells [J].
Chen, Gang ;
Umelo, Ijeoma Adaku ;
Lv, Shasha ;
Teugels, Erik ;
Fostier, Karel ;
Kronenberger, Peter ;
Dewaele, Alex ;
Sadones, Jan ;
Geers, Caroline ;
De Greve, Jacques .
PLOS ONE, 2013, 8 (03)
[6]   MicroRNAs and cancer epigenetics: a macrorevolution [J].
Davalos, Veronica ;
Esteller, Manel .
CURRENT OPINION IN ONCOLOGY, 2010, 22 (01) :35-45
[7]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[8]   Regulatory mechanisms of microRNAs involvement in cancer: the strange case of Dr Jekyll and Mr Hyde [J].
Fabbri, Muller ;
Ivan, Mircea ;
Cimmino, Amelia ;
Negrini, Massimo ;
Calin, George A. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2007, 7 (07) :1009-1019
[9]   Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105
[10]   Down-regulation of BRCA1 expression by miR-146a and miR-146b-5p in triple negative sporadic breast cancers [J].
Garcia, Amandine I. ;
Buisson, Monique ;
Bertrand, Pascale ;
Rimokh, Ruth ;
Rouleau, Etienne ;
Lopez, Bernard S. ;
Lidereau, Rosette ;
Mikaelian, Ivan ;
Mazoyer, Sylvie .
EMBO MOLECULAR MEDICINE, 2011, 3 (05) :279-290