Caspase 9 promoter polymorphisms and risk of primary lung cancer

被引:79
作者
Park, Jae Yong
Park, Jung Min
Jang, Jin Sung
Choi, Jin Eun
Kim, Kyung Mee
Cha, Sung Ick
Kim, Chang Ho
Kang, Young Mo
Lee, Won Kee
Kam, Sin
Park, Rang Woon
Kim, In San
Lee, Jae-Tae
Jung, Tae Hoon
机构
[1] Kyungpook Natl Univ, Sch Med, Canc Res Inst, Taegu 700412, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Nucl Med, Taegu 700412, South Korea
[3] Kyungpook Natl Univ, Sch Med, Dept Biochem, Taegu 700422, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Prevent Med, Taegu 700422, South Korea
[5] Kyungpook Natl Univ Hosp, Dept Internal Med, Taegu 700412, South Korea
关键词
D O I
10.1093/hmg/ddl119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspase-9 (CASP-9) is an initiator CASP in the apoptosome-driven apoptosis pathway and plays an important role in the development and progression of cancer. Polymorphisms in the promoter region of the CASP-9 gene may influence the promoter activity of this gene, thereby modulating susceptibility to lung cancer. To test this hypothesis, we examined the association of four polymorphisms [-1263A > G, -905T > G, -712C > T and -293_-275delCGTGAGGTCAGTGCGGGGA (-293del)] in the CASP-9 promoter with the risk of lung cancer in a Korean population. The CASP-9 genotypes were determined in 432 lung cancer patients and 432 healthy controls that were frequency-matched for age and gender. The -1263 GG genotype was associated with a significantly decreased risk of lung cancer compared with the -1263 AA genotype or combined -1263 AA + AG genotype [adjusted odds ratio (OR) = 0.64, 95% confidence interval (95% CI) = 0.42-0.98, P = 0.04 and adjusted OR = 0.67, 95% Cl = 0.46-0.97, P = 0.01, respectively]. For the -712C > T polymorphism, individuals with at least one -712T allele were at a significantly increased risk of lung cancer compared with those harboring the -712 CC genotype (adjusted OR = 1.42, 95% Cl = 1.06-1.89, P = 0.02). Consistent with the results of genotype analyses, the -1263G/-712C (G-C) haplotype was associated with a significantly decreased risk of lung cancer [adjusted OR = 0.59, 95% Cl = 0.47-0.75, P and Bonferroni corrected P (PC) < 0.001]. Moreover, the risk of lung cancer decreased in a dose-dependent manner as the number of the G-C haplotypes increased (adjusted OR = 0.60, 95% Cl = 0.45-0.81, P = 0.0007 and P-c = 0.0014 for the G-C heterozygotes and adjusted OR = 0.34, 95% Cl = 0.17-0.68, P = 0.0023 and P-c = 0.0046 for the G-C homozygotes; P-trend < 0.001). The promoter assay revealed the G-C haplotype to have a significantly higher promoter activity than the -1263G/-712T and -1263A/-712C haplotypes. These results suggest that CASP-9 promoter polymorphisms affect CASP-9 expression and contribute to genetic susceptibility to lung cancer.
引用
收藏
页码:1963 / 1971
页数:9
相关论文
共 45 条
[1]   The mitochondrial apoptosome: a killer unleashed by the cytochrome seas [J].
Adrain, C ;
Martin, SJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (06) :390-397
[2]   Apoptosis control by death and decoy receptors [J].
Ashkenazi, A ;
Dixit, VM .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :255-260
[3]   TRAIL receptor-2 signals apoptosis through FADD and caspase-8 [J].
Bodmer, JL ;
Holler, N ;
Reynard, S ;
Vinciguerra, P ;
Schneider, P ;
Juo, P ;
Blenis, J ;
Tschopp, J .
NATURE CELL BIOLOGY, 2000, 2 (04) :241-243
[4]   Biochemical pathways of caspase activation during apoptosis [J].
Budihardjo, I ;
Oliver, H ;
Lutter, M ;
Luo, X ;
Wang, XD .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 :269-290
[5]   A decade of caspases [J].
Degterev, A ;
Boyce, M ;
Yuan, JY .
ONCOGENE, 2003, 22 (53) :8543-8567
[6]   Population aspects of cancer genetics [J].
Goldgar, DE .
BIOCHIMIE, 2002, 84 (01) :19-25
[7]  
Grabe Niels, 2002, In Silico Biology, V2, pS1
[8]   Apoptosome dysfunction in human cancer [J].
Hajra, KM ;
Liu, JR .
APOPTOSIS, 2004, 9 (06) :691-704
[9]   Cigarette smoking and lung cancer: chemical mechanisms and approaches to prevention [J].
Hecht, SS .
LANCET ONCOLOGY, 2002, 3 (08) :461-469
[10]   The regulation of APAF1 expression during development and tumourigenesis [J].
Hickman, ES ;
Helin, K .
APOPTOSIS, 2002, 7 (02) :167-171