Functional polymorphisms of JWA gene are associated with risk of bladder cancer

被引:12
作者
Li, Chun-Ping
Zhu, Yu-Jie
Chen, Rui
Wu, Wei
Li, Ai-Ping
Liu, Jia
Liu, Qi-Zhan
Wei, Qing-Yi
Zhang, Zheng-Dong
Zhou, Jian-Wei
机构
[1] Nanjing Med Univ, Sch Publ Hlth, Dept Mol Cell Biol & Toxicol, Nanjing 210029, Peoples R China
[2] Univ Texas, MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2007年 / 70卷 / 11-12期
关键词
D O I
10.1080/15287390701285824
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The JWA gene is a novel cell differentiation-related gene thought to be a responsive gene in response to DNA damage and repair induced by enviromnental stressors. Recently, a novel single nucleotide polymorphism (SNP) was identified in the promoter of the JWA gene (-76G -> C) that may alter the transcription activity and thus play a role in increased risk of bladder cancer. Further, studies were conducted to screen for more novel variants in the JWA exons by using PCR-SSCP (polymerase chain reaction-single-strand conformation polymorphism) followed by PCR-RFLP (PCR restriction fragment length polymorphism) methods. Finally, the functional relevance of the newly identified genetic variants in a hospital-based case-control study of 215 bladder cancer patients and 250 cancer-free controls was evaluated. In addition to the -76G -> C polymorphism, another novel SNP (454C -> A in exon2 and 723T -> G in exon 3) of JWA was identified. The -76G -> C allele and genotype frequencies were found to vary in different ethnic groups. The -76C allele and 454A allele were both associated with significantly increased risk of bladder cancer. In contrast, the 723GG genotype was associated with a decreased risk of bladder cancer. Furthermore, -76C and 454A together increased the risk of bladder caner using haplotype and stratification analysis. In conclusion, the three novel functional genetic polymorphisms of JWA gene, -76G -> C, 454C -> A, and 723T -> G, appear to contribute to the etiology of bladder cancer.
引用
收藏
页码:876 / 884
页数:9
相关论文
共 33 条
[1]   PRA isoforms are targeted to distinct membrane compartments [J].
Abdul-Ghani, M ;
Gougeon, PY ;
Prosser, DC ;
Da-Silva, LF ;
Ngsee, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6225-6233
[2]   Variability in nucleotide excision repair and cancer risk: a review [J].
Benhamou, S ;
Sarasin, A .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 462 (2-3) :149-158
[3]   Protein oxidation in aging, disease, and oxidative stress [J].
Berlett, BS ;
Stadtman, ER .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20313-20316
[4]   Markers of DNA repair and susceptibility to cancer in humans: An epidemiologic review [J].
Berwick, M ;
Vineis, P .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (11) :874-897
[5]   A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans [J].
Bond, GL ;
Hu, WW ;
Bond, EE ;
Robins, H ;
Lutzker, SG ;
Arva, NC ;
Bargonetti, J ;
Bartel, F ;
Taubert, H ;
Wuerl, P ;
Onel, K ;
Yip, L ;
Hwang, SJ ;
Strong, LC ;
Lozano, G ;
Levine, AJ .
CELL, 2004, 119 (05) :591-602
[6]   Molecular cloning, gene structure, expression profile and functional characterization of the mouse glutamate transporter (EAAT3) interacting protein GTRAP3-18 [J].
Butchbach, MER ;
Lai, LC ;
Lin, CLG .
GENE, 2002, 292 (1-2) :81-90
[7]   Role of JWA in acute promyelocytic leukemia cell differentiation and apoptosis triggered by retinoic acid, 12-tetradecanoylphorbol-13-acetate and arsenic trioxide [J].
Cao, HX ;
Xia, W ;
Shen, Q ;
Lu, H ;
Ye, J ;
Li, AP ;
Zou, CP ;
Zhou, JW .
CHINESE SCIENCE BULLETIN, 2002, 47 (10) :834-838
[8]   MOLECULAR-CLONING OF YPT1/SEC4-RELATED CDNAS FROM AN EPITHELIAL-CELL LINE [J].
CHAVRIER, P ;
VINGRON, M ;
SANDER, C ;
SIMONS, K ;
ZERIAL, M .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) :6578-6585
[9]   Epidemiology and etiology of premalignant and malignant urothelial changes [J].
Cohen, SM ;
Shirai, T ;
Steineck, G .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 2000, 34 :105-115
[10]   Repair of oxidative damage to nuclear and mitochondrial DNA in mammalian cells [J].
Croteau, DL ;
Bohr, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (41) :25409-25412