Association of single nucleotide polymorphisms of nbsl gene with genetic susceptibility to primary liver cancer in a chinese han population

Progress in Biochemistry and Biophysics

Volumn 39, Issue 7, 2012, Pages 678-686

  Huang, Jian ^a,b,c   Zhao, Yan Ping ^a,b,c   Li, Qian ^a,b,c   Zhang, Jun Xia ^a,b,c   Wang, Yan ^a,b,c   Zhang, Bei ^a,b,c  

^a CAPITAL MEDICAL UNIVERSITY   (China)

^b Tianjin Infectious Disease Specialty Hospital   (China)

^c PEKING UNION MEDICAL COLLEGE   (China)

Author keywords

Genetic susceptibility; High resolution sscp analysis; NBSl; Primary liver cancer; Single nucleotide polymorphisms

Indexed keywords

EID: 84867083547     PISSN: 10003282     EISSN: None     Source Type: Journal    
DOI: 10.3724/SP.J.1206.2011.00536     Document Type: Article

References (15)

1. Zhang Y, Zhou J Q, Chang UK Lim. The role of NBSl in DNA double strand break repair, telomere stability, and cell cycle checkpoint control. Cell Res, 2006,16(1): 45-54 (Pubitemid 43129308)
2. Paulli M, Viglio A, Bovcri E, et al. Nijmegen breakage syndromeassociated T-ccll-rich B-cell lymphoma: Case report. Pediatr Dev Pathol, 2000,3(3): 264-270 (Pubitemid 30232852)
3. Kruger L, Demuth I, Neitzel H, el al. Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein. Carcinogenesis, 2007,28(1): 107-111 (Pubitemid 44942632)
4. Dumon-Jones, Frappart P O, Tong W M, et al. Mice heterozygous for NBN (the murine homologue of NBSl) developed a wide variety of tumors affecting the liver, mammary gland, prostate, and lung, in addition to lymphomas. Cancer Res, 2003, 63(21): 7263-7269
5. Mosor M, Ziokowska I, Januszkiewicz D, et al. Polymorphisms and haplotypes of the NBSl gene in childhood acute leukaemia. Eur J Cancer, 2008,44(15): 2226 -2232
6. Lan Q, Shen M, Bemdt S I, el al. Smoky coal exposure, NBSl polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. Lung Cancer, 2005,49(3): 317-323 (Pubitemid 41139144)
7. Lu J, Wei Q, Bondy M L, et al. Polymorphisms and haplotypes of the NBSl gene are associated with risk of sporadic breast cancer in non-Hispanic white women
8. ZiAllkowska I, Mosor M, Wierzbicka M, et al. Increased risk of larynx cancer in heterozygous carriers of the 1171V mutation of the NBSl gene. Cancer Sei, 2007,98(11): 1701-1705
9. Sanyal S, Festa F, Sakano S, et al. Polymorphisms in DNA repair and metabolic genes in bladder cancer. Carcinogenesis, 2004, 25(5): 729-734 (Pubitemid 38618524)
10. Watanabe T, Nobusawa S, Lu S Q, et al. Mutational inactivation of the Nijmegen breakage syndrome gene (NBSl) in glioblastomas is associated with multiple TP53 mutations. J Neuropath Exp Neur, 2009,68(2): 210-215
11. Thorgcirsson S S, Grisham T W. Molecular pathogenesis of human hepatocellular carcinoma. Nat Genet, 2002,31(4): 339-346
12. Bai X L, Sun L P, Liu J, et al. Chin J Cancer, 2008,27(1): 35-40
13. Huang J, Grotzcr M A, Watanabe T, et al. Mutations in the Nijmegen breakage syndrome gene in medutloblastomas. Clin Cancer Res, 2008,14(13): 4053-4058
14. [i4] Zhu D Q, Huang Z Y. World Chin J Digestology, 2007, 15(16): 1775-1780
15. Patcrlini-Brechot P, Saigo K, Murakami Y, et al. Hepatitis B virus related insertional mutagenesis occurs frequently in human liver cancers and recurrently targets human telomerase gene. Oncogene, 2003,22(25): 3911-3916 (Pubitemid 36819664)