Association of polymorphisms and haplotypes of the NBN gene with laryngeal cancer and multiple primary tumors of the head and neck

Head and Neck

Volumn 34, Issue 3, 2012, Pages 376-383

  Ziółkowska Suchanek, Iwona ^a   Mosor, Maria ^a,b   Wierzbicka, Małgorzata ^c   Fichna, Marta ^a,c   Rydzanicz, Małgorzata ^a   Nowak, Jerzy ^a  

^a INSTITUTE OF HUMAN GENETICS   (Poland)

^b Foundation for Polish Science   (Poland)

^c POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

Author keywords

haplotype; laryngeal cancer; multiple primary tumors of head and neck; NBN gene; polymorphism

Indexed keywords

NIBRIN;

ADULT; ARTICLE; CANCER RISK; CONTROLLED STUDY; ESOPHAGUS TUMOR; FEMALE; GENE FREQUENCY; HAPLOTYPE; HEAD AND NECK TUMOR; HUMAN; JAW TUMOR; LARYNX CANCER; LIP TUMOR; LUNG TUMOR; MAJOR CLINICAL STUDY; MALE; MOUTH TUMOR; PAROTID GLAND TUMOR; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SKIN TUMOR; THYROID TUMOR; TONGUE TUMOR; TONSIL TUMOR;

ADULT; AGED; CASE-CONTROL STUDIES; CELL CYCLE PROTEINS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HEAD AND NECK NEOPLASMS; HUMANS; LARYNGEAL NEOPLASMS; MALE; MIDDLE AGED; NEOPLASMS, MULTIPLE PRIMARY; NUCLEAR PROTEINS; POLYMORPHISM, GENETIC;

EID: 84856964341     PISSN: 10433074     EISSN: 10970347     Source Type: Journal    
DOI: 10.1002/hed.21741     Document Type: Article

References (30)

1. Warren S, Gates O,. Multiple primary malignant tumors: survey of the literature and statistical study. Am J Cancer 1932; 16: 1358.
2. Cianfriglia F, Di Gregorio DA, Manieri A,. Multiple primary tumours in patients with oral squamous cell carcinoma. Oral Oncol 1999; 35: 157-163. (Pubitemid 29113058)
3. Miller DG, Tiwari R, Pathak S, Hopwood VL, Gilbert F, Hsu TC,. DNA repair and mutagen sensitivity in patients with triple primary cancers. Cancer Epidemiol Biomarkers Prev 1998; 7: 321-327. (Pubitemid 28354144)
4. Digweed M, Sperling K,. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks. DNA Repair (Amst) 2004; 3: 1207-1217. (Pubitemid 38997964)
5. Varon R, Vissinga C, Platzer M, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 1998; 93: 467-476. (Pubitemid 28232090)
6. Lee JH, Paull TT,. Direct activation of the ATM protein kinase by the Mre11/Rad50/Nbs1 complex. Science 2004; 304: 93-96. (Pubitemid 38451463)
7. Mosor M, Ziółkowska I, Pernak-Schwarz M, Januszkiewicz-Lewandowska D, Nowak J,. Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia. Leukemia 2006; 20: 1454-1456. (Pubitemid 44084066)
8. Steffen J, Varon R, Mosor M, et al. Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. Int J Cancer 2004; 111: 67-71. (Pubitemid 38859284)
9. Steffen J, Nowakowska D, Niwinska A, et al. Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland. Int J Cancer 2006; 119: 472-475.
10. Lu J, Wei Q, Bondy ML, et al. Polymorphisms and haplotypes of the NBS1 gene are associated with risk of sporadic breast cancer in non-Hispanic white women ≤55 years. Carcinogenesis 2006; 27: 2209-2216. (Pubitemid 44644809)
11. Lan Q, Shen M, Berndt SI, et al. Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. Lung Cancer 2005; 49: 317-323. (Pubitemid 41139144)
12. Medina PP, Ahrendt SA, Pollan M, Fernandez P, Sidransky D, Sanchez-Cespedes M,. Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations. Cancer Epidemiol Biomarkers Prev 2003; 12: 699-704. (Pubitemid 36993158)
13. Thirumaran RK, Bermejo JL, Rudnai P, et al. Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin. Carcinogenesis 2006; 27: 1676-1681. (Pubitemid 44288057)
14. Ziółkowska I, Mosor M, Wierzbicka M, Rydzanicz M, Pernak-Schwarz M, Nowak J,. Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene. Cancer Sci 2007; 98: 1701-1705. (Pubitemid 47487904)
15. Nowak J, Mosor M, Ziółkowska I, et al. Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours. Eur J Cancer 2008; 44: 627-630.
16. Mosor M, Ziółkowska I, Januszkiewicz-Lewandowska D, Nowak J,. Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia. Eur J Cancer 2008; 44: 2226-2232.
17. Zienolddiny S, Campa D, Lind H, et al. Polymorphisms of DNA repair genes and risk of non-small cell lung cancer. Carcinogenesis 2006; 27: 560-567. (Pubitemid 43372885)
18. Lu M, Lu J, Yang X, et al. Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis. BMC Cancer 2009; 9: 124.
19. Kuschel B, Auranen A, McBride S, et al. Variants in DNA double-strand break repair genes and breast cancer susceptibility. Hum Mol Genet 2002; 11: 1399-1407.
20. Millikan RC, Player JS, Decotret AR, Tse CK, Keku T,. Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk. Cancer Epidemiol Biomarkers Prev 2005; 14: 2326-2334. (Pubitemid 41437832)
21. Hsu HM, Wang HC, Chen ST, Hsu GC, Shen CY, Yu JC,. Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex. Cancer Epidemiol Biomarkers Prev 2007; 16: 2024-2032.
22. Försti A, Angelini S, Festa F, et al. Single nucleotide polymorphisms in breast cancer. Oncol Rep 2004; 11: 917-922.
23. Smith TR, Levine EA, Freimanis RI, et al. Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk. Carcinogenesis 2008; 29: 2132-2138.
24. Ryk C, Kumar R, Thirumaran RK, Hou SM,. Polymorphisms in the DNA repair genes XRCC1, APEX1, XRCC3 and NBS1, and the risk for lung cancer in never- and ever-smokers. Lung Cancer 2006; 54: 285-292. (Pubitemid 44634137)
25. Margulis V, Lin J, Yang H, Wang W, Wood CG, Wu X,. Genetic susceptibility to renal cell carcinoma: the role of DNA double-strand break repair pathway. Cancer Epidemiol Biomarkers Prev 2008; 17: 2366-2373.
26. Auranen A, Song H, Waterfall C, et al. Polymorphisms in DNA repair genes and epithelial ovarian cancer risk. Int J Cancer 2005; 117: 611-618. (Pubitemid 41504549)
27. Cerosaletti KM, Morrison VA, Sabat DE, Willerford DM, Concannon P,. Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma. Genes Chromosomes Cancer 2002; 35: 282-286.
28. Rollinson S, Kesby H, Morgan GJ,. Haplotypic variation in MRE11, RAD50 and NBS1 and risk of non-Hodgkin's lymphoma. Leuk Lymphoma 2006; 47: 2567-2583. (Pubitemid 44932647)
29. Park SL, Bastani D, Goldstein BY, et al. Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers. Carcinogenesis 2010; 31: 1264-1271.
30. Loizidou MA, Cariolou MA, Neuhausen SL, et al. Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population. Breast Cancer Res Treat 2010; 121: 147-156.