Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893–917.
CAS
PubMed
Article
Google Scholar
Khanna KK, Jackson SP. DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet. 2001;27:247–54.
CAS
PubMed
Article
Google Scholar
Scott SP, Pandita TK. The cellular control of DNA double-strand breaks. J Cell Biochem. 2006;99:1463–75.
CAS
PubMed Central
PubMed
Article
Google Scholar
Bernstein KA, Rothstein R. At loose ends: resecting a double-strand break. Cell. 2009;137:807–10.
CAS
PubMed
Article
Google Scholar
Taylor EM, Cecillon SM, Bonis A, Chapman JR, Povirk LF, Lindsay HD. The Mre11/Rad50/Nbs1 complex functions in resection-based DNA end joining in Xenopus laevis. Nucleic Acids Res. 2010;38:441–54.
CAS
PubMed Central
PubMed
Article
Google Scholar
Dzikiewicz-Krawczyk A. The importance of making ends meet: mutations in genes and altered expression of proteins of the MRN complex and cancer. Mutat Res, Rev Mutat Res. 2008;659:262–73.
CAS
Article
Google Scholar
Paull TT, Gellert M. Nbs1 potentiates ATP-driven DNA unwinding and endonuclease cleavage by the Mre11/Rad50 complex. Genes Dev. 1999;13:1276–88.
CAS
PubMed
Article
Google Scholar
Lamarche BJ, Orazio NI, Weitzman MD. The MRN complex in double-strand break repair and telomere maintenance. FEBS Letters.584:3682–95.
Matsuura S, Tauchi H, Nakamura A, Kondo N, Sakamoto S, Endo S, et al. Positional cloning of the gene for Nijmegen breakage syndrome. Nat Genet. 1998;19:179–81.
CAS
PubMed
Article
Google Scholar
Carney JP, Maser RS, Olivares H, Davis EM, Le Beau M, Yates 3rd JR, et al. The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. Cell. 1998;93:477–86.
CAS
PubMed
Article
Google Scholar
Dumon-Jones V, Frappart PO, Tong WM, Sajithlal G, Hulla W, Schmid G, et al. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis. Cancer Res. 2003;63:7263–9.
CAS
PubMed
Google Scholar
di Masi A, Antoccia A. NBS1 heterozygosity and cancer risk. Curr Genomics. 2008;9:275–81.
PubMed
Article
Google Scholar
Forsti A, Angelini S, Festa F, Sanyal S, Zhang Z, Grzybowska E, et al. Single nucleotide polymorphisms in breast cancer. Oncol Rep. 2004;11:917–22.
PubMed
Google Scholar
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 (Amsterdam, Netherlands). 2006;54:285–92.
Article
Google Scholar
Broberg K, Bjork J, Paulsson K, Hoglund M, Albin M. Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer. Carcinogenesis. 2005;26:1263–71.
CAS
PubMed
Article
Google Scholar
Hebbring SJ, Fredriksson H, White KA, Maier C, Ewing C, McDonnell SK, et al. Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer. Cancer Epidemiol, Biomark Prev. 2006;15:935–8.
CAS
Article
Google Scholar
Gil J, Ramsey D, Stembalska A, Karpinski P, Pesz KA, Laczmanska I, et al. The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer. Mol Biol Rep. 2012;39:527–34.
CAS
PubMed
Article
Google Scholar
Li N, Xu Y, Zheng J, Jiang L, You Y, Wu H, et al. NBS1 rs1805794G>C polymorphism is associated with decreased risk of acute myeloid leukemia in a Chinese population. Mol Biol Rep. 2013;40:3749–56.
CAS
PubMed
Article
Google Scholar
Zheng J, Zhang C, Jiang L, You Y, Liu Y, Lu J, et al. Functional NBS1 polymorphism is associated with occurrence and advanced disease status of nasopharyngeal carcinoma. Mol Carcinog. 2011;50:689–96.
CAS
PubMed
Article
Google Scholar
Lu M, Lu J, Yang X, Yang M, Tan H, Yun B, et al. Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis. BMC Cancer. 2009;9:124.
PubMed Central
PubMed
Article
Google Scholar
Zhang Y, Zhang J, Deng Y, Tian C, Li X, Huang J, et al. Polymorphisms in the cytotoxic T-lymphocyte antigen 4 gene and cancer risk: a meta-analysis. Cancer. 2011;117:4312–24.
CAS
PubMed
Article
Google Scholar
Desjardins S, Beauparlant JC, Labrie Y, Ouellette G, Durocher F, BRCAs I. Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer. BMC cancer. 2009;9.
Jelonek K, Gdowicz-Klosok A, Pietrowska M, Borkowska M, Korfanty J, Rzeszowska-Wolny J, et al. Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population. J Appl Genet. 2010;51:343–52.
CAS
PubMed
Article
Google Scholar
Kuschel B, Auranen A, McBride S, Novik KL, Antoniou A, Lipscombe JM, et al. Variants in DNA double-strand break repair genes and breast cancer susceptibility. Hum Mol Genet. 2002;11:1399–407.
CAS
PubMed
Article
Google Scholar
Loizidou MA, Cariolou MA, Neuhausen SL, Newbold RF, Bashiardes E, Marcou Y, et al. Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population. Breast Cancer Res Treatment. 2010;121:147–56.
CAS
Article
Google Scholar
Lu J, Wei Q, Bondy ML, Li D, Brewster A, Shete S, 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;27:2209–16.
CAS
PubMed
Article
Google Scholar
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 Biomark Prev. 2005;14:2326–34.
CAS
Article
Google Scholar
Silva SN, Tomar M, Paulo C, Gomes BC, Azevedo AP, Teixeira V, et al. Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51. Cancer Epidemiol. 2010;34:85–92.
CAS
PubMed
Article
Google Scholar
Smith TR, Levine EA, Freimanis RI, Akman SA, Allen GO, Hoang KN, et al. Polygenic model of DNA repair genetic polymorphisms in human breast cancer risk. Carcinogenesis. 2008;29:2132–8.
CAS
PubMed
Article
Google Scholar
Zhang L, Zhang Z, Yan W. Single nucleotide polymorphisms for DNA repair genes in breast cancer patients. Clin Chim Acta. 2005;359:150–5.
CAS
PubMed
Article
Google Scholar
Tarasov VA, Aslanyan MM, Tsyrendorzhiyeva ES, Litvinov SS, Gar'kavtseva RF, Altukhov YP. Genetically determined subdivision of human populations with respect to the risk of breast cancer in women. Doklady Biol Sci. 2006;406:66–9.
CAS
Article
Google Scholar
Auranen A, Song H, Waterfall C, Dicioccio RA, Kuschel B, Kjaer SK, et al. Polymorphisms in DNA repair genes and epithelial ovarian cancer risk. Int J Cancer. 2005;117:611–8.
CAS
PubMed
Article
Google Scholar
Choudhury A, Elliott F, Iles MM, Churchman M, Bristow RG, Bishop DT, et al. Analysis of variants in DNA damage signalling genes in bladder cancer. BMC Med Genet. 2008;9:69.
PubMed Central
PubMed
Article
Google Scholar
Figueroa JD, Malats N, Rothman N, Real FX, Silverman D, Kogevinas M, et al. Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk. Carcinogenesis. 2007;28:1788–93.
CAS
PubMed
Article
Google Scholar
Sanyal S, Festa F, Sakano S, Zhang Z, Steineck G, Norming U, et al. Polymorphisms in DNA repair and metabolic genes in bladder cancer. Carcinogenesis. 2004;25:729–34.
CAS
PubMed
Article
Google Scholar
Jiao J, Zheng T, Lan Q, Chen Y, Deng Q, Bi X, et al. Occupational solvent exposure, genetic variation of DNA repair genes, and the risk of non-Hodgkin's lymphoma. Eur J Cancer Prev. 2012;21:580–4.
CAS
PubMed Central
PubMed
Article
Google Scholar
Mosor M, Ziolkowska I, Januszkiewicz-Lewandowska D, Nowak J. Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia. Eur JCancer (Oxford). 2008;44:2226–32.
CAS
Google Scholar
Lan Q, Shen M, Berndt SI, Bonner MR, He X, Yeager M, et al. Smoky coal exposure, NBS1 polymorphisms, p53 protein accumulation, and lung cancer risk in Xuan Wei, China. Lung Cancer (Amsterdam, Netherlands). 2005;49:317–23.
Article
Google Scholar
Zienolddiny S, Campa D, Lind H, Ryberg D, Skaug V, Stangeland L, et al. Polymorphisms of DNA repair genes and risk of non-small cell lung cancer. Carcinogenesis. 2006;27:560–7.
CAS
PubMed
Article
Google Scholar
Pardini B, Naccarati A, Novotny J, Smerhovsky Z, Vodickova L, Polakova V, et al. repair genetic polymorphisms and risk of colorectal cancer in the Czech Republic. Mutation Res. 2008;638:146–53.
CAS
PubMed
Article
Google Scholar
Bastos HN, Antao MR, Silva SN, Azevedo AP, Manita I, Teixeira V, et al. Association of polymorphisms in genes of the homologous recombination DNA repair pathway and thyroid cancer risk. Thyroid. 2009;19:1067–75.
CAS
PubMed
Article
Google Scholar
Festa F, Kumar R, Sanyal S, Unden B, Nordfors L, Lindholm B, et al. Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism. Mutation Res. 2005;574:105–11.
CAS
PubMed
Article
Google Scholar
Huang MD, Chen XF, Xu G, Wu QQ, Zhang JH, Chen GF, et al. Genetic variation in the NBS1 gene is associated with hepatic cancer risk in a Chinese population. DNA Cell Biol. 2012;31:678–82.
CAS
PubMed
Article
Google Scholar
Schuetz JM, MaCarthur AC, Leach S, Lai AS, Gallagher RP, Connors JM, et al. Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma. BMC Med Genet. 2009;10:117.
PubMed Central
PubMed
Article
Google Scholar
Ziolkowska 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;98:1701–5.
CAS
PubMed
Article
Google Scholar
Thirumaran RK, Bermejo JL, Rudnai P, Gurzau E, Koppova K, Goessler W, et al. Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin. Carcinogenesis. 2006;27:1676–81.
CAS
PubMed
Article
Google Scholar
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, Biomark Prev. 2008;17:2366–73.
CAS
Article
Google Scholar
Cancer Genome Atlas N. Comprehensive molecular portraits of human breast tumours. Nat Geosci. 2012;490:61–70.
Google Scholar
Wei Q, Cheng L, Amos CI, Wang LE, Guo Z, Hong WK, et al. Repair of tobacco carcinogen-induced DNA adducts and lung cancer risk: a molecular epidemiologic study. J Nat Cancer Inst. 2000;92:1764–72.
CAS
PubMed
Article
Google Scholar