Jia YM, Xie YT, Wang YJ, Han JY, Tian XX, Fang WG. Association of genetic polymorphisms in cdh1 and ctnnb1 with breast cancer susceptibility and patients’ prognosis among chinese han women. PLoS One. 2015;10:e0135865.
Article
Google Scholar
Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90.
Article
Google Scholar
Sirisena ND, Dissanayake VHW. Cancer genetics and the surgeon – new frontiers. Sri Lanka J Surg. 2014;32(2):12–9.
Article
Google Scholar
Bell DW, Kim SH, Godwin AK, Schiripo TA, Harris PL, Haserlat SM, Wahrer DCR, Haiman CA, Daly MB, Niendorf KB, Smith MM, Sgroi DC, Garber JE, Olopade OI, Le Marchand L, Henderson BE, Altshuler D, Haber DA, Freedman ML. Genetic and functional analysis of chek2 (chk2) variants in multiethnic cohorts. Int J Cancer. 2007;121:2661–7.
Article
CAS
Google Scholar
Deng Z, Yang H, Liu Q, Wang Z, Feng T, Ouyang Y, Jin T, Ren H. Identification of novel susceptibility markers for the risk of overall breast cancer as well as subtypes defined by hormone receptor status in the chinese population. J Hum Genet. 2016;61:1027–34.
Article
CAS
Google Scholar
Loizidou MA, Michael T, Neuhausen SL, Newbold RF, Marcou Y, Kakouri E, Daniel M, Papadopoulos P, Malas S, Kyriacou K, Hadjisavvas A. Genetic polymorphisms in the dna repair genes xrcc1, xrcc2 and xrcc3 and risk of breast cancer in cyprus. Breast Cancer Res Treat. 2008;112:575–9.
Article
CAS
Google Scholar
Long J, Cai Q, Shu X-O, Qu S, Li C, Zheng Y, Gu K, Wang W, Xiang YB, Cheng J, Chen K, Zhang L, Zheng H, Shen CY, Huang C-S, Hou MF, Shen H, Hu Z, Wang F, Deming SL, Kelley MC, Shrubsole MJ, Khoo US, Chan KYK, Chan SY, Haiman CA, Henderson BE, Le Marchand L, Iwasaki M, Kasuga Y, et al. Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the asia breast cancer consortium. PLoS Genet. 2010;6:e1001002.
Article
Google Scholar
Mavaddat N, Pharoah PD, Michailidou K, Tyrer J, Brook MN, Bolla MK, Wang Q, Dennis J, Dunning AM, Shah M, Luben R, Brown J, Bojesen SE, Nordestgaard BG, Nielsen SF, Flyger H, Czene K, Darabi H, Eriksson M, Peto J, Dos-Santos-Silva I, Dudbridge F, Johnson N, Schmidt MK, Broeks A, Verhoef S, Rutgers EJ, Swerdlow A, Ashworth A, Orr N, et al. Prediction of breast cancer risk based on profiling with common genetic variants. J Natl Cancer Inst. 2015;107
Gaudet MM, Kuchenbaecker KB, Vijai J, Klein RJ, Kirchhoff T, Mcguffog L, Barrowdale D, Dunning AM, Lee A, Dennis J, Healey S, Dicks E, Soucy P, Sinilnikova OM, Pankratz VS, Wang X, Eldridge RC, Tessier DC, Vincent D, Bacot F, Hogervorst FBL, Peock S, Stoppa-Lyonnet D, KConFab Investigators, Peterlongo P, Schmutzler RK, Nathanson KL, Piedmonte M, Singer CF, Thomassen M, et al. Identification of a brca2-specific modifier locus at 6p24 related to breast cancer risk. Plos Genet. 2013;9:e1003173.
Article
CAS
Google Scholar
Easton DF, Pooley KA, Dunning AM, Pharoah PDP, Thompson D, Ballinger DG, Struewing JP, Morrison J, Field H, Luben R, Wareham N, Ahmed S, Healey CS, Bowman R, SEARCH Collaborators, Meyer KB, Haiman CA, Kolonel LK, Henderson BE, Le Marchand L, Brennan P, Sangrajrang S, Gaborieau V, Odefrey F, Shen CY, Wu PE, Wang HC, Eccles D, Evans DG, Peto J, et al. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature. 2007;447:1087–93.
Article
CAS
Google Scholar
Michailidou K, Hall P, Gonzalez-Neira A, Ghoussaini M, Dennis J, Milne RL, Schmidt MK, Chang-Claude J, Bojesen SE, Bolla MK, Wang Q, Dicks E, Lee A, Turnbull C, Rahman N, Breast and Ovarian Cancer Susceptibility Collaboration, Fletcher O, Peto J, Gibson L, Dos Santos Silva I, Nevanlinna H, Muranen TA, Aittomäki K, Blomqvist C, Czene K, Irwanto A, Liu J, Waisfisz Q, Meijers-Heijboer H, Adank M, et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet. 2013;45:353–61. 361e1
Article
CAS
Google Scholar
Mazhar A, Jamil F, Bashir Q, Ahmad MS, Masood M, Tanvir I, Rashid N, Waheed A, Afzal MN, Tariq MA. Genetic variants in fgfr2 and tnrc9 genes are associated with breast cancer risk in pakistani women. Mol Med Report. 2016;14:3443–51.
Article
CAS
Google Scholar
De Silva W, Karunanayake EH, Tennekoon KH, Allen M, Amarasinghe I, Angunawala P, Ziard MH. Novel sequence variants and a high frequency of recurrent polymorphisms in brca1 gene in sri lankan breast cancer patients and at risk individuals. BMC Cancer. 2008;8:214.
Article
Google Scholar
De Silva S, Tennekoon KH, Karunanayake EH, De Silva W, Amarasinghe I, Angunawela P. Novel sequence variants and common recurrent polymorphisms of brca2 in sri lankan breast cancer patients and a family with brca1 mutations. Exp Ther Med. 2011;2:1163–70.
Article
CAS
Google Scholar
De Silva S, Tennekoon KH, Karunanayake EH, Amarasinghe I, Angunawela P. Analysis of brca1 and brca2 large genomic rearrangements in sri lankan familial breast cancer patients and at risk individuals. BMC Res Notes. 2014;7:344.
Article
Google Scholar
Haiman CA, Stram DO, Pike MC, Kolonel LN, Burtt NP, Altshuler D, Hirschhorn J, Henderson BE. A comprehensive haplotype analysis of cyp19 and breast cancer risk: the multiethnic cohort. Hum Mol Genet. 2003;12:2679–92.
Article
CAS
Google Scholar
Gauderman WJ. Sample size requirements for association studies of gene-gene interaction. Am J Epidemiol. 2002;155:478–84.
Article
Google Scholar
Wigginton JE, Cutler DJ, Abecasis GR. A note on exact tests of hardy-weinberg equilibrium. Am J Hum Genet. 2005;76:887–93.
Article
CAS
Google Scholar
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira M, Bender D, Maller J, Sklar P, De Bakker P, Daly M, Sham P. Plink: a toolset for whole-genome association and population-based linkage analysis. Am J Hum Genet. 2007;81(3):559–75.
Article
CAS
Google Scholar
Silva SN, Tomar M, Paulo C, Gomes BC, Azevedo AP, Teixeira V, Pina JE, Rueff J, Gaspar JF. 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.
Article
CAS
Google Scholar
Yu KD, Chen AX, Qiu LX, Fan L, Yang C, Shao ZM. Xrcc2 arg188his polymorphism is not directly associated with breast cancer risk: evidence from 37,369 subjects. Breast Cancer Res Treat. 2010;123:219–25.
Article
CAS
Google Scholar
Pelttari LM, Kiiski JI, Ranta S, Vilske S, Blomqvist C, Aittomäki K, Nevanlinna H. Rad51, xrcc3, and xrcc2 mutation screening in finnish breast cancer families. Springerplus. 2015;4:92.
Article
Google Scholar
Pooley KA, Baynes C, Driver KE, Tyrer J, Azzato EM, Pharoah PDP, Easton DF, Ponder BAJ, Dunning AM. Common single-nucleotide polymorphisms in dna double-strand break repair genes and breast cancer risk. Cancer Epidemiol Biomark Prev. 2008;17:3482–9.
Article
CAS
Google Scholar
Lee KM, Choi JY, Kang C, Kang CP, Park SK, Cho H, Cho DY, Yoo KY, Noh DY, Ahn SH, Park C-G, Wei Q, Kang D. Genetic polymorphisms of selected dna repair genes, estrogen and progesterone receptor status, and breast cancer risk. Clin Cancer Res. 2005;11:4620–6.
Article
CAS
Google Scholar
Webb PM, Hopper JL, Newman B, Chen X, Kelemen L, Giles GG, Southey MC, Chenevix-Trench G, Spurdle AB. Double-strand break repair gene polymorphisms and risk of breast or ovarian cancer. Cancer Epidemiol Biomark Prev. 2005;14:319–23.
Article
CAS
Google Scholar
Kuschel B, Auranen A, Mcbride S, Novik KL, Antoniou A, Lipscombe JM, Day NE, Easton DF, Ponder BAJ, Pharoah PDP, Dunning A. Variants in dna double-strand break repair genes and breast cancer susceptibility. Hum Mol Genet. 2002;11:1399–407.
Article
CAS
Google Scholar
García-Closas M, Egan KM, Newcomb PA, Brinton LA, Titus-Ernstoff L, Chanock S, Welch R, Lissowska J, Peplonska B, Szeszenia-Dabrowska N, Zatonski W, Bardin-Mikolajczak A, Struewing JP. Polymorphisms in dna double-strand break repair genes and risk of breast cancer: two population-based studies in usa and poland, and meta-analyses. Hum Genet. 2006;119:376–88.
Article
Google Scholar
Kong B, Lv ZD, Chen L, Shen RW, Jin LY, Yang ZC. Lack of an association between xrcc2 r188h polymorphisms and breast cancer: an update meta-analysis involving 35,422 subjects. Int J Clin Exp Med. 2015;8:15808–14.
CAS
PubMed
PubMed Central
Google Scholar
Xu K, Song X, Chen Z, Qin C, He Y. Xrcc2 rs3218536 polymorphism decreases the sensitivity of colorectal cancer cells to poly (adp-ribose) polymerase 1 inhibitor. Oncol Lett. 2014;8:1222–8.
Article
CAS
Google Scholar
Hilbers FS, Luijsterburg MS, Wiegant WW, Meijers CM, Völker-Albert M, Boonen RA, Van Asperen CJ, Devilee P, Van Attikum H. Functional analysis of missense variants in the putative breast cancer susceptibility gene xrcc2. Hum Mutat. 2016;37:914–25.
Article
CAS
Google Scholar
Brooks J, Shore RE, Zeleniuch-Jacquotte A, Currie D, Afanasyeva Y, Koenig KL, Arslan AA, Toniolo P, Wirgin I. Polymorphisms in rad51, xrcc2, and xrcc3 are not related to breast cancer risk. Cancer Epidemiol Biomark Prev. 2008;17:1016–9.
Article
CAS
Google Scholar
Rafii S, O’Regan P, Xinarianos G, Azmy I, Stephenson T, Reed M, Meuth M, Thacker J, Cox A. A potential role for the xrcc2 r188h polymorphic site in dna-damage repair and breast cancer. Hum Mol Genet. 2002;11:1433–8.
Article
CAS
Google Scholar
Jiao L, Hassan MM, Bondy ML, Wolff RA, Evans DB, Abbruzzese JL, Li D. Xrcc2 and xrcc3 gene polymorphism and risk of pancreatic cancer. Am J Gastroenterol. 2008;103:360–7.
Article
CAS
Google Scholar
Jakubowska A, Rozkrut D, Antoniou A, Hamann U, Scott RJ, Mcguffog L, Healy S, Sinilnikova OM, Rennert G, Lejbkowicz F, Flugelman A, Andrulis IL, Glendon G, Ozcelik H, OCGN, Thomassen M, Paligo M, Aretini P, SWE-BRCA, Kantala J, Aroer B, Von Wachenfeldt A, Liljegren A, Loman N, Herbst K, Kristoffersson U, Rosenquist R, Karlsson P, Stenmark-Askmalm M, Melin B, et al. Association of phb 1630 c>t and mthfr 677 c>t polymorphisms with breast and ovarian cancer risk in brca1/2 mutation carriers: results from a multicenter study. Br J Cancer. 2012;106:2016–24.
Article
CAS
Google Scholar
Leal MF, Cirilo PD, Mazzotti TK, Calcagno DQ, Wisnieski F, Demachki S, Martinez MC, Assumpção PP, Chammas R, Burbano RR, Smith MC. Prohibitin expression deregulation in gastric cancer is associated with the 3′ untranslated region 1630 c>t polymorphism and copy number variation. PLoS One. 2014;9:e98583.
Article
Google Scholar
Manjeshwar S, Branam DE, Lerner MR, Brackett DJ, Jupe ER, Tumor suppression by the prohibitin gene 3’untranslated region rna in human breast cancer. Cancer Res. 2003;63:5251–6.
Webster LR, Provan PJ, Graham DJ, Byth K, Walker RL, Davis S, Salisbury EL, Morey AL, Ward RL, Hawkins NJ, Clarke CL, Meltzer PS, Balleine RL. Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33. Pathology. 2013;45:629–36.
Article
CAS
Google Scholar
Najm MZ, Akhtar MS, Ahmad I, Sadaf S, Mallick MN, Kausar MA, Chattopadhyay S, Ahad A, Zaidi S, Husain SA, Siddiqui WA. Mutational analysis of prohibitin - a highly conserved gene in indian female breast cancer cases. Asian Pac J Cancer Prev. 2012;13:5113–7.
Article
Google Scholar
Jakubowska A, Jaworska K, Cybulski C, Janicka A, Szymańska-Pasternak J, Lener M, Narod SA, Lubiński J, IHCC-Breast Cancer Study Group. Do brca1 modifiers also affect the risk of breast cancer in non-carriers? Eur J Cancer. 2009;45:837–42.
Article
CAS
Google Scholar
Jupe ER, Badgett AA, Neas BR, Craft MA, Mitchell DS, Resta R, Mulvihill JJ, Aston CE, Thompson LF. Single nucleotide polymorphism in prohibitin 3’untranslated region and breast-cancer susceptibility. Lancet. 2001;357:1588–9.
Article
CAS
Google Scholar
Karakus N, Kara N, Ulusoy AN. Lack of association between prohibitin 3’untranslated region c>t polymorphism and breast cancer in a turkish population. DNA Cell Biol. 2008;27:449–52.
Article
CAS
Google Scholar
Spurdle AB, Hopper JL, Chen X, MRE M, Giles GG, Newman B, Chenevix-Trench G. Prohibitin 3’untranslated region polymorphism and breast cancer risk in australian women. Lancet. 2002;360:925–6.
Article
CAS
Google Scholar
Beeghly-Fadiel A, Lu W, Gao Y-T, Long J, Deming SL, Cai Q, Zheng Y, Shu X, Zheng W. E-cadherin polymorphisms and breast cancer susceptibility: a report from the shanghai breast cancer study. Breast Cancer Res Treat. 2010;121:445–52.
Article
CAS
Google Scholar
Zhao L, Gu A, Ji G, Zou P, Zhao P, Lu A. The association between atm ivs 22–77 t>c and cancer risk: a meta-analysis. PLoS One. 2012;7:e29479.
Article
CAS
Google Scholar
Mehdipour P, Mahdavi M, Mohammadi-Asl J, Atri M. Importance of atm gene as a susceptible trait: predisposition role of d1853n polymorphism in breast cancer. Med Oncol. 2011;28:733–7.
Article
CAS
Google Scholar
Schrauder M, Frank S, Strissel PL, Lux MP, Bani MR, Rauh C, Sieber CC, Heusinger K, Hartmann A, Schulz-Wendtland R, Strick R, Beckmann MW, Fasching PA. Single nucleotide polymorphism d1853n of the atm gene may alter the risk for breast cancer. J Cancer Res Clin Oncol. 2008;134:873–82.
Article
CAS
Google Scholar
Gao LB, Xm P, Sun H, Wang X, Rao L, Li LJ, Liang WB, Lv ML, Yang WZ, Zhang L. The association between atm d1853n polymorphism and breast cancer susceptibility: a meta-analysis. J Exp Clin Cancer Res. 2010;29:117.
Article
Google Scholar
Concannon P, Haile RW, Børresen-Dale AL, Rosenstein BS, Gatti RA, Teraoka SN, Diep TA, Jansen L, Atencio DP, Langholz B, Capanu M, Liang X, Begg CB, Thomas DC, Bernstein L, Olsen JH, Malone KE, Lynch CF, Anton-Culver H, Bernstein JL. Variants in the atm gene associated with a reduced risk of contralateral breast cancer. Cancer Res. 2008;68:6486–91.
Article
CAS
Google Scholar