Skip to main content
Top
Published in: Breast Cancer Research 2/2007

Open Access 01-12-2007 | Research article

Identification of women with an increased risk of developing radiation-induced breast cancer: a case only study

Authors: Annegien Broeks, Linde M Braaf, Angelina Huseinovic, Anke Nooijen, Jos Urbanus, Frans BL Hogervorst, Marjanka K Schmidt, Jan GM Klijn, Nicola S Russell, Flora E Van Leeuwen, Laura J Van 't Veer

Published in: Breast Cancer Research | Issue 2/2007

Login to get access

Abstract

Introduction

Radiation exposure at a young age is one of the strongest risk factors for breast cancer. Germline mutations in genes involved in the DNA-damage repair pathway (DDRP) may render women more susceptible to radiation-induced breast cancer.

Methods

We evaluated the contribution of germline mutations in the DDRP genes BRCA1, BRCA2, CHEK2 and ATM to the risk of radiation-induced contralateral breast cancer (CBC). The germline mutation frequency was assessed, in a case-only study, in women who developed a CBC after they had a first breast cancer diagnosed before the age of 50 years, and who were (n = 169) or were not (n = 78) treated with radiotherapy for their first breast tumour.

Results

We identified 27 BRCA1, 5 BRCA2, 15 CHEK2 and 4 truncating ATM germline mutation carriers among all CBC patients tested (21%). The mutation frequency was 24.3% among CBC patients with a history of radiotherapy, and 12.8% among patients not irradiated for the first breast tumour (odds ratio 2.18 (95% confidence interval 1.03 to 4.62); p = 0.043). The association between DDRP germline mutation carriers and risk of radiation-induced CBC seemed to be strongest in women who developed their second primary breast tumour at least 5 years after radiotherapy. Those patients had an odds ratio of 2.51 (95% confidence interval 1.03 to 6.10; p = 0.049) of developing radiation-induced breast cancer, in comparison with non-carriers.

Conclusion

This study shows that carriers of germline mutations in a DDRP gene have an increased risk of developing (contralateral) breast cancer after radiotherapy; that is, over and above the risk associated with their carrier status. The increased risk indicates that knowledge of germline status of these DDRP genes at the time of breast cancer diagnosis may have important implications for the choice of treatment.
Literature
1.
go back to reference Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, Loman N, Olsson H, Johannsson O, Borg A, et al: Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet. 2003, 72: 1117-1130. 10.1086/375033.CrossRefPubMedPubMedCentral Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, Loman N, Olsson H, Johannsson O, Borg A, et al: Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet. 2003, 72: 1117-1130. 10.1086/375033.CrossRefPubMedPubMedCentral
2.
go back to reference Narod SA: Modifiers of risk of hereditary breast and ovarian cancer. Nat Rev Cancer. 2002, 2: 113-123. 10.1038/nrc726.CrossRefPubMed Narod SA: Modifiers of risk of hereditary breast and ovarian cancer. Nat Rev Cancer. 2002, 2: 113-123. 10.1038/nrc726.CrossRefPubMed
3.
go back to reference Narod SA, Foulkes WD: BRCA1 and BRCA2: 1994 and beyond. Nat Rev Cancer. 2004, 4: 665-676. 10.1038/nrc1431.CrossRefPubMed Narod SA, Foulkes WD: BRCA1 and BRCA2: 1994 and beyond. Nat Rev Cancer. 2004, 4: 665-676. 10.1038/nrc1431.CrossRefPubMed
4.
go back to reference Andrieu N, Easton DF, Chang-Claude J, Rookus MA, Brohet R, Cardis E, Antoniou AC, Wagner T, Simard J, Evans G, et al: Effect of chest X-rays on the risk of breast cancer among BRCA1/2 mutation carriers in the international BRCA1/2 carrier cohort study: a report from the EMBRACE, GENEPSO, GEO-HEBON, and IBCCS Collaborators' Group. J Clin Oncol. 2006, 24: 3361-3366. 10.1200/JCO.2005.03.3126.CrossRefPubMed Andrieu N, Easton DF, Chang-Claude J, Rookus MA, Brohet R, Cardis E, Antoniou AC, Wagner T, Simard J, Evans G, et al: Effect of chest X-rays on the risk of breast cancer among BRCA1/2 mutation carriers in the international BRCA1/2 carrier cohort study: a report from the EMBRACE, GENEPSO, GEO-HEBON, and IBCCS Collaborators' Group. J Clin Oncol. 2006, 24: 3361-3366. 10.1200/JCO.2005.03.3126.CrossRefPubMed
5.
go back to reference Dumitrescu RG, Cotarla I: Understanding breast cancer risk – where do we stand in 2005?. J Cell Mol Med. 2005, 9: 208-221. 10.1111/j.1582-4934.2005.tb00350.x.CrossRefPubMed Dumitrescu RG, Cotarla I: Understanding breast cancer risk – where do we stand in 2005?. J Cell Mol Med. 2005, 9: 208-221. 10.1111/j.1582-4934.2005.tb00350.x.CrossRefPubMed
6.
go back to reference Thompson D, Duedal S, Kirner J, McGuffog L, Last J, Reiman A, Byrd P, Taylor M, Easton DF: Cancer risks and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst. 2005, 97: 813-822.CrossRefPubMed Thompson D, Duedal S, Kirner J, McGuffog L, Last J, Reiman A, Byrd P, Taylor M, Easton DF: Cancer risks and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst. 2005, 97: 813-822.CrossRefPubMed
7.
go back to reference Broeks A, Urbanus JH, Floore AN, Dahler EC, Klijn JG, Rutgers EJ, Devilee P, Russell NS, van Leeuwen FE, van't Veer LJ: ATM-heterozygous germline mutations contribute to breast cancer- susceptibility. Am J Hum Genet. 2000, 66: 494-500. 10.1086/302746.CrossRefPubMedPubMedCentral Broeks A, Urbanus JH, Floore AN, Dahler EC, Klijn JG, Rutgers EJ, Devilee P, Russell NS, van Leeuwen FE, van't Veer LJ: ATM-heterozygous germline mutations contribute to breast cancer- susceptibility. Am J Hum Genet. 2000, 66: 494-500. 10.1086/302746.CrossRefPubMedPubMedCentral
8.
go back to reference Gutierrez-Enriquez S, Fernet M, Dork T, Bremer M, Lauge A, Stoppa-Lyonnet D, Moullan N, Angele S, Hall J: Functional consequences of ATM sequence variants for chromosomal radiosensitivity. Genes Chromosomes Cancer. 2004, 40: 109-119. 10.1002/gcc.20025.CrossRefPubMed Gutierrez-Enriquez S, Fernet M, Dork T, Bremer M, Lauge A, Stoppa-Lyonnet D, Moullan N, Angele S, Hall J: Functional consequences of ATM sequence variants for chromosomal radiosensitivity. Genes Chromosomes Cancer. 2004, 40: 109-119. 10.1002/gcc.20025.CrossRefPubMed
9.
go back to reference Smilenov LB, Brenner DJ, Hall EJ: Modest increased sensitivity to radiation oncogenesis in ATM heterozygous versus wild-type mammalian cells. Cancer Res. 2001, 61: 5710-5713.PubMed Smilenov LB, Brenner DJ, Hall EJ: Modest increased sensitivity to radiation oncogenesis in ATM heterozygous versus wild-type mammalian cells. Cancer Res. 2001, 61: 5710-5713.PubMed
10.
go back to reference Angele S, Romestaing P, Moullan N, Vuillaume M, Chapot B, Friesen M, Jongmans W, Cox DG, Pisani P, Gerard JP, Hall J: ATM haplotypes and cellular response to DNA damage: association with breast cancer risk and clinical radiosensitivity. Cancer Res. 2003, 63: 8717-8725.PubMed Angele S, Romestaing P, Moullan N, Vuillaume M, Chapot B, Friesen M, Jongmans W, Cox DG, Pisani P, Gerard JP, Hall J: ATM haplotypes and cellular response to DNA damage: association with breast cancer risk and clinical radiosensitivity. Cancer Res. 2003, 63: 8717-8725.PubMed
11.
go back to reference Vahteristo P, Bartkova J, Eerola H, Syrjakoski K, Ojala S, Kilpivaara O, Tamminen A, Kononen J, Aittomaki K, Heikkila P, et al: A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet. 2002, 71: 432-438. 10.1086/341943.CrossRefPubMedPubMedCentral Vahteristo P, Bartkova J, Eerola H, Syrjakoski K, Ojala S, Kilpivaara O, Tamminen A, Kononen J, Aittomaki K, Heikkila P, et al: A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet. 2002, 71: 432-438. 10.1086/341943.CrossRefPubMedPubMedCentral
12.
go back to reference Offit K, Pierce H, Kirchhoff T, Kolachana P, Rapaport B, Gregersen P, Johnson S, Yossepowitch O, Huang H, Satagopan J, et al: Frequency of CHEK2*1100delC in New York breast cancer cases and controls. BMC Med Genet. 2003, 4: 1-10.1186/1471-2350-4-1.CrossRefPubMedPubMedCentral Offit K, Pierce H, Kirchhoff T, Kolachana P, Rapaport B, Gregersen P, Johnson S, Yossepowitch O, Huang H, Satagopan J, et al: Frequency of CHEK2*1100delC in New York breast cancer cases and controls. BMC Med Genet. 2003, 4: 1-10.1186/1471-2350-4-1.CrossRefPubMedPubMedCentral
13.
go back to reference Sodha N, Bullock S, Taylor R, Mitchell G, Guertl-Lackner B, Williams RD, Bevan S, Bishop K, McGuire S, Houlston RS, Eeles RA: CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours. Br J Cancer. 2002, 87: 1445-1448. 10.1038/sj.bjc.6600637.CrossRefPubMedPubMedCentral Sodha N, Bullock S, Taylor R, Mitchell G, Guertl-Lackner B, Williams RD, Bevan S, Bishop K, McGuire S, Houlston RS, Eeles RA: CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours. Br J Cancer. 2002, 87: 1445-1448. 10.1038/sj.bjc.6600637.CrossRefPubMedPubMedCentral
14.
go back to reference Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, et al: Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002, 31: 55-59. 10.1038/ng879.CrossRefPubMed Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, et al: Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002, 31: 55-59. 10.1038/ng879.CrossRefPubMed
15.
go back to reference CHEK2 Breast Cancer Case-Control Consortium: CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet. 2004, 74: 1175-1182. 10.1086/421251.CrossRef CHEK2 Breast Cancer Case-Control Consortium: CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet. 2004, 74: 1175-1182. 10.1086/421251.CrossRef
16.
go back to reference Preston DL, Mattsson A, Holmberg E, Shore R, Hildreth NG, Boice JD: Radiation effects on breast cancer risk: a pooled analysis of eight cohorts. Radiat Res. 2002, 158: 220-235. 10.1667/0033-7587(2002)158[0220:REOBCR]2.0.CO;2.CrossRefPubMed Preston DL, Mattsson A, Holmberg E, Shore R, Hildreth NG, Boice JD: Radiation effects on breast cancer risk: a pooled analysis of eight cohorts. Radiat Res. 2002, 158: 220-235. 10.1667/0033-7587(2002)158[0220:REOBCR]2.0.CO;2.CrossRefPubMed
17.
go back to reference Scott D: Chromosomal radiosensitivity and low penetrance predisposition to cancer. Cytogenet Genome Res. 2004, 104: 365-370. 10.1159/000077517.CrossRefPubMed Scott D: Chromosomal radiosensitivity and low penetrance predisposition to cancer. Cytogenet Genome Res. 2004, 104: 365-370. 10.1159/000077517.CrossRefPubMed
18.
go back to reference Bennett LM: Breast cancer: genetic predisposition an exposure to radiation. Mol Carcinog. 1999, 26: 143-149. 10.1002/(SICI)1098-2744(199911)26:3<143::AID-MC2>3.0.CO;2-S.CrossRefPubMed Bennett LM: Breast cancer: genetic predisposition an exposure to radiation. Mol Carcinog. 1999, 26: 143-149. 10.1002/(SICI)1098-2744(199911)26:3<143::AID-MC2>3.0.CO;2-S.CrossRefPubMed
19.
go back to reference Boice JD, Monson RR: Breast cancer in women after repeated fluoroscopic examinations of the chest. J Natl Cancer Inst. 1977, 59: 823-832.PubMed Boice JD, Monson RR: Breast cancer in women after repeated fluoroscopic examinations of the chest. J Natl Cancer Inst. 1977, 59: 823-832.PubMed
20.
go back to reference Morin Doody M, Lonstein JE, Stovall M, Hacker DG, Luckyanov N, Land CE: Breast cancer mortality after diagnostic radiography: findings from the U.S. Scoliosis Cohort Study. Spine. 2000, 25: 2052-2063. 10.1097/00007632-200008150-00009.CrossRef Morin Doody M, Lonstein JE, Stovall M, Hacker DG, Luckyanov N, Land CE: Breast cancer mortality after diagnostic radiography: findings from the U.S. Scoliosis Cohort Study. Spine. 2000, 25: 2052-2063. 10.1097/00007632-200008150-00009.CrossRef
21.
go back to reference Bernstein JL, Teraoka SN, John EM, Andrulis IL, Knight JA, Lapinski R, Olson ER, Wolitzer AL, Seminara D, Whittemore AS, Concannon P: The CHEK2*1100delC allelic variant and risk of breast cancer: screening results from the Breast Cancer Family Registry. Cancer Epidemiol Biomarkers Prev. 2006, 15: 348-352. 10.1158/1055-9965.EPI-05-0557.CrossRefPubMed Bernstein JL, Teraoka SN, John EM, Andrulis IL, Knight JA, Lapinski R, Olson ER, Wolitzer AL, Seminara D, Whittemore AS, Concannon P: The CHEK2*1100delC allelic variant and risk of breast cancer: screening results from the Breast Cancer Family Registry. Cancer Epidemiol Biomarkers Prev. 2006, 15: 348-352. 10.1158/1055-9965.EPI-05-0557.CrossRefPubMed
22.
go back to reference Harvey EB, Brinton LA: Second cancer following cancer of the breast in Conneticut, 1935–1982. Natl Cancer Inst Monogr. 1985, 68: 99-112.PubMed Harvey EB, Brinton LA: Second cancer following cancer of the breast in Conneticut, 1935–1982. Natl Cancer Inst Monogr. 1985, 68: 99-112.PubMed
23.
go back to reference Boice JD, Harvey EB, Blettner M, Stovall M, Flannery JT: Cancer in the contralateral breast after radiotherapy for breast cancer. N Engl J Med. 1992, 326: 781-785.CrossRefPubMed Boice JD, Harvey EB, Blettner M, Stovall M, Flannery JT: Cancer in the contralateral breast after radiotherapy for breast cancer. N Engl J Med. 1992, 326: 781-785.CrossRefPubMed
24.
go back to reference Roychoudhuri R, Evans H, Robinson D, Moller H: Radiation-induced malignancies following radiotherapy for breast cancer. Br J Cancer. 2004, 91: 868-872.PubMedPubMedCentral Roychoudhuri R, Evans H, Robinson D, Moller H: Radiation-induced malignancies following radiotherapy for breast cancer. Br J Cancer. 2004, 91: 868-872.PubMedPubMedCentral
25.
go back to reference Haffty BG: Radiation therapy and the risk of contralateral breast cancer. Int J Radiat Oncol Biol Phys. 2003, 56: 920-921. 10.1016/S0360-3016(03)00204-9.CrossRefPubMed Haffty BG: Radiation therapy and the risk of contralateral breast cancer. Int J Radiat Oncol Biol Phys. 2003, 56: 920-921. 10.1016/S0360-3016(03)00204-9.CrossRefPubMed
26.
go back to reference Rothman KJ, Greenland S: Case-control studies. Modern Epidemiology. Edited by: Rothman KJ, Greenland S. 1998, Philadelphia: Lippincott-Raven, 615-617. Rothman KJ, Greenland S: Case-control studies. Modern Epidemiology. Edited by: Rothman KJ, Greenland S. 1998, Philadelphia: Lippincott-Raven, 615-617.
27.
go back to reference Ursin G, Henderson BE, Haile RW, Pike MC, Zhou N, Diep A, Bernstein L: Does oral contraceptive use increase the risk of breast cancer in women with BRCA1/BRCA2 mutations more than in other women?. Cancer Res. 1997, 57: 3678-3681.PubMed Ursin G, Henderson BE, Haile RW, Pike MC, Zhou N, Diep A, Bernstein L: Does oral contraceptive use increase the risk of breast cancer in women with BRCA1/BRCA2 mutations more than in other women?. Cancer Res. 1997, 57: 3678-3681.PubMed
28.
go back to reference Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: a Laboratory Manual. 1989, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, 2 Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: a Laboratory Manual. 1989, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, 2
30.
go back to reference Breslow NE, Day NE: Statistical methods in cancer research. The analysis of case-control studies. IARC Sci Publ. 1980, (32): 5-338. Breslow NE, Day NE: Statistical methods in cancer research. The analysis of case-control studies. IARC Sci Publ. 1980, (32): 5-338.
31.
go back to reference Broeks A, Braaf LM, Huseinovic A, Schmidt MK, Russell NS, Van Leeuwen FE, Hogervorst FBL, van't Veer LJ: The spectrum of ATMmissense variants and their contribution to contralateral breast cancer. Breast Cancer Res Treat. 2007, Mar 28, Broeks A, Braaf LM, Huseinovic A, Schmidt MK, Russell NS, Van Leeuwen FE, Hogervorst FBL, van't Veer LJ: The spectrum of ATMmissense variants and their contribution to contralateral breast cancer. Breast Cancer Res Treat. 2007, Mar 28,
32.
go back to reference Boice JD, Land CE, Preston DL: Ionizing radiation. Cancer Epidemiology and Prevention. Edited by: Schottenfield D, Fraumeni JF Jr. 1996, 319-341. New York: Oxford University Press Boice JD, Land CE, Preston DL: Ionizing radiation. Cancer Epidemiology and Prevention. Edited by: Schottenfield D, Fraumeni JF Jr. 1996, 319-341. New York: Oxford University Press
33.
go back to reference Land CE, Tokunaga M, Koyama K, Soda M, Preston DL, Nishimori I, Tokuoka S: Incidence of female breast cancer among atomic bomb survivors, Hiroshima and Nagasaki, 1950–1990. Radiat Res. 2003, 160: 707-717. 10.1667/RR3082.CrossRefPubMed Land CE, Tokunaga M, Koyama K, Soda M, Preston DL, Nishimori I, Tokuoka S: Incidence of female breast cancer among atomic bomb survivors, Hiroshima and Nagasaki, 1950–1990. Radiat Res. 2003, 160: 707-717. 10.1667/RR3082.CrossRefPubMed
34.
go back to reference Howe GR, McLaughlin J: Breast cancer mortality between 1950 and 1987 after exposure to fractionated moderate-dose-rate ionizing radiation in the Canadian fluoroscopy cohort study and a comparison with breast cancer mortality in the atomic bomb survivors study. Radiat Res. 1996, 145: 694-707. 10.2307/3579360.CrossRefPubMed Howe GR, McLaughlin J: Breast cancer mortality between 1950 and 1987 after exposure to fractionated moderate-dose-rate ionizing radiation in the Canadian fluoroscopy cohort study and a comparison with breast cancer mortality in the atomic bomb survivors study. Radiat Res. 1996, 145: 694-707. 10.2307/3579360.CrossRefPubMed
35.
go back to reference Broeks A, de Witte L, Nooijen A, Huseinovic A, Klijn JG, van Leeuwen FE, Russell NS, van't Veer LJ: Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers. Breast Cancer Res Treat. 2004, 83: 91-93. 10.1023/B:BREA.0000010697.49896.03.CrossRefPubMed Broeks A, de Witte L, Nooijen A, Huseinovic A, Klijn JG, van Leeuwen FE, Russell NS, van't Veer LJ: Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers. Breast Cancer Res Treat. 2004, 83: 91-93. 10.1023/B:BREA.0000010697.49896.03.CrossRefPubMed
36.
go back to reference Metcalfe K, Lynch HT, Ghadirian P, Tung N, Olivotto I, Warner E, Olopade OI, Eisen A, Weber B, McLennan J, et al: Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers. J Clin Oncol. 2004, 22: 2328-2335. 10.1200/JCO.2004.04.033.CrossRefPubMed Metcalfe K, Lynch HT, Ghadirian P, Tung N, Olivotto I, Warner E, Olopade OI, Eisen A, Weber B, McLennan J, et al: Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers. J Clin Oncol. 2004, 22: 2328-2335. 10.1200/JCO.2004.04.033.CrossRefPubMed
37.
go back to reference Verhoog LC, Brekelmans CT, Seynaeve C, van den Bosch LM, Dahmen G, van Geel AN, Tilanus-Linthorst MM, Bartels CC, Wagner A, van den Ouweland A, et al: Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1. Lancet. 1998, 351: 316-321. 10.1016/S0140-6736(97)07065-7.CrossRefPubMed Verhoog LC, Brekelmans CT, Seynaeve C, van den Bosch LM, Dahmen G, van Geel AN, Tilanus-Linthorst MM, Bartels CC, Wagner A, van den Ouweland A, et al: Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1. Lancet. 1998, 351: 316-321. 10.1016/S0140-6736(97)07065-7.CrossRefPubMed
38.
go back to reference Verhoog LC, Brekelmans CT, Seynaeve C, Meijers-Heijboer EJ, Klijn JG: Contralateral breast cancer risk is influenced by the age at onset in BRCA1-associated breast cancer. Br J Cancer. 2000, 83: 384-386. 10.1054/bjoc.2000.1239.CrossRefPubMedPubMedCentral Verhoog LC, Brekelmans CT, Seynaeve C, Meijers-Heijboer EJ, Klijn JG: Contralateral breast cancer risk is influenced by the age at onset in BRCA1-associated breast cancer. Br J Cancer. 2000, 83: 384-386. 10.1054/bjoc.2000.1239.CrossRefPubMedPubMedCentral
39.
go back to reference Schmidt MK, Tollenaar RA, de Kemp SR, Broeks A, Cornelisse CJ, Smit VT, Peterse JL, van Leeuwen FE, Van 't Veer LJ: Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation. J Clin Oncol. 2007, 25: 64-9. 10.1200/JCO.2006.06.3024.CrossRefPubMed Schmidt MK, Tollenaar RA, de Kemp SR, Broeks A, Cornelisse CJ, Smit VT, Peterse JL, van Leeuwen FE, Van 't Veer LJ: Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation. J Clin Oncol. 2007, 25: 64-9. 10.1200/JCO.2006.06.3024.CrossRefPubMed
40.
go back to reference Ronckers CM, Erdmann CA, Land CE: Radiation and breast cancer: a review of current evidence. Breast Cancer Res. 2005, 7: 21-32. 10.1186/bcr970.CrossRefPubMed Ronckers CM, Erdmann CA, Land CE: Radiation and breast cancer: a review of current evidence. Breast Cancer Res. 2005, 7: 21-32. 10.1186/bcr970.CrossRefPubMed
41.
go back to reference Gatti RA, Tward A, Concannon P: Cancer risk in ATM heterozygotes: a model of phenotypic and mechanistic differences between missense and truncating mutations. Mol Genet Metab. 1999, 68: 419-423. 10.1006/mgme.1999.2942.CrossRefPubMed Gatti RA, Tward A, Concannon P: Cancer risk in ATM heterozygotes: a model of phenotypic and mechanistic differences between missense and truncating mutations. Mol Genet Metab. 1999, 68: 419-423. 10.1006/mgme.1999.2942.CrossRefPubMed
42.
go back to reference Thorstenson YR, Roxas A, Kroiss R, Jenkins MA, Yu KM, Bachrich T, Muhr D, Wayne TL, Chu G, Davis RW, et al: Contributions of ATM mutations to familial breast and ovarian cancer. Cancer Res. 2003, 63: 3325-3333.PubMed Thorstenson YR, Roxas A, Kroiss R, Jenkins MA, Yu KM, Bachrich T, Muhr D, Wayne TL, Chu G, Davis RW, et al: Contributions of ATM mutations to familial breast and ovarian cancer. Cancer Res. 2003, 63: 3325-3333.PubMed
43.
go back to reference Scott SP, Bendix R, Chen P, Clark R, Dork T, Lavin MF: Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer. Proc Natl Acad Sci USA. 2002, 99: 925-930. 10.1073/pnas.012329699.CrossRefPubMedPubMedCentral Scott SP, Bendix R, Chen P, Clark R, Dork T, Lavin MF: Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer. Proc Natl Acad Sci USA. 2002, 99: 925-930. 10.1073/pnas.012329699.CrossRefPubMedPubMedCentral
44.
go back to reference Fu YP, Yu JC, Cheng TC, Lou MA, Hsu GC, Wu CY, Chen ST, Wu HS, Wu PE, Shen CY: Breast cancer risk associated with genotypic polymorphism of the nonhomologous end-joining genes: a multigenic study on cancer susceptibility. Cancer Res. 2003, 63: 2440-2446.PubMed Fu YP, Yu JC, Cheng TC, Lou MA, Hsu GC, Wu CY, Chen ST, Wu HS, Wu PE, Shen CY: Breast cancer risk associated with genotypic polymorphism of the nonhomologous end-joining genes: a multigenic study on cancer susceptibility. Cancer Res. 2003, 63: 2440-2446.PubMed
45.
go back to reference Bernstein JL, Langholz B, Haile RW, Bernstein L, Thomas DC, Stovall M, Malone KE, Lynch CF, Olsen JH, Anton-Culver H, et al: Study design: evaluating gene-environment interactions in the etiology of breast cancer – the WECARE study. Breast Cancer Res. 2004, 6: R199-R214. 10.1186/bcr771.CrossRefPubMedPubMedCentral Bernstein JL, Langholz B, Haile RW, Bernstein L, Thomas DC, Stovall M, Malone KE, Lynch CF, Olsen JH, Anton-Culver H, et al: Study design: evaluating gene-environment interactions in the etiology of breast cancer – the WECARE study. Breast Cancer Res. 2004, 6: R199-R214. 10.1186/bcr771.CrossRefPubMedPubMedCentral
Metadata
Title
Identification of women with an increased risk of developing radiation-induced breast cancer: a case only study
Authors
Annegien Broeks
Linde M Braaf
Angelina Huseinovic
Anke Nooijen
Jos Urbanus
Frans BL Hogervorst
Marjanka K Schmidt
Jan GM Klijn
Nicola S Russell
Flora E Van Leeuwen
Laura J Van 't Veer
Publication date
01-12-2007
Publisher
BioMed Central
Published in
Breast Cancer Research / Issue 2/2007
Electronic ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr1668

Other articles of this Issue 2/2007

Breast Cancer Research 2/2007 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine