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Volumn 49, Issue 8, 2013, Pages 1993-1999

Excess breast cancer risk in first degree relatives of CHEK2* 1100delC positive familial breast cancer cases

Author keywords

Breast cancer; Cancer incidence; CHEK2; CHEK2*1100delC; Familial; Relatives

Indexed keywords

CHECKPOINT KINASE 2;

EID: 84876683067     PISSN: 09598049     EISSN: 18790852     Source Type: Journal    
DOI: 10.1016/j.ejca.2013.01.009     Document Type: Article
Times cited : (21)

References (22)
  • 1
    • 18544389716 scopus 로고    scopus 로고
    • Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations
    • H. Meijers-Heijboer, A. van den Ouweland, and J. Klijn Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations Nat Genet 31 2002 55 59
    • (2002) Nat Genet , vol.31 , pp. 55-59
    • Meijers-Heijboer, H.1    Van Den Ouweland, A.2    Klijn, J.3
  • 2
    • 36448973875 scopus 로고    scopus 로고
    • CHK2 kinase: Cancer susceptibility and cancer therapy-two sides of the same coin?
    • L. Antoni, N. Sodha, I. Collins, and M.D. Garrett CHK2 kinase: cancer susceptibility and cancer therapy-two sides of the same coin? Nat Rev Cancer 7 2007 925 936
    • (2007) Nat Rev Cancer , vol.7 , pp. 925-936
    • Antoni, L.1    Sodha, N.2    Collins, I.3    Garrett, M.D.4
  • 3
    • 3042582651 scopus 로고    scopus 로고
    • CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9065 controls from 10 studies
    • The CHEK2 breast cancer case-control consortium
    • The CHEK2 breast cancer case-control consortium CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9065 controls from 10 studies Am J Hum Genet 74 2004 1175 1182
    • (2004) Am J Hum Genet , vol.74 , pp. 1175-1182
  • 4
    • 77954579781 scopus 로고    scopus 로고
    • Testing for CHEK2 in the cancer genetics clinic: Ready for prime time?
    • S.A. Narod Testing for CHEK2 in the cancer genetics clinic: ready for prime time? Clin Genet 78 2010 1 7
    • (2010) Clin Genet , vol.78 , pp. 1-7
    • Narod, S.A.1
  • 5
    • 58349121873 scopus 로고    scopus 로고
    • Family history, genetic testing, and clinical risk prediction: Pooled analysis of CHEK2*1100delC in 1828 bilateral breast cancers and 7030 controls
    • O. Fletcher, N. Johnson, and I. Dos Santos Silva Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2*1100delC in 1828 bilateral breast cancers and 7030 controls Cancer Epidemiol Biomarkers Prev 18 2009 230 234
    • (2009) Cancer Epidemiol Biomarkers Prev , vol.18 , pp. 230-234
    • Fletcher, O.1    Johnson, N.2    Dos Santos Silva, I.3
  • 6
    • 39149141409 scopus 로고    scopus 로고
    • CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: Meta-analyses of 26,000 patient cases and 27,000 controls
    • M. Weischer, S.E. Bojesen, C. Ellervik, A. Tybjaerg-Hansen, and D.G. Nordestgaard CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls J Clin Oncol 26 2008 542 548
    • (2008) J Clin Oncol , vol.26 , pp. 542-548
    • Weischer, M.1    Bojesen, S.E.2    Ellervik, C.3    Tybjaerg-Hansen, A.4    Nordestgaard, D.G.5
  • 7
    • 80053594059 scopus 로고    scopus 로고
    • Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer
    • C. Cybulski, D. Wokolorczyk, and A. Jakubowska Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer J Clin Oncol 29 2011 3747 3752
    • (2011) J Clin Oncol , vol.29 , pp. 3747-3752
    • Cybulski, C.1    Wokolorczyk, D.2    Jakubowska, A.3
  • 9
    • 0347626108 scopus 로고    scopus 로고
    • The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/2 multiple-case families
    • R.A. Oldenburg, K. Kroeze-Jansema, and J. Kraan The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/2 multiple-case families Cancer Res 63 2003 8153 8157
    • (2003) Cancer Res , vol.63 , pp. 8153-8157
    • Oldenburg, R.A.1    Kroeze-Jansema, K.2    Kraan, J.3
  • 10
    • 0035960431 scopus 로고    scopus 로고
    • Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease
    • Collaborative Group on Hormonal Factors in Breast Cancer
    • Collaborative Group on Hormonal Factors in Breast Cancer Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58 209 women with breast cancer and 101 986 women without the disease Lancet 358 2001 1389 1399
    • (2001) Lancet , vol.358 , pp. 1389-1399
  • 11
    • 39149122546 scopus 로고    scopus 로고
    • Time to check CHEK2 in families with breast cancer?
    • K. Offit, and J.E. Garber Time to check CHEK2 in families with breast cancer? J Clin Oncol 26 2008 519 520
    • (2008) J Clin Oncol , vol.26 , pp. 519-520
    • Offit, K.1    Garber, J.E.2
  • 12
    • 77954601802 scopus 로고    scopus 로고
    • CHEK2, breast cancer, and the understanding of clinical utility
    • M. Robson CHEK2, breast cancer, and the understanding of clinical utility Clin Genet 78 2010 8 10
    • (2010) Clin Genet , vol.78 , pp. 8-10
    • Robson, M.1
  • 13
    • 84856014217 scopus 로고    scopus 로고
    • CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women
    • M.A. Adank, M.A. Jonker, and I. Kluijt CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women J Med Genet 48 2011 860 863
    • (2011) J Med Genet , vol.48 , pp. 860-863
    • Adank, M.A.1    Jonker, M.A.2    Kluijt, I.3
  • 14
    • 65549155934 scopus 로고    scopus 로고
    • Cancer risks in first-degree relatives of CHEK2 mutation carriers: Effects of mutation type and cancer site in proband
    • J. Gronwald, C. Cybulski, and W. Piesiak Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband Br J Cancer 100 2009 1508 1512
    • (2009) Br J Cancer , vol.100 , pp. 1508-1512
    • Gronwald, J.1    Cybulski, C.2    Piesiak, W.3
  • 15
    • 51049084415 scopus 로고    scopus 로고
    • CHEK2 1100delC is a susceptibility allele for HNPCC-related colorectal cancer
    • M. Wasielewski, H. Vasen, and J. Wijnen CHEK2 1100delC is a susceptibility allele for HNPCC-related colorectal cancer Clin Cancer Res 14 2008 4989 4994
    • (2008) Clin Cancer Res , vol.14 , pp. 4989-4994
    • Wasielewski, M.1    Vasen, H.2    Wijnen, J.3
  • 16
    • 80755186927 scopus 로고    scopus 로고
    • Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility
    • H.P. Xiang, X.P. Geng, W.W. Ge, and H. Li Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility Eur J Cancer 47 2011 2546 2551
    • (2011) Eur J Cancer , vol.47 , pp. 2546-2551
    • Xiang, H.P.1    Geng, X.P.2    Ge, W.W.3    Li, H.4
  • 17
    • 84859105556 scopus 로고    scopus 로고
    • Risk of breast cancer in families of multiple affected women and men
    • M. Bevier, K. Sundquist, and K. Hemminki Risk of breast cancer in families of multiple affected women and men Breast Cancer Res Treat 132 2011 723 728
    • (2011) Breast Cancer Res Treat , vol.132 , pp. 723-728
    • Bevier, M.1    Sundquist, K.2    Hemminki, K.3
  • 18
    • 27544515629 scopus 로고    scopus 로고
    • Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: A familial study
    • N. Johnson, O. Fletcher, C. Naceur-Lombardelli, I. Dos Santos Silva, A. Ashworth, and J. Peto Interaction between CHEK2*1100delC and other low-penetrance breast-cancer susceptibility genes: a familial study Lancet 366 2005 1554 1557
    • (2005) Lancet , vol.366 , pp. 1554-1557
    • Johnson, N.1    Fletcher, O.2    Naceur-Lombardelli, C.3    Dos Santos Silva, I.4    Ashworth, A.5    Peto, J.6
  • 19
    • 0942279575 scopus 로고    scopus 로고
    • Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers
    • A. Broeks, L. de Witte, and A. Nooijen Excess risk for contralateral breast cancer in CHEK2*1100delC germline mutation carriers Breast Cancer Res Treat 83 2004 91 93
    • (2004) Breast Cancer Res Treat , vol.83 , pp. 91-93
    • Broeks, A.1    De Witte, L.2    Nooijen, A.3
  • 20
    • 39449090355 scopus 로고    scopus 로고
    • Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study
    • L. Mellemkjaer, C. Dahl, and J.H. Olsen Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study Br J Cancer 98 2008 728 733
    • (2008) Br J Cancer , vol.98 , pp. 728-733
    • Mellemkjaer, L.1    Dahl, C.2    Olsen, J.H.3
  • 21
    • 77956097177 scopus 로고    scopus 로고
    • BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries
    • D.G. Evans, M. Ahmed, S. Bayliss, E. Howard, F. Lalloo, and A. Wallace BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries J Med Genet 47 2010 561 566
    • (2010) J Med Genet , vol.47 , pp. 561-566
    • Evans, D.G.1    Ahmed, M.2    Bayliss, S.3    Howard, E.4    Lalloo, F.5    Wallace, A.6
  • 22
    • 33846012859 scopus 로고    scopus 로고
    • A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers
    • D. Thompson, S. Seal, and M. Schutte A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers Cancer Epidemiol Biomarkers Prev 15 2006 2542 2545
    • (2006) Cancer Epidemiol Biomarkers Prev , vol.15 , pp. 2542-2545
    • Thompson, D.1    Seal, S.2    Schutte, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.