CHEK2 mutation and hereditary breast cancer

被引:14
作者
Narod, Steven A. [1 ]
Lynch, Henry T.
机构
[1] Ctr Res Womens Hlth, Toronto, ON, Canada
[2] Creighton Univ, Sch Med, Omaha, NE USA
关键词
TUMOR CHARACTERISTICS; CHEK2-ASTERISK-1100DELC; 1100DELC; FAMILIES; ALLELE; BRCA1; RISK;
D O I
10.1200/JCO.2006.08.8229
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
引用
收藏
页码:6 / 7
页数:2
相关论文
共 11 条
[1]
CYBULSKI C, BREAST CANC RES TREA
[2]
CHEK2-positive breast cancers in young Polish women [J].
Cybulski, Cezary ;
Gorski, Bohdan ;
Huzarski, Tomasz ;
Byrski, Tomasz ;
Gronwald, Jacek ;
Debniak, Tadeusz ;
Wokolorczyk, Dominika ;
Jakubowska, Anna ;
Kowalska, Elzbieta ;
Oszurek, Oleg ;
Narod, Steven A. ;
Lubinski, Jan .
CLINICAL CANCER RESEARCH, 2006, 12 (16) :4832-4835
[3]
Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families:: functional analysis in heterozygous individuals [J].
Jekimovs, CR ;
Chen, X ;
Arnold, J ;
Gatei, M ;
Richard, DJ ;
Spurdle, AB ;
Khanna, KK ;
Chenevix-Trench, G .
BRITISH JOURNAL OF CANCER, 2005, 92 (04) :784-790
[4]
Correlation of CHEK2 protein expression and c.1100delC mutation status with tumor characteristics among unselected breast cancer patients [J].
Kilpivaara, O ;
Bartkova, J ;
Eerola, A ;
Syrjäkoski, K ;
Vahteristo, P ;
Lukas, J ;
Blomqvist, C ;
Holli, K ;
Heikkilä, P ;
Sauter, G ;
Niemi, OPKI ;
Bartek, J ;
Nevanlinna, H .
INTERNATIONAL JOURNAL OF CANCER, 2005, 113 (04) :575-580
[5]
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations [J].
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 ;
Elstrodt, F ;
van Duijn, C ;
Bartels, C ;
Meijers, C ;
Schutte, M ;
McGuffog, L ;
Thompson, D ;
Easton, DF ;
Sodha, N ;
Seal, S ;
Barfoot, R ;
Mangion, J ;
Chang-Claude, J ;
Eccles, D ;
Eeles, R ;
Evans, DG ;
Houlston, R ;
Murday, V ;
Narod, S ;
Peretz, T ;
Peto, J ;
Phelan, C ;
Zhang, HX ;
Szabo, C ;
Devilee, P ;
Goldgar, D ;
Futreal, PA ;
Nathanson, KL ;
Weber, BL ;
Rahman, N ;
Stratton, MR .
NATURE GENETICS, 2002, 31 (01) :55-59
[6]
Offit K., 2003, BMC MED GENET, V4, P1, DOI DOI 10.1186/1471-2350-4-1
[7]
The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population [J].
Osorio, A ;
Rodríguez-López, R ;
Díez, O ;
de la Hoya, M ;
Martínez, JI ;
Vega, A ;
Esteban-Cardeñosa, E ;
Alonso, C ;
Caldés, T ;
Benítez, J .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (01) :54-56
[8]
German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer [J].
Rashid, MU ;
Jakubowska, A ;
Justenhoven, C ;
Harth, V ;
Pesch, B ;
Baisch, C ;
Pierl, CB ;
Brüning, T ;
Ko, Y ;
Benner, A ;
Wichmann, HE ;
Rauch, H ;
Hamann, U .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (18) :2896-2903
[9]
Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation [J].
Schmidt, Marjanka K. ;
Tollenaar, Rob A. E. M. ;
de Kemp, Sanne R. ;
Broeks, Annegien ;
Cornelisse, Cees J. ;
Smit, Vincent T. H. B. M. ;
Peterse, Johannes L. ;
van Leeuwen, Flora E. ;
Van't Veer, Laura J. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (01) :64-69
[10]
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer [J].
Walsh, T ;
Casadei, S ;
Coats, KH ;
Swisher, E ;
Stray, SM ;
Higgins, J ;
Roach, KC ;
Mandell, J ;
Lee, MK ;
Ciernikova, S ;
Foretova, L ;
Soucek, P ;
King, MC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (12) :1379-1388