The basal phenotype of BRCA1-related breast cancer - Past, present and future

被引:44
作者
Tischkowitz, MD
Foulkes, WD
机构
[1] McGill Univ, Canc Prevent Ctr, Sir Mortimer B Davis Jewish Hosp, Montreal, PQ, Canada
[2] McGill Univ, Dept Oncol, Program Canc Genet, Montreal, PQ, Canada
[3] McGill Univ, Dept Human Genet, Program Canc Genet, Montreal, PQ, Canada
关键词
breast cancer; BRCA1; basal phenotype; breast stem cells;
D O I
10.4161/cc.5.9.2713
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many BRCA1-related tumors have a distinct histological characteristics which together have been called "basal-like." Typically such tumors are ER-, HER2- and express cytokeratin 5/6, cytokeratin 8/18, EGFR and vimentin. These characteristics can be used to predict which breast cancers are most likely to be associated with germline BRCA1 mutations which has important implications for breast pathologists. Moreover, BRCA1-related breast cancers generally have a poorer prognosis which may paradoxically be more pronounced in node negative cancers. This may relate in part to a different pattern of metastatic spread with in increased frequency of brain and lung metastases in BRCA1 carriers. Conversely, BRCA1-related tumors may respond better to neoadjuvant chemotherapy and their characteristic molecular signature may provide opportunities to develop specific molecular targeted therapies akin to traztuzumab in HER2+ cancers. Finally, many of the phenotypic features of BRCA1-related tumors might also be found in putative breast stem cells and therefore characterization of the BRCA1 breast cancer phenotype will improve our understanding of sporadic breast carcinogenesis.
引用
收藏
页码:963 / 967
页数:5
相关论文
共 70 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   Spectrum of breast cancer metastasis in BRCA1 mutation carriers:: highly increased incidence of brain metastases [J].
Albiges, L ;
André, F ;
Balleyguier, C ;
Gomez-Abuin, G ;
Chompret, A ;
Delaloge, S .
ANNALS OF ONCOLOGY, 2005, 16 (11) :1846-U3
[3]   Survival in early-onset BRCA1 breast-cancer patients [J].
Ansquer, Y ;
Gautier, C ;
Fourquet, A ;
Asselain, B ;
Stoppa-Lyonnet, D .
LANCET, 1998, 352 (9127) :541-541
[4]   Placental cadherin and the basal epithelial phenotype of BRCA1-related breast cancer [J].
Arnes, JB ;
Brunet, JS ;
Stefansson, I ;
Bégin, LR ;
Wong, N ;
Chappuis, PO ;
Akslen, LA ;
Foulkes, WD .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :4003-4011
[5]   Tyrosine kinase inhibitors: Why does the current process of clinical development not apply to them? [J].
Arteaga, CL ;
Baselga, J .
CANCER CELL, 2004, 5 (06) :525-531
[6]   BRCA1 regulates gene expression for orderly mitotic progression [J].
Bae, I ;
Rih, JK ;
Kim, HJ ;
Kang, HJ ;
Haddad, B ;
Kirilyuk, A ;
Fan, SJ ;
Avantaggiati, ML ;
Rosen, EM .
CELL CYCLE, 2005, 4 (11) :1641-1666
[7]   Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G ;
La Vecchia, C ;
Magnusson, C ;
Miller, T ;
Peterson, B ;
Pike, M ;
Thomas, D ;
van Leeuwen, F .
LANCET, 2002, 360 (9328) :187-195
[8]   Common adult stem cells in the human breast give rise to glandular and myoepithelial cell lineages:: A new cell biological concept [J].
Böcker, W ;
Moll, R ;
Poremba, C ;
Holland, R ;
van Diest, PJ ;
Dervan, P ;
Bürger, H ;
Wai, D ;
Diallo, RI ;
Brandt, B ;
Herbst, H ;
Schmidt, A ;
Lerch, MM ;
Buchwallow, IB .
LABORATORY INVESTIGATION, 2002, 82 (06) :737-745
[9]   Opinion - Migrating cancer stem cells - an integrated concept of malignant tumour progression [J].
Brabletz, T ;
Jung, A ;
Spaderna, S ;
Hlubek, F ;
Kirchner, T .
NATURE REVIEWS CANCER, 2005, 5 (09) :744-749
[10]   Assessing the link between BACH1 and BRCA1 in the FA pathway [J].
Cantor, SB ;
Andreassen, PR .
CELL CYCLE, 2006, 5 (02) :164-167