The Proliferative and Apoptotic Landscape of Basal-like Breast Cancer

被引:28
作者
Alexandrou, Sarah [1 ]
George, Sandra Marie [1 ]
Ormandy, Christopher John [1 ,2 ]
Lim, Elgene [1 ,2 ]
Oakes, Samantha Richelle [1 ,2 ]
Caldon, C. Elizabeth [1 ,2 ]
机构
[1] Garvan Inst Med Res, Kinghorn Canc Ctr, Sydney, NSW 2010, Australia
[2] UNSW Sydney, St Vincents Clin Sch, Fac Med, Sydney, NSW 2052, Australia
关键词
basal-like breast cancer; BLBC; triple-negative breast cancer; TNBC; targeted therapies; cell cycle; apoptosis; ALPHA-B-CRYSTALLIN; CHRONIC LYMPHOCYTIC-LEUKEMIA; CYCLIN-DEPENDENT KINASES; DNA-DAMAGE RESPONSE; BCL-2 PROTEIN FAMILY; THERAPEUTIC TARGET; NEOADJUVANT CHEMOTHERAPY; RETINOBLASTOMA PROTEIN; ANTITUMOR-ACTIVITY; CELL-LINES;
D O I
10.3390/ijms20030667
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Basal-like breast cancer (BLBC) is an aggressive molecular subtype that represents up to 15% of breast cancers. It occurs in younger patients, and typically shows rapid development of locoregional and distant metastasis, resulting in a relatively high mortality rate. Its defining features are that it is positive for basal cytokeratins and, epidermal growth factor receptor and/or c-Kit. Problematically, it is typically negative for the estrogen receptor and human epidermal growth factor receptor 2 (HER2), which means that it is unsuitable for either hormone therapy or targeted HER2 therapy. As a result, there are few therapeutic options for BLBC, and a major priority is to define molecular subgroups of BLBC that could be targeted therapeutically. In this review, we focus on the highly proliferative and anti-apoptotic phenotype of BLBC with the goal of defining potential therapeutic avenues, which could take advantage of these aspects of tumor development.
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页数:30
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