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BCL11A is a triple-negative breast cancer gene with critical functions in stem and progenitor cells.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Khaled, Walid T 
Choon Lee, Song 
Stingl, John 
Chen, Xiongfeng 
Raza Ali, H 

Abstract

Triple-negative breast cancer (TNBC) has poor prognostic outcome compared with other types of breast cancer. The molecular and cellular mechanisms underlying TNBC pathology are not fully understood. Here, we report that the transcription factor BCL11A is overexpressed in TNBC including basal-like breast cancer (BLBC) and that its genomic locus is amplified in up to 38% of BLBC tumours. Exogenous BCL11A overexpression promotes tumour formation, whereas its knockdown in TNBC cell lines suppresses their tumourigenic potential in xenograft models. In the DMBA-induced tumour model, Bcl11a deletion substantially decreases tumour formation, even in p53-null cells and inactivation of Bcl11a in established tumours causes their regression. At the cellular level, Bcl11a deletion causes a reduction in the number of mammary epithelial stem and progenitor cells. Thus, BCL11A has an important role in TNBC and normal mammary epithelial cells. This study highlights the importance of further investigation of BCL11A in TNBC-targeted therapies.

Description

Keywords

9,10-Dimethyl-1,2-benzanthracene, Animals, Carrier Proteins, Cell Line, Tumor, Cell Proliferation, Cell Survival, DNA-Binding Proteins, Female, Gene Expression Regulation, Neoplastic, Humans, Immunohistochemistry, Mammary Glands, Animal, Mice, Neoplasm Transplantation, Nuclear Proteins, Oligonucleotide Array Sequence Analysis, Prognosis, Repressor Proteins, Stem Cells, Triple Negative Breast Neoplasms

Journal Title

Nat Commun

Conference Name

Journal ISSN

2041-1723
2041-1723

Volume Title

6

Publisher

Springer Science and Business Media LLC
Sponsorship
Cancer Research UK (17348)