Oestrogen increases the activity of oestrogen receptor-negative breast cancer stem cells through paracrine EGFR and Notch signalling

IntroductionAlthough oestrogen is essential for the development of the normal breast, adult mammary stem cells are known to be oestrogen receptor alpha (ER) negative and rely on paracrine signals in the mammary epithelium for mediation of developmental cues. However, little is known about how systemic oestrogen regulates breast cancer stem cell (CSC) activity.

Methods: Here, we tested the effects of oestrogen on CSC activity in vitro and in vivo and investigated which paracrine signalling pathways locally mediate oestrogen effects.

Results: CSC-enriched populations (ESA+CD44+CD24low) sorted from ER positive patient-derived and established cell lines have low or absent ER expression.

However, oestrogen stimulated CSC activity demonstrated by increased mammosphere and holoclone formation in vitro and tumour formation in vivo. This effect was abrogated by the anti-oestrogen tamoxifen or ER siRNA.

These data suggest that the oestrogen response is mediated through paracrine signalling from non-CSCs to CSCs. We have therefore investigated both epidermal growth factor (EGF) and Notch receptor signals down-stream of oestrogen.

We demonstrate that gefitinib (EGFR inhibitor) and gamma secretase inhibitors (Notch inhibitor) block oestrogen-induced CSC activity in vitro and in vivo but GSIs more efficiently reduce CSC frequency.

Conclusions: These data establish that EGF and Notch receptor signalling pathways operate downstream of oestrogen in the regulation of ER negative CSCs.

Author: Hannah HarrisonBruno M SimoesLynsey RogersonSacha J HowellGoran LandbergRobert B Clarke
Credits/Source: Breast Cancer Research 2013, 15:R21

Published on: 2013-03-08

News Provider: 7thSpace Interactive / EUPB Press Office

Copyright by the authors listed above - made available via BioMedCentral (Open Access). Please make sure to read our disclaimer prior to contacting 7thSpace Interactive. To contact our editors, visit our online helpdesk. If you wish submit your own press release, click here.

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