The transcription factor EHF is highly expressed in the lactating mammary gland, but its role in mammary development and tumorigenesis is not fully understood. Utilizing a mouse model of Ehf deletion, herein, we demonstrate that loss of Ehf impairs mammary lobuloalveolar differentiation at late pregnancy, indicated by significantly reduced levels of milk genes and milk lipids, fewer differentiated alveolar cells, and an accumulation of alveolar progenitor cells. Further, deletion of Ehf increased proliferative capacity and attenuated prolactin-induced alveolar differentiation in mammary organoids. Ehf deletion also increased tumor incidence in the MMTV-PyMT mammary tumor model and increased the proliferative capacity of mammary tumor organoids, while low EHF expression was associated with higher tumor grade and poorer outcome in luminal A and basal human breast cancers. Collectively, these findings establish EHF as a non-redundant regulator of mammary alveolar differentiation and a putative suppressor of mammary tumorigenesis.
Funding
This project was supported in part by an Austin Health Medical Research Foundation (AMRF) grant (2–1293) and the Operational Infrastructure Support Program, Victorian Government, Australia. C.M.R., N.V., S.G., L.J.J. and R.J.M. were supported by La Trobe University Australian Postgraduate Scholarships. The ONJCRI microscopy platform is supported by an equipment grant from the Australian Cancer Research Foundation, 2016. Y.C. was supported by an MRFF Investigator grant (1176199). P.J.M. was supported by an NHMRC L3 Investigator grant (2009965). J.E.V. was supported by an NHMRC Fellowship (1102742). B.P. was supported by a Victorian Cancer Agency (VCA) mid-career fellowship (MCRF21002). J.M.M. was supported by an NHMRC Senior Research Fellowship (1046092).