EZH2 Oncogenic Activity in Castration-Resistant Prostate Cancer Cells Is Polycomb-Independent
Harvard University · Dana-Farber Cancer Institute · +10 more institutions
Abstract
Epigenetic regulators represent a promising new class of therapeutic targets for cancer. Enhancer of zeste homolog 2 (EZH2), a subunit of Polycomb repressive complex 2 (PRC2), silences gene expression via its histone methyltransferase activity. We found that the oncogenic function of EZH2 in cells of castration-resistant prostate cancer is independent of its role as a transcriptional repressor. Instead, it involves the ability of EZH2 to act as a coactivator for critical transcription factors including the androgen receptor. This functional switch is dependent on phosphorylation of EZH2 and requires an intact methyltransferase domain. Hence, targeting the non-PRC2 function of EZH2 may have therapeutic efficacy…
Citation impact
- FWCI
- 22.84
- Percentile
- 100%
- References
- 46
Authors
22- KXKexin XuCorresponding
Harvard University, Dana-Farber Cancer Institute
- ZJZhenhua J. WuCorresponding
Dana-Farber Cancer Institute
- ACAnna C. Groner
Harvard University, Dana-Farber Cancer Institute
- HHHousheng Hansen He
Harvard University, Dana-Farber Cancer Institute
- CCChangmeng Cai
Beth Israel Deaconess Medical Center, Harvard University
Topics & keywords
- EZH2
- PRC2
- Prostate cancer
- Cancer research
- Histone methyltransferase
- Biology
- Epigenetics
- Repressor
- Good health and well-being