Hormone Treatment Linked to Development of Aggressive Cancer

In a paper published in the November 26, 2018, online edition of the journal Nature Medicine, investigators at Cedars-Sinai Medical Center (Los Angeles, CA, USA) identified the transcription factor ONECUT2 (OC2) as a master regulator of AR networks in metastatic castration-resistant prostate cancer (mCRPC).

The ONECUT2 (one cut homeobox 2) gene encodes a member of the onecut family of transcription factors, which are characterized by a cut domain and an atypical homeodomain. The OC2 protein binds to specific DNA sequences and stimulates expression of target genes, including genes involved in melanocyte and hepatocyte differentiation.

In the current study, OC2 was found to act as a survival factor in mCRPC models, suppressing the AR transcriptional program by direct regulation of AR target genes. It also activated genes associated with neural differentiation and progression to lethal disease. Furthermore, OC2 was active in a substantial subset of human prostate adenocarcinoma and neuroendocrine tumors.

Following up, the investigators identified the compound CSRM617, which counteracted the action of onecut2. They showed that CSRM617 significantly reduced the size of prostate cancer metastases in mice.

"We need fresh strategies to prevent prostate cancer from turning deadly for the thousands of men whose disease metastasizes and withstands hormone therapy," said senior author Dr. Michael Freeman, professor of surgery and biomedical sciences at Cedars-Sinai Medical Center. "Our research suggested that onecut2 is a master regulator of lethal prostate cancer that may be a useful therapeutic target in up to a third of patients whose cancer spreads and evades hormone therapy."

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