Inhibition of the androgen receptor induces a novel tumor promoter, ZBTB46, for prostate cancer metastasis

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17 Citations (Scopus)

Abstract

Current therapeutic regimens for prostate cancer focus on targeting androgen receptor (AR) signaling. However, the AR is a key factor in luminal epithelium differentiation and was shown to have a role as a tumor suppressor. Thus, its inhibition may activate oncogenic pathways that contribute to metastatic castration-resistant prostate cancer (CRPC). Herein, we report a novel tumor promoter, ZBTB46, which is negatively regulated by AR signaling via microRNA (miR)-1-mediated downregulation. ZBTB46 is associated with malignant prostate cancer and is essential for metastasis. Its overexpression can overcome the antitumor effects of miR-1 and promote androgen-independent proliferation. We demonstrated that ZBTB46 can transcriptionally regulate SNAI1, a key epithelial-to-mesenchymal transition (EMT) driver, which could contribute to induction of the EMT after androgen-deprivation therapy and metastasis. Our findings are supportive of the model that disruption of AR's function may predispose prostate cancer to progress to metastatic CRPC.

Original languageEnglish
Pages (from-to)6213-6224
Number of pages12
JournalOncogene
Volume36
Issue number45
DOIs
Publication statusPublished - Nov 9 2017

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

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