Transcriptional Repression and Protein Degradation of the Ca2+-Activated K+ Channel KCa1.1 by Androgen Receptor Inhibition in Human Breast Cancer Cells

  • Front Physiol. 2018 Apr 16;9:312. doi: 10.3389/fphys.2018.00312.
Anowara Khatun  1 ,  Motoki Shimozawa  1 ,  Hiroaki Kito  1 ,  Mayu Kawaguchi  1 ,  Mayu Fujimoto  1 ,  Moe Ri  2 ,  Junko Kajikuri  2 ,  Satomi Niwa  1 ,  Masanori Fujii  1 ,  Susumu Ohya  1  2
Affiliations
  • 1. Division of Pathological Sciences, Department of Pharmacology, Kyoto Pharmaceutical University, Kyoto, Japan.
  • 2. Department of Pharmacology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
PMID: 29713287 DOI: 10.3389/fphys.2018.00312
Abstract

The large-conductance CA2+-activated K+ channel KCA1.1 plays an important role in the promotion of breast Cancer cell proliferation and metastasis. The Androgen Receptor (AR) is proposed as a therapeutic target for AR-positive advanced triple-negative breast Cancer. We herein investigated the effects of a treatment with antiandrogens on the functional activity, activation kinetics, transcriptional expression, and protein degradation of KCA1.1 in human breast Cancer MDA-MB-453 cells using Real-Time PCR, Western blotting, voltage-sensitive dye imaging, and whole-cell patch clamp recording. A treatment with the antiandrogen bicalutamide or enzalutamide for 48 h significantly suppressed (1) depolarization responses induced by paxilline (PAX), a specific KCA1.1 blocker and (2) PAX-sensitive outward currents induced by the depolarizing voltage step. The expression levels of KCA1.1 transcripts and proteins were significantly decreased in MDA-MB-453 cells, and the protein degradation of KCA1.1 mainly contributed to reductions in KCA1.1 activity. Among the eight regulatory β and γ subunits, LRRC26 alone was expressed at high levels in MDA-MB-453 cells and primary and metastatic breast Cancer tissues, whereas no significant changes were observed in the expression levels of LRRC26 and activation kinetics of PAX-sensitive outward currents in MDA-MB-453 cells by the treatment with antiandrogens. The treatment with antiandrogens up-regulated the expression of the ubiquitin E3 Ligases, FBW7, MDM2, and MDM4 in MDA-MB-453 cells, and the protein degradation of KCA1.1 was significantly inhibited by the respective siRNA-mediated blockade of FBW7 and MDM2. Based on these results, we concluded that KCA1.1 is an androgen-responsive gene in AR-positive breast Cancer cells, and its down-regulation through enhancements in its protein degradation by FBW7 and/or MDM2 may contribute, at least in part, to the antiproliferative and antimetastatic effects of antiandrogens in breast Cancer cells.

Keywords
Ca2+-activated K+ channel; KCa1.1; androgen receptor; antiandrogen; breast cancer; ubiquitin E3 ligase.
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