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Upregulated KDM4B promotes prostate cancer cell proliferation by activating autophagy |
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| Authors: | Jianjun Sha Qing Han Chenfei Chi Yinjie Zhu Jiahua Pan Baijun Dong Yiran Huang Weiliang Xia Wei Xue |
| Affiliation: | 1. Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China Jianjun Sha and Qing Han contributed equally to the study.;2. School of Biomedical Engineering, Shanghai Jiaotong University, Shanghai, China Jianjun Sha and Qing Han contributed equally to the study.;3. Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China School of Biomedical Engineering, Shanghai Jiaotong University, Shanghai, China;4. Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China;5. School of Biomedical Engineering, Shanghai Jiaotong University, Shanghai, China |
| Abstract: | Castration-resistant prostate cancer (CRPC) causes most of the deaths in patients with prostate cancer (PCa). The androgen receptor (AR) axis plays an important role in castration resistance. Emerging studies showed that the lysine demethylase KDM4B is a key molecule in AR signaling and turnover, and autophagy plays an important role in CRPC. However, little is known about whether KDM4B promotes CRPC progression by regulating autophagy. Here we used an androgen-independent LNCaP (LNCaP-AI) cell line to assay aberrant KDM4B expression using qPCR and western blot analysis and investigated the function of KDM4B in regulating cell proliferation. We found that KDM4B was markedly increased in LNCaP-AI cells compared with LNCaP cells. KDM4B level was significantly correlated with the Gleason score in PCa tissues. In vitro, KDM4B overexpression in CRPC cells promoted cell proliferation, whereas knockdown of KDM4B significantly inhibited cell proliferation. Upregulated KDM4B contributed to activate Wnt/β-catenin signaling and autophagy. Moreover, KDM4B activated autophagy by regulating the Wnt/β-catenin signaling. Finally, we demonstrated that autophagy inhibition attenuated KDM4B-induced CRPC cell proliferation. Our results provided novel insights into the function of KDM4B-driven CRPC development and indicated that KDM4B may be served as a potential target for CRPC therapy. |
| Keywords: | autophagy cell proliferation CRPC KDM4B prostate cancer |