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10.1007/s12079-017-0378-6 http://scihub22266oqcxt.onion/10.1007/s12079-017-0378-6 C5362580!5362580!28255661     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Cell+Commun+Signal 2017 ; 11 (1): 89-91 Nephropedia Template TP {{tp|p=28255661|t=2017. CCN3-EZH2-AR feedback loop: new targets for enzalutamide and castration resistant prostate cancer |pdf=|usr=}}{{28255661}} gab.com Text CCN3-EZH2-AR feedback loop: new targets for enzalutamide and castration resistant prostate cancer JO: J Cell Commun Signal http://www.kidney.de/pget.php?&tw=1&pmid=28255661 #FOAvip The development of castration resistant prostate cancer and anti-androgen resistance remains one of the largest hurdles in the successful treatment of prostate cancer. Therefore, the identification of dysregulated pathways contributing to this resistance and determining ways to target these mechanisms is of utmost importance. In the recent publication in Cancer Research, Fong et al. identify a novel role for cytoplasmic CCN3 in prostate cancer progression and enzalutamide resistance. The authors demonstrate that CCN3 expression inhibits androgen receptor signaling and thereby suppresses enzalutamide-resistant prostate cancer cell proliferation, colony formation, and xenograft tumor growth. The data from this manuscript highlight an intriguing potential therapeutic target for the treatment of CRPC and are a critical step forwards towards treating enzalutamide resistant prostate cancer. Twit Text FOAVip CCN3-EZH2-AR feedback loop: new targets for enzalutamide and castration resistant prostate cancer ????J Cell Commun Signal http://www.kidney.de/pget.php?&tw=1&pmid=28255661 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28255661 #FOAvip English Wikipedia <ref>{{Cite pmid|28255661}}</ref> CCN3-EZH2-AR feedback loop: new targets for enzalutamide and castration resistant prostate cancer #MMPMID28255661 Armstrong CM; Gao AC J Cell Commun Signal 2017[Mar]; 11 (1): 89-91 PMID28255661show ga The development of castration resistant prostate cancer and anti-androgen resistance remains one of the largest hurdles in the successful treatment of prostate cancer. Therefore, the identification of dysregulated pathways contributing to this resistance and determining ways to target these mechanisms is of utmost importance. In the recent publication in Cancer Research, Fong et al. identify a novel role for cytoplasmic CCN3 in prostate cancer progression and enzalutamide resistance. The authors demonstrate that CCN3 expression inhibits androgen receptor signaling and thereby suppresses enzalutamide-resistant prostate cancer cell proliferation, colony formation, and xenograft tumor growth. The data from this manuscript highlight an intriguing potential therapeutic target for the treatment of CRPC and are a critical step forwards towards treating enzalutamide resistant prostate cancer. äCCN3-EZH2-AR feedback loop: new targets for enzalutamide and castratio(epmc).pdf DeepDyve Pubget Overpricing