<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(6)</volume><submitter>Guo F</submitter><pubmed_abstract>The treatment of castration-resistant prostate cancer (CRPC) still faces many challenges. Docetaxel is a chemotherapeutic drug commonly used in CRPC patients. However, docetaxel-based chemotherapy usually causes docetaxel resistance, partially due to the resistance of CRPC cells to docetaxel-induced apoptosis. Here, we report that the deubiquitinating enzyme ubiquitin-specific protease 33 (USP33) inhibits docetaxel-induced apoptosis of prostate cancer cells, including androgen-independent prostate cancer cells. USP33 is overexpressed in prostate cancer cells and tissues. We found that knockdown or knockout of USP33 enhanced docetaxel-induced apoptosis of prostate cancer cells, accompanied by increased phosphorylation of the cJUN NH2-terminal kinase (JNK). After blocking docetaxel-induced J</pubmed_abstract><journal>Cell death and differentiation</journal><pagination>1938-1951</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7244590</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Deubiquitinating enzyme USP33 restrains docetaxel-induced apoptosis via stabilising the phosphatase DUSP1 in prostate cancer.</pubmed_title><pmcid>PMC7244590</pmcid><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Fang Z</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Guo F</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Yang B</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Shi X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deubiquitinating enzyme USP33 restrains docetaxel-induced apoptosis via stabilising the phosphatase DUSP1 in prostate cancer.</name><description>The treatment of castration-resistant prostate cancer (CRPC) still faces many challenges. Docetaxel is a chemotherapeutic drug commonly used in CRPC patients. However, docetaxel-based chemotherapy usually causes docetaxel resistance, partially due to the resistance of CRPC cells to docetaxel-induced apoptosis. Here, we report that the deubiquitinating enzyme ubiquitin-specific protease 33 (USP33) inhibits docetaxel-induced apoptosis of prostate cancer cells, including androgen-independent prostate cancer cells. USP33 is overexpressed in prostate cancer cells and tissues. We found that knockdown or knockout of USP33 enhanced docetaxel-induced apoptosis of prostate cancer cells, accompanied by increased phosphorylation of the cJUN NH2-terminal kinase (JNK). After blocking docetaxel-induced J</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2026-04-29T05:26:04.759Z</modification><creation>2022-02-10T13:09:51.102Z</creation></dates><accession>S-EPMC7244590</accession><cross_references><pubmed>31857702</pubmed><doi>10.1038/s41418-019-0473-8</doi></cross_references></HashMap>