<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bai S</submitter><funding>NCI NIH HHS</funding><pagination>249-252</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6498725</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(3)</volume><pubmed_abstract>The development and progression of metastatic castration-resistant prostate cancer is the major challenge in the treatment of advanced prostate cancer. The androgen receptor signaling pathway remains active in metastatic castration-resistant prostate cancer. Docetaxel and cabazitaxel are the first- and second-line chemotherapy, respectively, for patients with metastatic castration-resistant prostate cancer. These two taxanes, in general, function by (i) inhibiting mitosis and inducing apoptosis and (ii) preventing microtubule-dependent cargo trafficking. In prostate cancer, taxanes have been reported to inhibit the nuclear translocation and activity of the androgen receptor. However, whether this is attainable or not clinically remains controversial. In this review, we will provide a compr</pubmed_abstract><journal>Asian journal of andrology</journal><pubmed_title>Impact of taxanes on androgen receptor signaling.</pubmed_title><pmcid>PMC6498725</pmcid><funding_grant_id>R01 CA188609</funding_grant_id><pubmed_authors>Bai S</pubmed_authors><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Zhang BY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of taxanes on androgen receptor signaling.</name><description>The development and progression of metastatic castration-resistant prostate cancer is the major challenge in the treatment of advanced prostate cancer. The androgen receptor signaling pathway remains active in metastatic castration-resistant prostate cancer. Docetaxel and cabazitaxel are the first- and second-line chemotherapy, respectively, for patients with metastatic castration-resistant prostate cancer. These two taxanes, in general, function by (i) inhibiting mitosis and inducing apoptosis and (ii) preventing microtubule-dependent cargo trafficking. In prostate cancer, taxanes have been reported to inhibit the nuclear translocation and activity of the androgen receptor. However, whether this is attainable or not clinically remains controversial. In this review, we will provide a compr</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May-Jun</publication><modification>2025-05-29T22:12:37.251Z</modification><creation>2025-05-29T22:12:37.251Z</creation></dates><accession>S-EPMC6498725</accession><cross_references><pubmed>29900882</pubmed><doi>10.4103/aja.aja_37_18</doi></cross_references></HashMap>