<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou T</submitter><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><pagination>2594</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11274508</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(14)</volume><pubmed_abstract>Antiandrogen is part of the standard-of-care treatment option for metastatic prostate cancer. However, prostate cancers frequently relapse, and the underlying resistance mechanism remains incompletely understood. This study seeks to investigate whether long non-coding RNAs (lncRNAs) contribute to the resistance against the latest antiandrogen drug, darolutamide. Our RNA sequencing analysis revealed significant overexpression of LOC730101 in darolutamide-resistant cancer cells compared to the parental cells. Elevated LOC730101 levels were also observed in clinical samples of metastatic castration-resistant prostate cancer (CRPC) compared to primary prostate cancer samples. Silencing LOC730101 with siRNA significantly impaired the growth of darolutamide-resistant cells. Additional RNA sequen</pubmed_abstract><journal>Cancers</journal><pubmed_title>LncRNA LOC730101 Promotes Darolutamide Resistance in Prostate Cancer by Suppressing miR-1-3p.</pubmed_title><pmcid>PMC11274508</pmcid><funding_grant_id>P30 CA046934</funding_grant_id><funding_grant_id>1R33AI133697-03A1</funding_grant_id><funding_grant_id>R33 AI133697</funding_grant_id><funding_grant_id>R01 CA211861</funding_grant_id><funding_grant_id>1R01CA211861-05A1</funding_grant_id><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Nguyen S</pubmed_authors><pubmed_authors>Zhou T</pubmed_authors><pubmed_authors>He B</pubmed_authors><pubmed_authors>Feng Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>LncRNA LOC730101 Promotes Darolutamide Resistance in Prostate Cancer by Suppressing miR-1-3p.</name><description>Antiandrogen is part of the standard-of-care treatment option for metastatic prostate cancer. However, prostate cancers frequently relapse, and the underlying resistance mechanism remains incompletely understood. This study seeks to investigate whether long non-coding RNAs (lncRNAs) contribute to the resistance against the latest antiandrogen drug, darolutamide. Our RNA sequencing analysis revealed significant overexpression of LOC730101 in darolutamide-resistant cancer cells compared to the parental cells. Elevated LOC730101 levels were also observed in clinical samples of metastatic castration-resistant prostate cancer (CRPC) compared to primary prostate cancer samples. Silencing LOC730101 with siRNA significantly impaired the growth of darolutamide-resistant cells. Additional RNA sequen</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-04-08T19:20:36.954Z</modification><creation>2025-04-19T13:10:33.618Z</creation></dates><accession>S-EPMC11274508</accession><cross_references><pubmed>39061232</pubmed><doi>10.3390/cancers16142594</doi></cross_references></HashMap>