<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(10)</volume><submitter>Chen PC</submitter><pubmed_abstract>MicroRNAs (miRNAs) have been shown to play a crucial role in the progression of human cancers, including urothelial carcinoma (UC), the sixth-most common cancer in the world. Among them, miR-34a has been implicated in the regulation of cancer stem cells (CSCs); however, its role in UC has yet to be fully elucidated. In this study, bioinformatics and experimental analysis confirmed that miR-34a targets CD44 (a CSC surface marker) and c-Myc (a well-known cell cycle regulator) in UC. We found that, surprisingly, most UC cell lines and patient samples did express miR-34a, although epigenetic silencing by promoter hypermethylation of miR-34a expression was observed only in UMUC3 cells, and a subset of patient samples. Importantly, overexpression of c-Myc, a frequently amplified oncogene in UC, </pubmed_abstract><journal>Cancers</journal><pagination>E1457</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6826510</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>c-Myc Acts as a Competing Endogenous RNA to Sponge miR-34a, in the Upregulation of CD44, in Urothelial Carcinoma.</pubmed_title><pmcid>PMC6826510</pmcid><pubmed_authors>Jou YC</pubmed_authors><pubmed_authors>Huang WY</pubmed_authors><pubmed_authors>Huang WH</pubmed_authors><pubmed_authors>Chuang YM</pubmed_authors><pubmed_authors>Shen CH</pubmed_authors><pubmed_authors>Lin HY</pubmed_authors><pubmed_authors>Chan MWY</pubmed_authors><pubmed_authors>Lin RI</pubmed_authors><pubmed_authors>Lin JMJ</pubmed_authors><pubmed_authors>Chen PC</pubmed_authors><pubmed_authors>Yu CC</pubmed_authors></additional><is_claimable>false</is_claimable><name>c-Myc Acts as a Competing Endogenous RNA to Sponge miR-34a, in the Upregulation of CD44, in Urothelial Carcinoma.</name><description>MicroRNAs (miRNAs) have been shown to play a crucial role in the progression of human cancers, including urothelial carcinoma (UC), the sixth-most common cancer in the world. Among them, miR-34a has been implicated in the regulation of cancer stem cells (CSCs); however, its role in UC has yet to be fully elucidated. In this study, bioinformatics and experimental analysis confirmed that miR-34a targets CD44 (a CSC surface marker) and c-Myc (a well-known cell cycle regulator) in UC. We found that, surprisingly, most UC cell lines and patient samples did express miR-34a, although epigenetic silencing by promoter hypermethylation of miR-34a expression was observed only in UMUC3 cells, and a subset of patient samples. Importantly, overexpression of c-Myc, a frequently amplified oncogene in UC, </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Sep</publication><modification>2025-04-05T00:43:51.951Z</modification><creation>2020-05-21T19:57:29Z</creation></dates><accession>S-EPMC6826510</accession><cross_references><pubmed>31569404</pubmed><doi>10.3390/cancers11101457</doi></cross_references></HashMap>