<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tang C</submitter><funding>Laboratory Animal Scientific Research Project of Zhejiang Province, China</funding><pagination>2119-2131</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8806792</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>The long non-coding RNAs (lncRNAs) participate in modulating numerous important cancer phenotypes via formation of RNA-protein complex. TINCR (terminal differentiation-induced lncRNA) modulates cancer cell behavior in many human malignancies, such as hepatocellular carcinoma (HCC). Herein, we proposed to investigate the underlying mechanism by which TINCR regulates HCC progression via formation of RNA-protein. RNA pulldown, LC-MS/MS, bioinformatics analysis, and RNA immunoprecipitation (RIP) assays were employed to identify TINCR-interacting protein TCPTP in HCC cells. The siRNAs for TINCR and TCPTP were transfected into HCC cells. The plasmids encoding full length or the 1-360 nt deletion of TINCR were generated and applied to cell transfection. The CCK-8, colony formation, EdU, wound hea</pubmed_abstract><journal>Bioengineered</journal><pubmed_title>Long non-coding RNA TINCR promotes hepatocellular carcinoma proliferation and invasion via STAT3 signaling by direct interacting with T-cell protein tyrosine phosphatase (TCPTP).</pubmed_title><pmcid>PMC8806792</pmcid><funding_grant_id>No. 2018C37088</funding_grant_id><pubmed_authors>Bao Y</pubmed_authors><pubmed_authors>Tang C</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Du H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long non-coding RNA TINCR promotes hepatocellular carcinoma proliferation and invasion via STAT3 signaling by direct interacting with T-cell protein tyrosine phosphatase (TCPTP).</name><description>The long non-coding RNAs (lncRNAs) participate in modulating numerous important cancer phenotypes via formation of RNA-protein complex. TINCR (terminal differentiation-induced lncRNA) modulates cancer cell behavior in many human malignancies, such as hepatocellular carcinoma (HCC). Herein, we proposed to investigate the underlying mechanism by which TINCR regulates HCC progression via formation of RNA-protein. RNA pulldown, LC-MS/MS, bioinformatics analysis, and RNA immunoprecipitation (RIP) assays were employed to identify TINCR-interacting protein TCPTP in HCC cells. The siRNAs for TINCR and TCPTP were transfected into HCC cells. The plasmids encoding full length or the 1-360 nt deletion of TINCR were generated and applied to cell transfection. The CCK-8, colony formation, EdU, wound hea</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2026-04-08T07:17:17.818Z</modification><creation>2024-10-18T03:06:28.589Z</creation></dates><accession>S-EPMC8806792</accession><cross_references><pubmed>34057016</pubmed><doi>10.1080/21655979.2021.1930336</doi></cross_references></HashMap>