<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xin H</submitter><funding>National Natural Science Foundation of China</funding><pagination>30</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6325824</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>MicroRNA-196a-5p (miR-196a-5p) has been reported to be involved in the metastatic process of several cancers. In present work, we aimed to investigate the effects of miR-196a-5p and its potential target IκBα on migration, invasion and epithelial-mesenchymal transition (EMT) of colorectal cancer (CRC) cells.&lt;h4>Methods&lt;/h4>CCK-8 assay, wound healing assay and cell invasion assay were performed to evaluate the cell proliferation, migration and invasion. In vivo metastasis models were used to investigate the tumor metastasis ability. Real-time PCR, immunofluorescence staining or western blot were utilized to detect the expression of miR-196a-5p, IκBα, p-IκBα, nuclear p65 and EMT markers including E-cadherin, N-cadherin and fibronectin. Dual luciferase reporter assay was car</pubmed_abstract><journal>BMC cancer</journal><pubmed_title>miR-196a-5p promotes metastasis of colorectal cancer via targeting IκBα.</pubmed_title><pmcid>PMC6325824</pmcid><funding_grant_id>81470086</funding_grant_id><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Xin H</pubmed_authors></additional><is_claimable>false</is_claimable><name>miR-196a-5p promotes metastasis of colorectal cancer via targeting IκBα.</name><description>&lt;h4>Background&lt;/h4>MicroRNA-196a-5p (miR-196a-5p) has been reported to be involved in the metastatic process of several cancers. In present work, we aimed to investigate the effects of miR-196a-5p and its potential target IκBα on migration, invasion and epithelial-mesenchymal transition (EMT) of colorectal cancer (CRC) cells.&lt;h4>Methods&lt;/h4>CCK-8 assay, wound healing assay and cell invasion assay were performed to evaluate the cell proliferation, migration and invasion. In vivo metastasis models were used to investigate the tumor metastasis ability. Real-time PCR, immunofluorescence staining or western blot were utilized to detect the expression of miR-196a-5p, IκBα, p-IκBα, nuclear p65 and EMT markers including E-cadherin, N-cadherin and fibronectin. Dual luciferase reporter assay was car</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-04T18:56:15.927Z</modification><creation>2019-03-26T22:36:25Z</creation></dates><accession>S-EPMC6325824</accession><cross_references><pubmed>30621631</pubmed><doi>10.1186/s12885-018-5245-1</doi></cross_references></HashMap>