<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Lou J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Breast cancer (BC) is a serious health threat to the patients. The present work explored the mechanism of miR-301b-3p and transforming growth factor-beta receptor 2 (TGFBR2 ) in affecting BC progression.&lt;h4>Methods&lt;/h4>The miR-301b-3p-inhibitor and si-TGFBR2 solution were added to the DEME/F12 medium to culture the BC and normal breast epithelial cell lines to prepare negative control, miR-301b-3p-IN and miR-301b-3p-IN+si-TGFBR2 in the two types of cell lines. The relative expression of target genes and the interference effect were analyzed by quantitative real-time PCR (qRT- PCR). Cell viability was detected applying cell counting kit-8 (CCK-8) assay. Transwell and wound healing assay were conducted to evaluate the invasion and migration of BC cells after miR-301b-3p in</pubmed_abstract><journal>PeerJ</journal><pagination>e18324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11546148</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiR-301b-3p promotes breast cancer development through inhibiting the expression of transforming growth factor-beta receptor 2.</pubmed_title><pmcid>PMC11546148</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Wu M</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Mao W</pubmed_authors><pubmed_authors>Ying X</pubmed_authors><pubmed_authors>Lou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiR-301b-3p promotes breast cancer development through inhibiting the expression of transforming growth factor-beta receptor 2.</name><description>&lt;h4>Background&lt;/h4>Breast cancer (BC) is a serious health threat to the patients. The present work explored the mechanism of miR-301b-3p and transforming growth factor-beta receptor 2 (TGFBR2 ) in affecting BC progression.&lt;h4>Methods&lt;/h4>The miR-301b-3p-inhibitor and si-TGFBR2 solution were added to the DEME/F12 medium to culture the BC and normal breast epithelial cell lines to prepare negative control, miR-301b-3p-IN and miR-301b-3p-IN+si-TGFBR2 in the two types of cell lines. The relative expression of target genes and the interference effect were analyzed by quantitative real-time PCR (qRT- PCR). Cell viability was detected applying cell counting kit-8 (CCK-8) assay. Transwell and wound healing assay were conducted to evaluate the invasion and migration of BC cells after miR-301b-3p in</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-07-09T13:19:59.77Z</modification><creation>2025-04-06T11:47:39.968Z</creation></dates><accession>S-EPMC11546148</accession><cross_references><pubmed>39525474</pubmed><doi>10.7717/peerj.18324</doi></cross_references></HashMap>