<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>123(4)</volume><submitter>Wan G</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Human Schlafen 5 (SLFN5) has been reported to inhibit or promote cell invasion in tumours depending on their origin. However, its role in breast cancer (BRCA) is undetermined.&lt;h4>Methods&lt;/h4>Differential expression analyses using The Cancer Genome Atlas (TCGA) data, clinical samples and cell lines were performed. Lentiviral knockdown and overexpression experiments were performed to detect changes in cell morphology, molecular markers and invasion. Chromatin immunoprecipitation-sequencing (ChIP-Seq) and luciferase reporter assays were performed to detect the SLFN5-binding motif.&lt;h4>Results&lt;/h4>TCGA, clinical samples and cell lines showed that SLFN5 expression was negatively correlated with BRCA metastasis. SLFN5 knockdown induced epithelial-mesenchymal transition (EMT) an</pubmed_abstract><journal>British journal of cancer</journal><pagination>633-643</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7435190</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Human Schlafen 5 regulates reversible epithelial and mesenchymal transitions in breast cancer by suppression of ZEB1 transcription.</pubmed_title><pmcid>PMC7435190</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Gu X</pubmed_authors><pubmed_authors>Huang G</pubmed_authors><pubmed_authors>Lu C</pubmed_authors><pubmed_authors>Wan G</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Wu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human Schlafen 5 regulates reversible epithelial and mesenchymal transitions in breast cancer by suppression of ZEB1 transcription.</name><description>&lt;h4>Background&lt;/h4>Human Schlafen 5 (SLFN5) has been reported to inhibit or promote cell invasion in tumours depending on their origin. However, its role in breast cancer (BRCA) is undetermined.&lt;h4>Methods&lt;/h4>Differential expression analyses using The Cancer Genome Atlas (TCGA) data, clinical samples and cell lines were performed. Lentiviral knockdown and overexpression experiments were performed to detect changes in cell morphology, molecular markers and invasion. Chromatin immunoprecipitation-sequencing (ChIP-Seq) and luciferase reporter assays were performed to detect the SLFN5-binding motif.&lt;h4>Results&lt;/h4>TCGA, clinical samples and cell lines showed that SLFN5 expression was negatively correlated with BRCA metastasis. SLFN5 knockdown induced epithelial-mesenchymal transition (EMT) an</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2025-04-22T02:44:00.605Z</modification><creation>2022-02-11T15:49:11.662Z</creation></dates><accession>S-EPMC7435190</accession><cross_references><pubmed>32488136</pubmed><doi>10.1038/s41416-020-0873-z</doi></cross_references></HashMap>