<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang J</submitter><funding>CAMS Innovation Fund for Medical Sciences</funding><pagination>225</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6136228</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>37(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Tumor recurrence, the chief reason for poor prognosis of glioma, is largely attributed to glioma stem cells (GSCs) and epithelial-mesenchymal transition (EMT). However, the mechanisms among them remain unknown. Here, we determined whether leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5), known as a stem cell marker for colon cancer and gastric cancer, can serve as a novel GSC marker involved in EMT and a therapeutic target in glioma.&lt;h4>Methods&lt;/h4>Stemness properties were examined in FACS-isolated LGR5&lt;sup>+&lt;/sup>/LGR5&lt;sup>-&lt;/sup> cells. Reported stem cell markers, EMT and the Wnt/β-catenin pathway were examined in stable LGR5 knockdown or overexpressed GSCs by Western Blot. The treatment experiment was performed in an intracranial orthotopic xenograft</pubmed_abstract><journal>Journal of experimental &amp; clinical cancer research : CR</journal><pubmed_title>LGR5, a novel functional glioma stem cell marker, promotes EMT by activating the Wnt/β-catenin pathway and predicts poor survival of glioma patients.</pubmed_title><pmcid>PMC6136228</pmcid><funding_grant_id>Nos. 2016-I2M-3-013, 2017-I2M-3-005</funding_grant_id><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Zhan P</pubmed_authors><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Ran Y</pubmed_authors><pubmed_authors>Wan J</pubmed_authors><pubmed_authors>Cai H</pubmed_authors></additional><is_claimable>false</is_claimable><name>LGR5, a novel functional glioma stem cell marker, promotes EMT by activating the Wnt/β-catenin pathway and predicts poor survival of glioma patients.</name><description>&lt;h4>Background&lt;/h4>Tumor recurrence, the chief reason for poor prognosis of glioma, is largely attributed to glioma stem cells (GSCs) and epithelial-mesenchymal transition (EMT). However, the mechanisms among them remain unknown. Here, we determined whether leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5), known as a stem cell marker for colon cancer and gastric cancer, can serve as a novel GSC marker involved in EMT and a therapeutic target in glioma.&lt;h4>Methods&lt;/h4>Stemness properties were examined in FACS-isolated LGR5&lt;sup>+&lt;/sup>/LGR5&lt;sup>-&lt;/sup> cells. Reported stem cell markers, EMT and the Wnt/β-catenin pathway were examined in stable LGR5 knockdown or overexpressed GSCs by Western Blot. The treatment experiment was performed in an intracranial orthotopic xenograft</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Sep</publication><modification>2026-06-13T04:01:09.653Z</modification><creation>2019-03-26T23:56:01Z</creation></dates><accession>S-EPMC6136228</accession><cross_references><pubmed>30208924</pubmed><doi>10.1186/s13046-018-0864-6</doi></cross_references></HashMap>