<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(1)</volume><submitter>Hu P</submitter><pubmed_abstract>Acidosis is a significant feature of the tumor microenvironment in glioma, and it is closely related to multiple biological functions of cancer stem cells. Here, we found that the self-renewal ability, the mitochondrial activity and ATP production were elevated in stem cell-like glioma cells (SLCs) under acidic microenvironment, which promoted and maintained the stemness of SLCs. Under acidosis, 25-hydroxy vitamin D&lt;sub>3&lt;/sub>-24-hydroxylase (CYP24A1) was upregulated and catalyzed the fast degradation of 1α,25(OH)&lt;sub>2&lt;/sub>D&lt;sub>3&lt;/sub>. We further revealed that the active form of vitamin D (1α,25(OH)&lt;sub>2&lt;/sub>D&lt;sub>3&lt;/sub>) could inhibit the expression of stemness markers, attenuate acidosis-induced increase of self-renewal ability and mitochondrial respiration in stem cell-like glio</pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>25</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6328565</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Acidosis enhances the self-renewal and mitochondrial respiration of stem cell-like glioma cells through CYP24A1-mediated reduction of vitamin D.</pubmed_title><pmcid>PMC6328565</pmcid><pubmed_authors>Peng X</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Han W</pubmed_authors><pubmed_authors>Jiang T</pubmed_authors><pubmed_authors>Wei Z</pubmed_authors><pubmed_authors>Wu F</pubmed_authors><pubmed_authors>Yuan J</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Qiang B</pubmed_authors><pubmed_authors>Wei Q</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Yin B</pubmed_authors><pubmed_authors>Tian N</pubmed_authors><pubmed_authors>Hu P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Acidosis enhances the self-renewal and mitochondrial respiration of stem cell-like glioma cells through CYP24A1-mediated reduction of vitamin D.</name><description>Acidosis is a significant feature of the tumor microenvironment in glioma, and it is closely related to multiple biological functions of cancer stem cells. Here, we found that the self-renewal ability, the mitochondrial activity and ATP production were elevated in stem cell-like glioma cells (SLCs) under acidic microenvironment, which promoted and maintained the stemness of SLCs. Under acidosis, 25-hydroxy vitamin D&lt;sub>3&lt;/sub>-24-hydroxylase (CYP24A1) was upregulated and catalyzed the fast degradation of 1α,25(OH)&lt;sub>2&lt;/sub>D&lt;sub>3&lt;/sub>. We further revealed that the active form of vitamin D (1α,25(OH)&lt;sub>2&lt;/sub>D&lt;sub>3&lt;/sub>) could inhibit the expression of stemness markers, attenuate acidosis-induced increase of self-renewal ability and mitochondrial respiration in stem cell-like glio</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-04T10:13:28.19Z</modification><creation>2019-03-26T22:36:28Z</creation></dates><accession>S-EPMC6328565</accession><cross_references><pubmed>30631035</pubmed><doi>10.1038/s41419-018-1242-1</doi></cross_references></HashMap>