<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang X</submitter><funding>Shenzhen Medical Research Funds</funding><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Guangdong Province</funding><funding>China Postdoctoral Science Foundation</funding><funding>China Postdoctoral Innovation Talent Support Program</funding><funding>National Key Research and Development Program of China</funding><pagination>e2406688</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11653702</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(47)</volume><pubmed_abstract>In epithelial ovarian cancer (EOC), platinum resistance, potentially mediated by cancer stem cells (CSCs), often leads to relapse and treatment failure. Here, the role of spindle pole body component 25 (SPC25) as a key determinant promoting stemness and platinum resistance in EOC cells, with its expression being correlated with adverse clinical outcomes is delineated. Mechanistically, SPC25 acts as a scaffolding platform, orchestrating the assembly of an SPC25/RIOK1/MYH9 trimeric complex, triggering RIOK1-mediated phosphorylation of MYH9 at Ser1943. This prompts MYH9 to disengage from the cytoskeleton, augmenting its nuclear accumulation, thus potentiating CTNNB1 transcription and subsequent activation of Wnt/β-catenin signaling. CBP1, a competitive inhibitory peptide, can disrupt the form</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Targeting the SPC25/RIOK1/MYH9 Axis to Overcome Tumor Stemness and Platinum Resistance in Epithelial Ovarian Cancer.</pubmed_title><pmcid>PMC11653702</pmcid><funding_grant_id>81902675</funding_grant_id><funding_grant_id>A2303050</funding_grant_id><funding_grant_id>BX20230441</funding_grant_id><funding_grant_id>2021A1515012476</funding_grant_id><funding_grant_id>2023M734041</funding_grant_id><funding_grant_id>82303157</funding_grant_id><funding_grant_id>2023A1515110871</funding_grant_id><funding_grant_id>82203113</funding_grant_id><funding_grant_id>82330082</funding_grant_id><funding_grant_id>2020YFA0509400</funding_grant_id><funding_grant_id>82173302</funding_grant_id><funding_grant_id>81530082</funding_grant_id><funding_grant_id>2021A1515010333</funding_grant_id><funding_grant_id>82030078</funding_grant_id><funding_grant_id>82171955</funding_grant_id><funding_grant_id>82373369</funding_grant_id><funding_grant_id>2023A1515012746</funding_grant_id><pubmed_authors>Zou H</pubmed_authors><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Pan Y</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Deng P</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>He L</pubmed_authors><pubmed_authors>Chen B</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Song L</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Shi D</pubmed_authors><pubmed_authors>Ouyang Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting the SPC25/RIOK1/MYH9 Axis to Overcome Tumor Stemness and Platinum Resistance in Epithelial Ovarian Cancer.</name><description>In epithelial ovarian cancer (EOC), platinum resistance, potentially mediated by cancer stem cells (CSCs), often leads to relapse and treatment failure. Here, the role of spindle pole body component 25 (SPC25) as a key determinant promoting stemness and platinum resistance in EOC cells, with its expression being correlated with adverse clinical outcomes is delineated. Mechanistically, SPC25 acts as a scaffolding platform, orchestrating the assembly of an SPC25/RIOK1/MYH9 trimeric complex, triggering RIOK1-mediated phosphorylation of MYH9 at Ser1943. This prompts MYH9 to disengage from the cytoskeleton, augmenting its nuclear accumulation, thus potentiating CTNNB1 transcription and subsequent activation of Wnt/β-catenin signaling. CBP1, a competitive inhibitory peptide, can disrupt the form</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-26T17:04:03.817Z</modification><creation>2025-04-06T15:25:52.715Z</creation></dates><accession>S-EPMC11653702</accession><cross_references><pubmed>39488790</pubmed><doi>10.1002/advs.202406688</doi></cross_references></HashMap>