<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nittayaboon K</submitter><funding>National Science, Research and Innovation Fund (NSRF) and Prince of Songkla University</funding><funding>Postdoctoral Fellowship program from Faculty of Medicine, Prince of Songkla University</funding><pagination>1050</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12299787</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(7)</volume><pubmed_abstract>&lt;b>Background:&lt;/b> Bone marrow mesenchymal stem cells (BM-MSCs) are significant in chemo- and radiotherapy resistance. Previous research has focused on BM-MSCs, demonstrating their functional involvement in cancer progression as mediators in the tumor microenvironment. They play multiple roles in tumorigenesis, angiogenesis, and metastasis. BM-MSC-derived exosomes (BM-MSCs-exo) are small vesicles, typically 50-300 nm in diameter, isolated from BM-MSCs. Some studies have demonstrated the tumor-suppressive effects of BM-MSCs-exo. &lt;b>Objective:&lt;/b> This study aimed to investigate their role in modulating the impact of chemoradiotherapy (CRT) in different types of cervical cancer spheroid cells. &lt;b>Methods:&lt;/b> The spheroids after treatment were subject to size measurement, cell viability, and</pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pubmed_title>Bone Marrow Mesenchymal Stem Cell-Derived Exosomes Modulate Chemoradiotherapy Response in Cervical Cancer Spheroids.</pubmed_title><pmcid>PMC12299787</pmcid><funding_grant_id>MED6701155S</funding_grant_id><pubmed_authors>Nittayaboon K</pubmed_authors><pubmed_authors>Bissanum R</pubmed_authors><pubmed_authors>Navakanitworakul R</pubmed_authors><pubmed_authors>Molika P</pubmed_authors><pubmed_authors>Chumsuwan N</pubmed_authors><pubmed_authors>Leetanaporn K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bone Marrow Mesenchymal Stem Cell-Derived Exosomes Modulate Chemoradiotherapy Response in Cervical Cancer Spheroids.</name><description>&lt;b>Background:&lt;/b> Bone marrow mesenchymal stem cells (BM-MSCs) are significant in chemo- and radiotherapy resistance. Previous research has focused on BM-MSCs, demonstrating their functional involvement in cancer progression as mediators in the tumor microenvironment. They play multiple roles in tumorigenesis, angiogenesis, and metastasis. BM-MSC-derived exosomes (BM-MSCs-exo) are small vesicles, typically 50-300 nm in diameter, isolated from BM-MSCs. Some studies have demonstrated the tumor-suppressive effects of BM-MSCs-exo. &lt;b>Objective:&lt;/b> This study aimed to investigate their role in modulating the impact of chemoradiotherapy (CRT) in different types of cervical cancer spheroid cells. &lt;b>Methods:&lt;/b> The spheroids after treatment were subject to size measurement, cell viability, and</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2025-08-16T03:07:00.037Z</modification><creation>2025-08-16T03:07:00.037Z</creation></dates><accession>S-EPMC12299787</accession><cross_references><pubmed>40732337</pubmed><doi>10.3390/ph18071050</doi></cross_references></HashMap>