<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(9)</volume><submitter>Zhang S</submitter><pubmed_abstract>This study investigates a novel approach to overcome Vemurafenib resistance in BRAF-mutant Anaplastic thyroid carcinoma (ATC) using CRISPR/Cas9 gene editing and TMTP1-modified extracellular vesicles (TMTP1-sgBRAF-EVs). By knocking out the BRAF gene, the study elucidates Vemurafenib-induced ferroptosis mechanisms involving lipid peroxidation and reactive oxygen species (ROS) generation in ATC cells. The developed TMTP1-sgBRAF-EVs system demonstrates superior tumour-targeting and drug delivery capabilities, significantly enhancing Vemurafenib efficacy in both in vitro and in vivo models. This innovative combination of gene editing technology with a nanoparticle delivery system shows promising potential as a therapeutic strategy for treating aggressive BRAF-mutant ATC.</pubmed_abstract><journal>Journal of extracellular vesicles</journal><pagination>e70170</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12465009</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TMTP1-Modified Small Extracellular Vesicles Target BRAF Mutation in Anaplastic Thyroid Cancer Reversing Vemurafenib Resistance With CRISPR/Cas9 Delivery.</pubmed_title><pmcid>PMC12465009</pmcid><pubmed_authors>Bai T</pubmed_authors><pubmed_authors>Cai D</pubmed_authors><pubmed_authors>Feng M</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Ji Z</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Cheng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>TMTP1-Modified Small Extracellular Vesicles Target BRAF Mutation in Anaplastic Thyroid Cancer Reversing Vemurafenib Resistance With CRISPR/Cas9 Delivery.</name><description>This study investigates a novel approach to overcome Vemurafenib resistance in BRAF-mutant Anaplastic thyroid carcinoma (ATC) using CRISPR/Cas9 gene editing and TMTP1-modified extracellular vesicles (TMTP1-sgBRAF-EVs). By knocking out the BRAF gene, the study elucidates Vemurafenib-induced ferroptosis mechanisms involving lipid peroxidation and reactive oxygen species (ROS) generation in ATC cells. The developed TMTP1-sgBRAF-EVs system demonstrates superior tumour-targeting and drug delivery capabilities, significantly enhancing Vemurafenib efficacy in both in vitro and in vivo models. This innovative combination of gene editing technology with a nanoparticle delivery system shows promising potential as a therapeutic strategy for treating aggressive BRAF-mutant ATC.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T21:23:09.466Z</modification><creation>2026-05-01T03:11:02.714Z</creation></dates><accession>S-EPMC12465009</accession><cross_references><pubmed>41002137</pubmed><doi>10.1002/jev2.70170</doi></cross_references></HashMap>