<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>102</volume><submitter>Li G</submitter><funding>Wuxi City Department of Science and Technology</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Chemoresistance is a critical factor contributing to poor prognosis in clinical patients with cancer undergoing postoperative adjuvant chemotherapy. The role of gut microbiota in mediating resistance to tumour chemotherapy remains to be investigated.&lt;h4>Methods&lt;/h4>Patients with CRC were categorised into clinical benefit responders (CBR) and no clinical benefit responders (NCB) based on chemotherapy efficacy. Differential bacterial analysis using 16S rRNA sequencing revealed Desulfovibrio as a distinct microbe between the two groups. Employing a syngeneic transplantation model, we assessed the effect of Desulfovibrio on chemotherapy by measuring tumour burden, weight, and Ki-67 expression. We further explored the mechanisms underlying the compromised chemotherapeutic eff</pubmed_abstract><journal>EBioMedicine</journal><pagination>105041</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10950750</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Desulfovibrio desulfuricans and its derived metabolites confer resistance to FOLFOX through METTL3.</pubmed_title><pmcid>PMC10950750</pmcid><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Yan Y</pubmed_authors><pubmed_authors>Yang C</pubmed_authors><pubmed_authors>Mao Y</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Desulfovibrio desulfuricans and its derived metabolites confer resistance to FOLFOX through METTL3.</name><description>&lt;h4>Background&lt;/h4>Chemoresistance is a critical factor contributing to poor prognosis in clinical patients with cancer undergoing postoperative adjuvant chemotherapy. The role of gut microbiota in mediating resistance to tumour chemotherapy remains to be investigated.&lt;h4>Methods&lt;/h4>Patients with CRC were categorised into clinical benefit responders (CBR) and no clinical benefit responders (NCB) based on chemotherapy efficacy. Differential bacterial analysis using 16S rRNA sequencing revealed Desulfovibrio as a distinct microbe between the two groups. Employing a syngeneic transplantation model, we assessed the effect of Desulfovibrio on chemotherapy by measuring tumour burden, weight, and Ki-67 expression. We further explored the mechanisms underlying the compromised chemotherapeutic eff</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-07-14T23:42:45.364Z</modification><creation>2025-04-05T22:29:49.74Z</creation></dates><accession>S-EPMC10950750</accession><cross_references><pubmed>38484555</pubmed><doi>10.1016/j.ebiom.2024.105041</doi></cross_references></HashMap>