Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1053302 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR27220707_1.fastq.gz | Fastqsanger.gz | |||
| SRR27220707_2.fastq.gz | Fastqsanger.gz | |||
| SRR27220708_1.fastq.gz | Fastqsanger.gz | |||
| SRR27220708_2.fastq.gz | Fastqsanger.gz | |||
| SRR27220709_1.fastq.gz | Fastqsanger.gz |
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Project description:<p>Understanding how the microbiota produces regulatory metabolites is of significance for cancer and cancer therapy. Using a host-microbe-drug-nutrient 4-way screening approach, we evaluated the role of nutrition at the molecular level in the context of 5-fluorouracil toxicity. Notably, our screens identified the metabolite 2-methylisocitrate which was found to be produced and enriched in human tumor-associated microbiota. 2-methylisocitrate exhibits anti-proliferative properties across genetically- and tissue-diverse cancer cell lines, 3D spheroids and an in vivo Drosophila gut tumor model, where it reduced tumor dissemination and increased survival. Chemical landscape interaction screens identified drug-metabolite signatures and highlighted the synergy between 5-fluorouracil and 2-methylisocitrate. Multi-omic analyses revealed that 2-methylisocitrate acts via multiple cellular pathways linking metabolism and DNA damage to regulate chemotherapy. Finally, we converted 2-methylisocitrate into its trimethyl ester, thereby enhancing its potency. This work highlights the great impact of microbiome-derived metabolites on tumor proliferation, and their potential as promising co-adjuvants for cancer treatment.</p><p><br></p><p><strong>Targeted metabolomics - 2methylisocitrate</strong> is reported in the current study <strong>MTBLS9994</strong>.</p><p><strong>Targeted metabolomics - fluoronucleotides</strong> is reported in <strong>MTBLS9991</strong>.</p>
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Project description:<p>Understanding how the microbiota produces regulatory metabolites is of significance for cancer and cancer therapy. Using a host-microbe-drug-nutrient 4-way screening approach, we evaluated the role of nutrition at the molecular level in the context of 5-fluorouracil toxicity. Notably, our screens identified the metabolite 2-methylisocitrate which was found to be produced and enriched in human tumor-associated microbiota. 2-methylisocitrate exhibits anti-proliferative properties across genetically- and tissue-diverse cancer cell lines, 3D spheroids and an in vivo Drosophila gut tumor model, where it reduced tumor dissemination and increased survival. Chemical landscape interaction screens identified drug-metabolite signatures and highlighted the synergy between 5-fluorouracil and 2-methylisocitrate. Multi-omic analyses revealed that 2-methylisocitrate acts via multiple cellular pathways linking metabolism and DNA damage to regulate chemotherapy. Finally, we converted 2-methylisocitrate into its trimethyl ester, thereby enhancing its potency. This work highlights the great impact of microbiome-derived metabolites on tumor proliferation, and their potential as promising co-adjuvants for cancer treatment.</p><p><br></p><p><strong>Targeted metabolomics - fluoronucleotides</strong> is reported in the current study <strong>MTBLS9991</strong>.</p><p><strong>Targeted metabolomics - 2methylisocitrate</strong> is reported in <strong>MTBLS9994</strong>.</p>
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