Daniel Martínez
@dmartimarti.bsky.social
120 followers 410 following 12 posts
Postdoctoral researcher at Cabreiro Lab. MRC/LMS. Imperial College London. I'm full of microbes, so I study them. Or they study themselves using me. Who knows. https://dmartimarti.github.io/
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dmartimarti.bsky.social
This work has been a wonderful conclusion of many years of hard work. I'm very happy to have worked with great scientists along the way, and I'm excited for the opportunities this research will open.
dmartimarti.bsky.social
Yes, it matters! In collab with chemists at Newcastle University, we synthesized the pure bacterial form, it was more potent. Then we engineered a trimethyl ester version that was even more effective at stopping cancer cell growth. ⚗️
dmartimarti.bsky.social
Finally, a super interesting thing we found. We'd been using a commercial racemic mixture of the two 2-MiCit enantiomers (2R,3S/2S,3R). But bacteria naturally produce only one of them: the (2R,3S) form. Does it matter?
dmartimarti.bsky.social
A 2-MiCit - drug screening revealed that 2-MiCit synergises with nucleotide antimetabolites such as 5-FU! Proteomics revealed their joint effect greatly affects p53 and pyrimidine metabolism, and make HCT116 spheroids really struggle to grow.
dmartimarti.bsky.social
How does 2-MiCit work? It hits the cell's mitochondria, impairing respiration. RNA-seq revealed this disrupts the cell cycle, DNA replication, and nucleotide metabolism. Crucially, it activates the p53 tumor suppressor pathway, which we confirmed with @alexisbarr.bsky.social
dmartimarti.bsky.social
We found 2-MiCit powerfully inhibits proliferation across 20 cancer cell lines and shrinks 3D tumor spheroids. In a fly model of colon cancer (thanks @cochemelab.bsky.social !), 2-MiCit treatment reduced tumor spread and extended the flies' lifespan!
dmartimarti.bsky.social
So, is this bacterial metabolite relevant in humans? With help from @kaletalab.bsky.social we predicted its production is significantly higher in the gut microbiomes of colorectal cancer patients. It is also present in cancer-associated microbiomes.

What does it actually do to cancer cells?
dmartimarti.bsky.social
A gene-nutrient screen pointed to a key mechanism: metabolic rewiring downstream of pyruvate, affecting the TCA. After many more experiments using C. elegans one culprit emerged: 2-MiCit, a metabolite from the bacterial methylcitrate cycle! 🎯
dmartimarti.bsky.social
Using a 4-way screening (bacteria + worm + drug + nutrient) we observed that sugars were able to impair 5-FU activity in C. elegans when fed with the the salvage pathway triple mutant, a super resistant strain for 5-FU effects.
dmartimarti.bsky.social
We started with a basic question: how does nutrition affect the drug 5-FU? Using C. elegans & E. coli we saw the drug's effect drastically changed depending on the bacterial strain and the nutrients in their environment! We tested >70 different E. coli strains that further confirmed this! 🧪
Reposted by Daniel Martínez