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Chemoresistance in triple-negative breast cancer complicates patient management. In this study, researchers investigated the mechanisms behind this chemoresistance. They discovered that the protein arginine methyltransferase-1 (PRMT1) simultaneously methylates D-3-phosphoglycerate dehydrogenase (PHGDH) and the glycolytic enzymes PFKFB3 and PKM2 in tumour cells. This methylation would accelerate the production of methyl donors in tumour cells. On the other hand, the researchers showed links between these methylation pathways and fatty acid synthesis. The metabolites required for methylation and fatty acid synthesis would be enriched in triple-negative breast cancer cells, which could explain chemoresistance.

Source(s) :
Takehiro Yamamoto et al. PRMT1 sustains de novo fatty acid synthesis by methylating PHGDH to drive chemoresistance in triple-negative breast cancer. Cancer Res. 2024 Feb 22. ;

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