
A breakthrough study uncovered the critical role of N7-guanosine methylation (m7G) of tRNAs, mediated by METTL1, in regulating cancer cell survival under stress conditions. The study demonstrates that m7G modification of tRNAs shields them from stress-induced cleavage, preventing the formation of 5' tRNA fragments. Loss of this modification activates stress response pathways, making cancer cells more vulnerable to stress. Additionally, the loss of METTL1 was found to inhibit tumor growth and increase cytotoxic stress in vivo. This discovery holds promise for enhancing the effectiveness of chemotherapy by targeting METTL1.
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