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Mechanistically, A42 disrupts LONP1 function through dual pathways: (1) by inhibiting METTL3-mediated LONP1 mRNA m 6 A to negatively regulate LONP1 expression, and (2) by directly binding to LONP1, inducing conformational changes in the protease complex, thereby markedly inhibiting its oligomerization process and substrate hydrolytic activity

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