Cell Reports, Год журнала: 2025, Номер 44(4), С. 115441 - 115441
Опубликована: Март 18, 2025
Язык: Английский
Cell Reports, Год журнала: 2025, Номер 44(4), С. 115441 - 115441
Опубликована: Март 18, 2025
Язык: Английский
Developmental Cell, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
1Cancer Cell International, Год журнала: 2025, Номер 25(1)
Опубликована: Фев. 12, 2025
Язык: Английский
Процитировано
1Advanced Science, Год журнала: 2025, Номер unknown
Опубликована: Фев. 14, 2025
Lactate derived from aerobic glycolysis is crucial for DNA damage repair and chemoresistance. Nevertheless, it frequently noted that cancer cells depend on glutaminolysis to replenish essential metabolites. Whether how might enhance lactate production facilitate in remains unknown. Here, shown malate enzyme 2 (ME2), which metabolizes glutamine-derived pyruvate, contributes chemotherapy resistance ovarian cancer. Mechanistically, reduces the expression of glucose transporters impairs uptake cells. The resultant decrease intracellular levels triggers acetylation ME2 at lysine 156 by ACAT1, turn potentiates activity facilitates glutamine. ME2-derived development acquired chemoresistance subjected prolonged chemotherapy, primarily facilitating lactylation proteins involved homologous recombination repair. Targeting ACAT1 inhibit effectively reduced both vitro vivo models. These findings underscore significance acetylated ME2-mediated glutamine chemoresistance, particularly under conditions within cell, thereby complementing Warburg effect offering new perspectives metabolic links resistance.
Язык: Английский
Процитировано
1Food Bioscience, Год журнала: 2025, Номер unknown, С. 106185 - 106185
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
1Cell Reports, Год журнала: 2025, Номер 44(4), С. 115441 - 115441
Опубликована: Март 18, 2025
Язык: Английский
Процитировано
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