期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 298, 期 11, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jbc.2022.102561
关键词
-
资金
- National Science Foundation of China [92057104, 31970670, 32170736, 32000528]
- Fundamental Research Funds for the Central Universities
- Open Project of the CAS Key Laboratory of Innate Immunity and Chronic Disease
- Laboratory for Synthetic Chemistry and Chemical Biology under the Health@InnoHK Program by the Innovation and Technology Commission of Hong Kong
This study reveals a new protumor function of Aurora A by phosphorylating PKM2 during the S phase of the cell cycle to promote glycolysis and tumor growth. The spatial and temporal regulation of the specific kinase and PKM2 interaction is context dependent, showing intricate interconnectivity between cell cycle and glycolytic regulators.
Cancer cells have distinctive demands for intermediates from glucose metabolism for biosynthesis and energy in different cell cycle phases. However, how cell cycle regulators and glycolytic enzymes coordinate to orchestrate the essential metabolic processes are still poorly characterized. Here, we report a novel interaction between the mitotic kinase, Aurora A, and the glycolytic enzyme, pyruvate kinase M2 (PKM2), in the interphase of the cell cycle. We found Aurora A-mediated phosphorylation of PKM2 at threonine 45. This phosphoryla-tion significantly attenuated PKM2 enzymatic activity by reducing its tetramerization and also promoted glycolytic flux and the branching anabolic pathways. Replacing the endoge-nous PKM2 with a nonphosphorylated PKM2 T45A mutant inhibited glycolysis, glycolytic branching pathways, and tumor growth in both in vitro and in vivo models. Together, our study revealed a new protumor function of Aurora A through modulating a rate-limiting glycolytic enzyme, PKM2, mainly during the S phase of the cell cycle. Our findings also showed that although both Aurora A and Aurora B kinase phosphor-ylate PKM2 at the same residue, the spatial and temporal regulations of the specific kinase and PKM2 interaction are context dependent, indicating intricate interconnectivity be-tween cell cycle and glycolytic regulators.
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