PAK5-mediated PKM2 phosphorylation is critical for anaerobic glycolysis in endometriosis

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PAK5 is upregulated in endometriosis and promotes glycolysis by enhancing PKM2 stability, with PAK5-mediated PKM2 phosphorylation at Ser519 driving cell proliferation and metastasis.

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This paper investigated the role of p21-activated kinase 5 (PAK5) in endometriosis, examining PAK5 expression and functional effects in endometriosis models using PAK5 knockdown, the PAK5 inhibitor GNE 2861, and PAK5-knockout mice. The study found PAK5 was strikingly upregulated in endometriosis, and that reducing PAK5 activity blocked endometriosis development; it also reported that PAK5 promotes glycolysis by stabilizing PKM2 and that phosphorylation of PKM2 at Ser519 by PAK5 mediates endometriotic cell proliferation and metastasis. A key caveat explicitly stated in the provided text is limited to the overall study framing: detailed methodological or experimental limitations beyond these statements are not described in the excerpt. This paper is centrally about endometriosis — it identifies PAK5-mediated PKM2 phosphorylation (Ser519) as a driver of endometriosis glycolysis, proliferation, and metastasis.

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Abstract

P21-activated kinase 5 (PAK5) belongs to the PAK-II subfamily, which is an important regulator of cell survival, adhesion, and motility. However, the functions of PAK5 in endometriosis remain unclear. Here, PAK5 is strikingly upregulated in endometriosis. Furthermore, the knockdown of PAK5 or its inhibitor GNE 2861 blocks the development of endometriosis, which is equally demonstrated in PAK5-knockout mice. In addition, PAK5 promotes glycolysis by enhancing the protein stability of pyruvate kinase 2 (PKM2) in endometriotic cells, which is a key enzyme for glucose metabolism. Moreover, the phosphorylation of PKM2 at Ser519 by PAK5 mediates endometriosis cell proliferation and metastasis. Collectively, PAK5 plays an indispensable role in endometriosis. Our findings demonstrate that PAK5 is an important target for the treatment of endometriosis. Similar content being viewed by others

References

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Acknowledgements

The study was supported by research grants from the National Natural Science Foundation of China (Nos. 81972489 and 82003201), the National Natural Science Foundation of Shandong Province (No. ZR2020YQ58), Shandong Province College Science and Technology Plan Project (No. J17KA254), Projects of medical and health technology development program in Shandong province (No. 2018WS057). Author information Authors and Affiliations Corresponding authors Ethics declarations Conflict of interest Jiayi Lu, Xiaoyun Wang, Xiaodan Shi, Junyi Jiang, Lan Liu, Lu Liu, Chune Ren, Chao Lu, and Zhenhai Yu declare that they have no conflict of interest. This study was approved by the Ethics Committee of the Affiliated Hospital of Shandong Second Medical University and the study was performed in accordance with the ethical standards as laid down in the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards. Informed consent was obtained from all patients for being included in the study. All institutional and national guidelines for the care and use of laboratory animals were followed. Rights and permissions About this article Cite this article Lu, J., Wang, X., Shi, X. et al. PAK5-mediated PKM2 phosphorylation is critical for anaerobic glycolysis in endometriosis. Front. Med. 18, 1054–1067 (2024). https://doi.org/10.1007/s11684-024-1069-3 Received: Accepted: Published: Version of record: Issue date: DOI: https://doi.org/10.1007/s11684-024-1069-3

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mesh:D004715endometriosis

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Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Carrier Proteins Cell Proliferation Cell Proliferation Cell Proliferation

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