PAK5-mediated PKM2 phosphorylation is critical for anaerobic glycolysis in endometriosis
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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References (50)
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Cited by (4)
- Ubiquitination of PFKFB4 by CHIP regulates glycolysis and progression in endometriosis 2025
- Ubiquitination of PFKFB4 by CHIP regulates glycolysis and progression in endometriosis 2025
- Lactate-mediated immune suppression and MDSC expansion in endometriosis: Mechanisms and nanoparticle-targeted therapies 2025
- Warburg-like Metabolic Reprogramming in Endometriosis: From Molecular Mechanisms to Therapeutic Approaches 2025
Source provenance
- europepmc
- last seen: 2026-06-04T01:30:01.192114+00:00
- openalex
- last seen: 2026-06-04T00:00:01.174412+00:00
- pubmed
- last seen: 2026-06-04T00:32:22.903660+00:00