HSP40 interacts with pyruvate kinase M2 and regulates glycolysis and cell proliferation in tumor cells

Pyruvate kinase M2 (PKM2) is predominantly expressed in cancers, which is considered as a key regulator of the Warburg effect. In this study, HSP40 was identified as a novel binding partner of PKM2. HSP40-PKM2 association destabilized PKM2 protein through HSC70. In the presence of HSP40, PKM2 protei...

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Veröffentlicht in:PloS one 2014-03, Vol.9 (3), p.e92949-e92949
Hauptverfasser: Huang, Liangqian, Yu, Zhenhai, Zhang, Teng, Zhao, Xiaoping, Huang, Gang
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Sprache:eng
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Zusammenfassung:Pyruvate kinase M2 (PKM2) is predominantly expressed in cancers, which is considered as a key regulator of the Warburg effect. In this study, HSP40 was identified as a novel binding partner of PKM2. HSP40-PKM2 association destabilized PKM2 protein through HSC70. In the presence of HSP40, PKM2 protein level and PKM2-mediated PDK1 expression were down-regulated. Moreover, HSP40 was involved in regulating glucose metabolism on PKM2 dependent way and at the mean time had an effect on mitochondrial oxygen respiration. In line with inhibition effect of HSP40 on glycolysis, the growth of cancer cells was inhibited by HSP40.Our data provided a new regulation mechanism of PKM2, which suggested a new therapeutic target for cancer therapy.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0092949