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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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Detalles Bibliográficos
Autores principales: Huang, Liangqian, Yu, Zhenhai, Zhang, Teng, Zhao, Xiaoping, Huang, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962495/
https://www.ncbi.nlm.nih.gov/pubmed/24658033
http://dx.doi.org/10.1371/journal.pone.0092949
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author Huang, Liangqian
Yu, Zhenhai
Zhang, Teng
Zhao, Xiaoping
Huang, Gang
author_facet Huang, Liangqian
Yu, Zhenhai
Zhang, Teng
Zhao, Xiaoping
Huang, Gang
author_sort Huang, Liangqian
collection PubMed
description 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.
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spelling pubmed-39624952014-03-24 HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells Huang, Liangqian Yu, Zhenhai Zhang, Teng Zhao, Xiaoping Huang, Gang PLoS One Research Article 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. Public Library of Science 2014-03-21 /pmc/articles/PMC3962495/ /pubmed/24658033 http://dx.doi.org/10.1371/journal.pone.0092949 Text en © 2014 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Huang, Liangqian
Yu, Zhenhai
Zhang, Teng
Zhao, Xiaoping
Huang, Gang
HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title_full HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title_fullStr HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title_full_unstemmed HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title_short HSP40 Interacts with Pyruvate Kinase M2 and Regulates Glycolysis and Cell Proliferation in Tumor Cells
title_sort hsp40 interacts with pyruvate kinase m2 and regulates glycolysis and cell proliferation in tumor cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962495/
https://www.ncbi.nlm.nih.gov/pubmed/24658033
http://dx.doi.org/10.1371/journal.pone.0092949
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