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The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration

The high-mobility group box 1 (HMGB1) protein has a central role in immunological antitumour defense. Here we show that natural killer cell-derived HMGB1 directly eliminates cancer cells by triggering metabolic cell death. HMGB1 allosterically inhibits the tetrameric pyruvate kinase isoform M2, thus...

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Autores principales: Gdynia, Georg, Sauer, Sven W., Kopitz, Jürgen, Fuchs, Dominik, Duglova, Katarina, Ruppert, Thorsten, Miller, Matthias, Pahl, Jens, Cerwenka, Adelheid, Enders, Markus, Mairbäurl, Heimo, Kamiński, Marcin M., Penzel, Roland, Zhang, Christine, Fuller, Jonathan C., Wade, Rebecca C., Benner, Axel, Chang-Claude, Jenny, Brenner, Hermann, Hoffmeister, Michael, Zentgraf, Hanswalter, Schirmacher, Peter, Roth, Wilfried
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786644/
https://www.ncbi.nlm.nih.gov/pubmed/26948869
http://dx.doi.org/10.1038/ncomms10764
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author Gdynia, Georg
Sauer, Sven W.
Kopitz, Jürgen
Fuchs, Dominik
Duglova, Katarina
Ruppert, Thorsten
Miller, Matthias
Pahl, Jens
Cerwenka, Adelheid
Enders, Markus
Mairbäurl, Heimo
Kamiński, Marcin M.
Penzel, Roland
Zhang, Christine
Fuller, Jonathan C.
Wade, Rebecca C.
Benner, Axel
Chang-Claude, Jenny
Brenner, Hermann
Hoffmeister, Michael
Zentgraf, Hanswalter
Schirmacher, Peter
Roth, Wilfried
author_facet Gdynia, Georg
Sauer, Sven W.
Kopitz, Jürgen
Fuchs, Dominik
Duglova, Katarina
Ruppert, Thorsten
Miller, Matthias
Pahl, Jens
Cerwenka, Adelheid
Enders, Markus
Mairbäurl, Heimo
Kamiński, Marcin M.
Penzel, Roland
Zhang, Christine
Fuller, Jonathan C.
Wade, Rebecca C.
Benner, Axel
Chang-Claude, Jenny
Brenner, Hermann
Hoffmeister, Michael
Zentgraf, Hanswalter
Schirmacher, Peter
Roth, Wilfried
author_sort Gdynia, Georg
collection PubMed
description The high-mobility group box 1 (HMGB1) protein has a central role in immunological antitumour defense. Here we show that natural killer cell-derived HMGB1 directly eliminates cancer cells by triggering metabolic cell death. HMGB1 allosterically inhibits the tetrameric pyruvate kinase isoform M2, thus blocking glucose-driven aerobic respiration. This results in a rapid metabolic shift forcing cells to rely solely on glycolysis for the maintenance of energy production. Cancer cells can acquire resistance to HMGB1 by increasing glycolysis using the dimeric form of PKM2, and employing glutaminolysis. Consistently, we observe an increase in the expression of a key enzyme of glutaminolysis, malic enzyme 1, in advanced colon cancer. Moreover, pharmaceutical inhibition of glutaminolysis sensitizes tumour cells to HMGB1 providing a basis for a therapeutic strategy for treating cancer.
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spelling pubmed-47866442016-03-16 The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration Gdynia, Georg Sauer, Sven W. Kopitz, Jürgen Fuchs, Dominik Duglova, Katarina Ruppert, Thorsten Miller, Matthias Pahl, Jens Cerwenka, Adelheid Enders, Markus Mairbäurl, Heimo Kamiński, Marcin M. Penzel, Roland Zhang, Christine Fuller, Jonathan C. Wade, Rebecca C. Benner, Axel Chang-Claude, Jenny Brenner, Hermann Hoffmeister, Michael Zentgraf, Hanswalter Schirmacher, Peter Roth, Wilfried Nat Commun Article The high-mobility group box 1 (HMGB1) protein has a central role in immunological antitumour defense. Here we show that natural killer cell-derived HMGB1 directly eliminates cancer cells by triggering metabolic cell death. HMGB1 allosterically inhibits the tetrameric pyruvate kinase isoform M2, thus blocking glucose-driven aerobic respiration. This results in a rapid metabolic shift forcing cells to rely solely on glycolysis for the maintenance of energy production. Cancer cells can acquire resistance to HMGB1 by increasing glycolysis using the dimeric form of PKM2, and employing glutaminolysis. Consistently, we observe an increase in the expression of a key enzyme of glutaminolysis, malic enzyme 1, in advanced colon cancer. Moreover, pharmaceutical inhibition of glutaminolysis sensitizes tumour cells to HMGB1 providing a basis for a therapeutic strategy for treating cancer. Nature Publishing Group 2016-03-07 /pmc/articles/PMC4786644/ /pubmed/26948869 http://dx.doi.org/10.1038/ncomms10764 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gdynia, Georg
Sauer, Sven W.
Kopitz, Jürgen
Fuchs, Dominik
Duglova, Katarina
Ruppert, Thorsten
Miller, Matthias
Pahl, Jens
Cerwenka, Adelheid
Enders, Markus
Mairbäurl, Heimo
Kamiński, Marcin M.
Penzel, Roland
Zhang, Christine
Fuller, Jonathan C.
Wade, Rebecca C.
Benner, Axel
Chang-Claude, Jenny
Brenner, Hermann
Hoffmeister, Michael
Zentgraf, Hanswalter
Schirmacher, Peter
Roth, Wilfried
The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title_full The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title_fullStr The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title_full_unstemmed The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title_short The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
title_sort hmgb1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786644/
https://www.ncbi.nlm.nih.gov/pubmed/26948869
http://dx.doi.org/10.1038/ncomms10764
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