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Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth

Mitochondrial dysfunction and significant changes in metabolic pathways accompany cancer development and are responsible for maintaining the tumor microenvironment. Normal mitochondria can trigger intrinsic apoptosis by releasing cytochrome c into the cytosol. The survival of malignant cells highly...

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Autores principales: Bencze, Gyula, Bencze, Szilvia, Rivera, Keith D., Watson, James D., Hidvegi, Mate, Orfi, Laszlo, Tonks, Nicholas K., Pappin, Darryl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447799/
https://www.ncbi.nlm.nih.gov/pubmed/32843660
http://dx.doi.org/10.1038/s41598-020-71118-3
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author Bencze, Gyula
Bencze, Szilvia
Rivera, Keith D.
Watson, James D.
Hidvegi, Mate
Orfi, Laszlo
Tonks, Nicholas K.
Pappin, Darryl J.
author_facet Bencze, Gyula
Bencze, Szilvia
Rivera, Keith D.
Watson, James D.
Hidvegi, Mate
Orfi, Laszlo
Tonks, Nicholas K.
Pappin, Darryl J.
author_sort Bencze, Gyula
collection PubMed
description Mitochondrial dysfunction and significant changes in metabolic pathways accompany cancer development and are responsible for maintaining the tumor microenvironment. Normal mitochondria can trigger intrinsic apoptosis by releasing cytochrome c into the cytosol. The survival of malignant cells highly depends on the suppression of this function. We validated that A250, a highly purified fraction of fermented wheat germ extract (FWGE), increases the carbon flux into the mitochondria, the expression of key elements of the Krebs cycle and oxidative phosphorylation (OXPHOS). The increased respiratory chain activity is related to the mitochondria’s ability to release cytochrome c into the cytosol, which triggers the apoptotic cascade. The 68% tumor growth inhibitory effect observed in the murine melanoma study is related to this effect, as proteomic analysis validated similar changes in mitochondrial protein levels in the isolated tumor tissue samples. Blood count data indicated that this effect was not accompanied by general toxicity. This study is significant, as it shows that a highly concentrated form of FWGE is an effective agent that increases normal mitochondrial functionality. The lack of hepatotoxic and general toxic effects makes A250 an excellent candidate targeting mitochondria function in cancer therapy.
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spelling pubmed-74477992020-08-26 Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth Bencze, Gyula Bencze, Szilvia Rivera, Keith D. Watson, James D. Hidvegi, Mate Orfi, Laszlo Tonks, Nicholas K. Pappin, Darryl J. Sci Rep Article Mitochondrial dysfunction and significant changes in metabolic pathways accompany cancer development and are responsible for maintaining the tumor microenvironment. Normal mitochondria can trigger intrinsic apoptosis by releasing cytochrome c into the cytosol. The survival of malignant cells highly depends on the suppression of this function. We validated that A250, a highly purified fraction of fermented wheat germ extract (FWGE), increases the carbon flux into the mitochondria, the expression of key elements of the Krebs cycle and oxidative phosphorylation (OXPHOS). The increased respiratory chain activity is related to the mitochondria’s ability to release cytochrome c into the cytosol, which triggers the apoptotic cascade. The 68% tumor growth inhibitory effect observed in the murine melanoma study is related to this effect, as proteomic analysis validated similar changes in mitochondrial protein levels in the isolated tumor tissue samples. Blood count data indicated that this effect was not accompanied by general toxicity. This study is significant, as it shows that a highly concentrated form of FWGE is an effective agent that increases normal mitochondrial functionality. The lack of hepatotoxic and general toxic effects makes A250 an excellent candidate targeting mitochondria function in cancer therapy. Nature Publishing Group UK 2020-08-25 /pmc/articles/PMC7447799/ /pubmed/32843660 http://dx.doi.org/10.1038/s41598-020-71118-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bencze, Gyula
Bencze, Szilvia
Rivera, Keith D.
Watson, James D.
Hidvegi, Mate
Orfi, Laszlo
Tonks, Nicholas K.
Pappin, Darryl J.
Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title_full Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title_fullStr Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title_full_unstemmed Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title_short Mito-oncology agent: fermented extract suppresses the Warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
title_sort mito-oncology agent: fermented extract suppresses the warburg effect, restores oxidative mitochondrial activity, and inhibits in vivo tumor growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447799/
https://www.ncbi.nlm.nih.gov/pubmed/32843660
http://dx.doi.org/10.1038/s41598-020-71118-3
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