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The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela
Cancer cells have an unusual regulation of hydrogen ion dynamics that are driven by poor vascularity perfusion, regional hypoxia, and increased glycolysis. All these forces synergize/orchestrate together to create extracellular acidity and intracellular alkalinity. Precisely, they lead to extracellu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696090/ https://www.ncbi.nlm.nih.gov/pubmed/31357694 http://dx.doi.org/10.3390/ijms20153694 |
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author | Cardone, Rosa Angela Alfarouk, Khalid Omer Elliott, Robert L. Alqahtani, Saad Saeed Ahmed, Samrein B. M. Aljarbou, Ahmed N. Greco, Maria Raffaella Cannone, Stefania Reshkin, Stephan Joel |
author_facet | Cardone, Rosa Angela Alfarouk, Khalid Omer Elliott, Robert L. Alqahtani, Saad Saeed Ahmed, Samrein B. M. Aljarbou, Ahmed N. Greco, Maria Raffaella Cannone, Stefania Reshkin, Stephan Joel |
author_sort | Cardone, Rosa Angela |
collection | PubMed |
description | Cancer cells have an unusual regulation of hydrogen ion dynamics that are driven by poor vascularity perfusion, regional hypoxia, and increased glycolysis. All these forces synergize/orchestrate together to create extracellular acidity and intracellular alkalinity. Precisely, they lead to extracellular pH (pH(e)) values as low as 6.2 and intracellular pH values as high as 8. This unique pH gradient (∆pH(i) to ∆pH(e)) across the cell membrane increases as the tumor progresses, and is markedly displaced from the electrochemical equilibrium of protons. These unusual pH dynamics influence cancer cell biology, including proliferation, metastasis, and metabolic adaptation. Warburg metabolism with increased glycolysis, even in the presence of Oxygen with the subsequent reduction in Krebs’ cycle, is a common feature of most cancers. This metabolic reprogramming confers evolutionary advantages to cancer cells by enhancing their resistance to hypoxia, to chemotherapy or radiotherapy, allowing rapid production of biological building blocks that support cellular proliferation, and shielding against damaging mitochondrial free radicals. In this article, we highlight the interconnected roles of dysregulated pH dynamics in cancer initiation, progression, adaptation, and in determining the programming and re-programming of tumor cell metabolism. |
format | Online Article Text |
id | pubmed-6696090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66960902019-09-05 The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela Cardone, Rosa Angela Alfarouk, Khalid Omer Elliott, Robert L. Alqahtani, Saad Saeed Ahmed, Samrein B. M. Aljarbou, Ahmed N. Greco, Maria Raffaella Cannone, Stefania Reshkin, Stephan Joel Int J Mol Sci Review Cancer cells have an unusual regulation of hydrogen ion dynamics that are driven by poor vascularity perfusion, regional hypoxia, and increased glycolysis. All these forces synergize/orchestrate together to create extracellular acidity and intracellular alkalinity. Precisely, they lead to extracellular pH (pH(e)) values as low as 6.2 and intracellular pH values as high as 8. This unique pH gradient (∆pH(i) to ∆pH(e)) across the cell membrane increases as the tumor progresses, and is markedly displaced from the electrochemical equilibrium of protons. These unusual pH dynamics influence cancer cell biology, including proliferation, metastasis, and metabolic adaptation. Warburg metabolism with increased glycolysis, even in the presence of Oxygen with the subsequent reduction in Krebs’ cycle, is a common feature of most cancers. This metabolic reprogramming confers evolutionary advantages to cancer cells by enhancing their resistance to hypoxia, to chemotherapy or radiotherapy, allowing rapid production of biological building blocks that support cellular proliferation, and shielding against damaging mitochondrial free radicals. In this article, we highlight the interconnected roles of dysregulated pH dynamics in cancer initiation, progression, adaptation, and in determining the programming and re-programming of tumor cell metabolism. MDPI 2019-07-28 /pmc/articles/PMC6696090/ /pubmed/31357694 http://dx.doi.org/10.3390/ijms20153694 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Cardone, Rosa Angela Alfarouk, Khalid Omer Elliott, Robert L. Alqahtani, Saad Saeed Ahmed, Samrein B. M. Aljarbou, Ahmed N. Greco, Maria Raffaella Cannone, Stefania Reshkin, Stephan Joel The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title | The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title_full | The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title_fullStr | The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title_full_unstemmed | The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title_short | The Role of Sodium Hydrogen Exchanger 1 in Dysregulation of Proton Dynamics and Reprogramming of Cancer Metabolism as a Sequela |
title_sort | role of sodium hydrogen exchanger 1 in dysregulation of proton dynamics and reprogramming of cancer metabolism as a sequela |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696090/ https://www.ncbi.nlm.nih.gov/pubmed/31357694 http://dx.doi.org/10.3390/ijms20153694 |
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