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Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis
The rapid growth of cancer cells fueled by glycolysis produces large amounts of protons in cancer cells, which tri mechanisms to transport them out, hence leading to increased acidity in their extracellular environments. It has been well established that the increased acidity will induce cell death...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743895/ https://www.ncbi.nlm.nih.gov/pubmed/23967163 http://dx.doi.org/10.1371/journal.pone.0071177 |
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author | Xu, Kun Mao, Xizeng Mehta, Minesh Cui, Juan Zhang, Chi Mao, Fenglou Xu, Ying |
author_facet | Xu, Kun Mao, Xizeng Mehta, Minesh Cui, Juan Zhang, Chi Mao, Fenglou Xu, Ying |
author_sort | Xu, Kun |
collection | PubMed |
description | The rapid growth of cancer cells fueled by glycolysis produces large amounts of protons in cancer cells, which tri mechanisms to transport them out, hence leading to increased acidity in their extracellular environments. It has been well established that the increased acidity will induce cell death of normal cells but not cancer cells. The main question we address here is: how cancer cells deal with the increased acidity to avoid the activation of apoptosis. We have carried out a comparative analysis of transcriptomic data of six solid cancer types, breast, colon, liver, two lung (adenocarcinoma, squamous cell carcinoma) and prostate cancers, and proposed a model of how cancer cells utilize a few mechanisms to keep the protons outside of the cells. The model consists of a number of previously, well or partially, studied mechanisms for transporting out the excess protons, such as through the monocarboxylate transporters, V-ATPases, NHEs and the one facilitated by carbonic anhydrases. In addition we propose a new mechanism that neutralizes protons through the conversion of glutamate to γ-aminobutyrate, which consumes one proton per reaction. We hypothesize that these processes are regulated by cancer related conditions such as hypoxia and growth factors and by the pH levels, making these encoded processes not available to normal cells under acidic conditions. |
format | Online Article Text |
id | pubmed-3743895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37438952013-08-21 Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis Xu, Kun Mao, Xizeng Mehta, Minesh Cui, Juan Zhang, Chi Mao, Fenglou Xu, Ying PLoS One Research Article The rapid growth of cancer cells fueled by glycolysis produces large amounts of protons in cancer cells, which tri mechanisms to transport them out, hence leading to increased acidity in their extracellular environments. It has been well established that the increased acidity will induce cell death of normal cells but not cancer cells. The main question we address here is: how cancer cells deal with the increased acidity to avoid the activation of apoptosis. We have carried out a comparative analysis of transcriptomic data of six solid cancer types, breast, colon, liver, two lung (adenocarcinoma, squamous cell carcinoma) and prostate cancers, and proposed a model of how cancer cells utilize a few mechanisms to keep the protons outside of the cells. The model consists of a number of previously, well or partially, studied mechanisms for transporting out the excess protons, such as through the monocarboxylate transporters, V-ATPases, NHEs and the one facilitated by carbonic anhydrases. In addition we propose a new mechanism that neutralizes protons through the conversion of glutamate to γ-aminobutyrate, which consumes one proton per reaction. We hypothesize that these processes are regulated by cancer related conditions such as hypoxia and growth factors and by the pH levels, making these encoded processes not available to normal cells under acidic conditions. Public Library of Science 2013-08-14 /pmc/articles/PMC3743895/ /pubmed/23967163 http://dx.doi.org/10.1371/journal.pone.0071177 Text en © 2013 XU 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 Xu, Kun Mao, Xizeng Mehta, Minesh Cui, Juan Zhang, Chi Mao, Fenglou Xu, Ying Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title | Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title_full | Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title_fullStr | Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title_full_unstemmed | Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title_short | Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis |
title_sort | elucidation of how cancer cells avoid acidosis through comparative transcriptomic data analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743895/ https://www.ncbi.nlm.nih.gov/pubmed/23967163 http://dx.doi.org/10.1371/journal.pone.0071177 |
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