Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer

<p>Abstract</p> <p>Background</p> <p>The glycolytic nature of malignant tumors contributes to high levels of extracellular acidity in the tumor microenvironment. Tumor acidity is a driving force in invasion and metastases. Recently, it has been shown that buffering of e...

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Main Authors: Martin Natasha K, Robey Ian F
Format: Article
Language:English
Published: BMC 2011-06-01
Series:BMC Cancer
Subjects:
pH
Online Access:http://www.biomedcentral.com/1471-2407/11/235
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spelling doaj-a77352f687f64ffb891a53518f6f39942020-11-25T02:18:57ZengBMCBMC Cancer1471-24072011-06-0111123510.1186/1471-2407-11-235Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancerMartin Natasha KRobey Ian F<p>Abstract</p> <p>Background</p> <p>The glycolytic nature of malignant tumors contributes to high levels of extracellular acidity in the tumor microenvironment. Tumor acidity is a driving force in invasion and metastases. Recently, it has been shown that buffering of extracellular acidity through systemic administration of oral bicarbonate can inhibit the spread of metastases in a mouse model for metastatic breast cancer. While these findings are compelling, recent assessments into the use of oral bicarbonate as a cancer intervention reveal limitations.</p> <p>Methods</p> <p>We posited that safety and efficacy of bicarbonate could be enhanced by dichloroacetate (DCA), a drug that selectively targets tumor cells and reduces extracellular acidity through inhibition of glycolysis. Using our mouse model for metastatic breast cancer (MDA-MB-231), we designed an interventional survival study where tumor bearing mice received bicarbonate, DCA, or DCA-bicarbonate (DB) therapies chronically.</p> <p>Results</p> <p>Dichloroacetate alone or in combination with bicarbonate did not increase systemic alkalosis in mice. Survival was longest in mice administered bicarbonate-based therapies. Primary tumor re-occurrence after surgeries is associated with survival rates. Although DB therapy did not significantly enhance oral bicarbonate, we did observe reduced pulmonary lesion diameters in this cohort. The DCA monotherapy was not effective in reducing tumor size or metastases or improving survival time. We provide <it>in vitro </it>evidence to suggest this outcome may be a function of hypoxia in the tumor microenvironment.</p> <p>Conclusions</p> <p>DB combination therapy did not appear to enhance the effect of chronic oral bicarbonate. The anti-tumor effect of DCA may be dependent on the cancer model. Our studies suggest DCA efficacy is unpredictable as a cancer therapy and further studies are necessary to determine the role of this agent in the tumor microenvironment.</p> http://www.biomedcentral.com/1471-2407/11/235TumorpHAcidityDichloroacetateSodium bicarbonate
collection DOAJ
language English
format Article
sources DOAJ
author Martin Natasha K
Robey Ian F
spellingShingle Martin Natasha K
Robey Ian F
Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
BMC Cancer
Tumor
pH
Acidity
Dichloroacetate
Sodium bicarbonate
author_facet Martin Natasha K
Robey Ian F
author_sort Martin Natasha K
title Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
title_short Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
title_full Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
title_fullStr Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
title_full_unstemmed Bicarbonate and dichloroacetate: Evaluating pH altering therapies in a mouse model for metastatic breast cancer
title_sort bicarbonate and dichloroacetate: evaluating ph altering therapies in a mouse model for metastatic breast cancer
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2011-06-01
description <p>Abstract</p> <p>Background</p> <p>The glycolytic nature of malignant tumors contributes to high levels of extracellular acidity in the tumor microenvironment. Tumor acidity is a driving force in invasion and metastases. Recently, it has been shown that buffering of extracellular acidity through systemic administration of oral bicarbonate can inhibit the spread of metastases in a mouse model for metastatic breast cancer. While these findings are compelling, recent assessments into the use of oral bicarbonate as a cancer intervention reveal limitations.</p> <p>Methods</p> <p>We posited that safety and efficacy of bicarbonate could be enhanced by dichloroacetate (DCA), a drug that selectively targets tumor cells and reduces extracellular acidity through inhibition of glycolysis. Using our mouse model for metastatic breast cancer (MDA-MB-231), we designed an interventional survival study where tumor bearing mice received bicarbonate, DCA, or DCA-bicarbonate (DB) therapies chronically.</p> <p>Results</p> <p>Dichloroacetate alone or in combination with bicarbonate did not increase systemic alkalosis in mice. Survival was longest in mice administered bicarbonate-based therapies. Primary tumor re-occurrence after surgeries is associated with survival rates. Although DB therapy did not significantly enhance oral bicarbonate, we did observe reduced pulmonary lesion diameters in this cohort. The DCA monotherapy was not effective in reducing tumor size or metastases or improving survival time. We provide <it>in vitro </it>evidence to suggest this outcome may be a function of hypoxia in the tumor microenvironment.</p> <p>Conclusions</p> <p>DB combination therapy did not appear to enhance the effect of chronic oral bicarbonate. The anti-tumor effect of DCA may be dependent on the cancer model. Our studies suggest DCA efficacy is unpredictable as a cancer therapy and further studies are necessary to determine the role of this agent in the tumor microenvironment.</p>
topic Tumor
pH
Acidity
Dichloroacetate
Sodium bicarbonate
url http://www.biomedcentral.com/1471-2407/11/235
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