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Article Publish Status: FREE
Abstract Title:

Bicarbonate increases tumor pH and inhibits spontaneous metastases.

Abstract Source:

Cancer Res. 2009 Mar 15 ;69(6):2260-8. Epub 2009 Mar 10. PMID: 19276390

Abstract Author(s):

Ian F Robey, Brenda K Baggett, Nathaniel D Kirkpatrick, Denise J Roe, Julie Dosescu, Bonnie F Sloane, Arig Ibrahim Hashim, David L Morse, Natarajan Raghunand, Robert A Gatenby, Robert J Gillies

Article Affiliation:

Arizona Cancer Center, University of Arizona, Tucson, Arizona, USA.

Abstract:

The external pH of solid tumors is acidic as a consequence of increased metabolism of glucose and poor perfusion. Acid pH has been shown to stimulate tumor cell invasion and metastasis in vitro and in cells before tail vein injection in vivo. The present study investigates whether inhibition of this tumor acidity will reduce the incidence of in vivo metastases. Here, we show that oral NaHCO(3) selectively increased the pH of tumors and reduced the formation of spontaneous metastases in mouse models of metastatic breast cancer. This treatment regimen was shown to significantly increase the extracellular pH, but not the intracellular pH, of tumors by (31)P magnetic resonance spectroscopy and the export of acid from growing tumors by fluorescence microscopy of tumors grown in window chambers. NaHCO(3) therapy also reduced the rate of lymph node involvement, yet did not affect the levels of circulating tumor cells, suggesting that reduced organ metastases were not due to increased intravasation. In contrast, NaHCO(3) therapy significantly reduced the formation of hepatic metastases following intrasplenic injection, suggesting that it did inhibit extravasation and colonization. In tail vein injections of alternative cancer models, bicarbonate had mixed results, inhibiting the formation of metastases from PC3M prostate cancer cells, but not those of B16 melanoma. Although the mechanism of this therapy is not known with certainty, low pH was shown to increase the release of active cathepsin B, an important matrix remodeling protease.

Study Type : Animal Study

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Sayer Ji
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