Mechanisms of buffer therapy resistance

Autor: Yoganand Balagurunathan, Jonathan W. Wojtkowiak, Maria de Lourdes Coelho Ribeiro, Heather H. Cornnell, Robert J. Gillies, Kate M. Bailey, Arig Ibrahim Hashim
Rok vydání: 2014
Předmět:
Zdroj: Neoplasia: An International Journal for Oncology Research, Vol 16, Iss 4, Pp 354-364.e3 (2014)
ISSN: 1476-5586
DOI: 10.1016/j.neo.2014.04.005
Popis: Many studies have shown that the acidity of solid tumors contributes to local invasion and metastasis. Oral pH buffers can specifically neutralize the acidic pH of tumors and reduce the incidence of local invasion and metastatic formation in multiple murine models. However, this effect is not universal as we have previously observed that metastasis is not inhibited by buffers in some tumor models, regardless of buffer used. B16-F10 (murine melanoma), LL/2 (murine lung) and HCT116 (human colon) tumors are resistant to treatment with lysine buffer therapy, whereas metastasis is potently inhibited by lysine buffers in MDA-MB-231 (human breast) and PC3M (human prostate) tumors. In the current work, we confirmed that sensitive cells utilized a pH-dependent mechanism for successful metastasis supported by a highly glycolytic phenotype that acidifies the local tumor microenvironment resulting in morphological changes. In contrast, buffer-resistant cell lines exhibited a pH-independent metastatic mechanism involving constitutive secretion of matrix degrading proteases without elevated glycolysis. These results have identified two distinct mechanisms of experimental metastasis, one of which is pH-dependent (buffer therapy sensitive cells) and one which is pH-independent (buffer therapy resistant cells). Further characterization of these models has potential for therapeutic benefit.
Databáze: OpenAIRE
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