Targeting Hypoxic Tumor Cell Viability with Carbohydrate-Based Carbonic Anhydrase IX and XII Inhibitors

Jason C. Morris(Griffith University), Johanna Chiche(Centre National de la Recherche Scientifique), Caroline Grellier(Griffith University), Marie Lopez(Griffith University), Laurent F. Bornaghi(Griffith University), Alfonso Maresca(University of Florence), Claudiu T. Supuran(University of Florence), Jacques Pouysségur(Centre National de la Recherche Scientifique), Sally‐Ann Poulsen(Griffith University)
Journal of Medicinal Chemistry
August 18, 2011
Cited by 123Open Access
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Abstract

Carbonic anhydrase (CA) enzymes, specifically membrane-bound isozymes CA IX and CA XII, underpin a pH-regulating system that enables hypoxic tumor cell survival and proliferation. CA IX and XII are implicated as potential targets for the development of new hypoxic cancer therapies. To date, only a few small molecules have been characterized in CA-relevant cell and animal model systems. In this paper, we describe the development of a new class of carbohydrate-based small molecule CA inhibitors, many of which inhibit CA IX and XII within a narrow range of low nanomolar K(i) values (5.3-11.2 nM). We evaluate for the first time carbohydrate-based CA inhibitors in cell-based models that emulate the protective role of CA IX in an acidic tumor microenvironment. Our findings identified two inhibitors (compounds 5 and 17) that block CA IX-induced survival and have potential for development as in vivo cancer cell selective inhibitors.


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