| Literature DB >> 27823879 |
Simon J A van Kuijk1, Nanda Kumar Parvathaneni2, Raymon Niemans3, Marike W van Gisbergen3, Fabrizio Carta4, Daniela Vullo5, Silvia Pastorekova6, Ala Yaromina3, Claudiu T Supuran4, Ludwig J Dubois3, Jean-Yves Winum7, Philippe Lambin3.
Abstract
Carbonic anhydrase IX (CAIX) is a hypoxia-regulated and tumor-specific protein that maintains the pH balance of cells. Targeting CAIX might be a valuable approach for specific delivery of cytotoxic drugs, thereby reducing normal tissue side-effects. A series of dual-target compounds were designed and synthesized incorporating a sulfonamide, sulfamide, or sulfamate moiety combined with several different anti-cancer drugs, including the chemotherapeutic agents chlorambucil, tirapazamine, and temozolomide, two Ataxia Telangiectasia and Rad3-related protein inhibitors (ATRi), and the anti-diabetic biguanide agent phenformin. An ATRi derivative (12) was the only compound to show a preferred efficacy in CAIX overexpressing cells versus cells without CAIX expression when combined with radiation. Its efficacy might however not solely depend on binding to CAIX, since all described compounds generally display low activity as carbonic anhydrase inhibitors. The hypothesis that dual-target compounds specifically target CAIX expressing tumor cells was therefore not confirmed. Even though dual-target compounds remain an interesting approach, alternative options should also be investigated as novel treatment strategies.Entities:
Keywords: CAIX inhibitors; Carbonic anhydrase IX; Cytotoxic drugs; Dual-target drugs; Hypoxia; Tumor
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Year: 2016 PMID: 27823879 DOI: 10.1016/j.ejmech.2016.10.037
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514