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An update on anticancer drug development and delivery targeting carbonic anhydrase IX

机译:针对碳酸酐酶IX的抗癌药物开发和交付的最新信息

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摘要

The expression of carbonic anhydrase (CA) IX is up-regulated in many types of solid tumors in humans under hypoxic and acidic microenvironment. Inhibition of CA IX enzymatic activity with selective inhibitors, antibodies or labeled probes has been shown to reverse the acidic environment of solid tumors and reduce the tumor growth establishing the significant role of CA IX in tumorigenesis. Thus, the development of potent antitumor drugs targeting CA IX with minimal toxic effects is important for the target-specific tumor therapy. Recently, several promising antitumor agents against CA IX have been developed to treat certain types of cancers in combination with radiation and chemotherapy. Here we review the inhibition of CA IX by small molecule compounds and monoclonal antibodies. The methods of enzymatic assays, biophysical methods, animal models including zebrafish and Xenopus oocytes, and techniques of diagnostic imaging to detect hypoxic tumors using CA IX-targeted conjugates are discussed with the aim to overview the recent progress related to novel therapeutic agents that target CA IX in hypoxic tumors.
机译:在缺氧和酸性微环境下,人体中许多类型的实体瘤中碳酸酐酶(CA)IX的表达均上调。已经证明用选择性抑制剂,抗体或标记的探针抑制CA IX的酶促活性可以逆转实体瘤的酸性环境并减少肿瘤的生长,从而确立了CA IX在肿瘤发生中的重要作用。因此,开发针对CA IX的具有最小毒性作用的有效抗肿瘤药物对于靶标特异性肿瘤治疗很重要。最近,已经开发了几种针对CA IX的有前途的抗肿瘤药,以结合放射和化学疗法治疗某些类型的癌症。在这里,我们综述了小分子化合物和单克隆抗体对CA IX的抑制作用。讨论了酶促测定的方法,生物物理方法,包括斑马鱼和非洲爪蟾卵母细胞的动物模型以及使用CA IX靶向缀合物的诊断成像技术检测缺氧肿瘤的技术,目的是概述与靶向CA的新型治疗剂相关的最新进展IX在缺氧性肿瘤中。

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