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靶向碳酸酐酶IX的抗癌药物研发与递送进展

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

作者信息

Kazokaitė Justina, Aspatwar Ashok, Parkkila Seppo, Matulis Daumantas

机构信息

Department of Biothermodynamics and Drug Design, Institute of Biotechnology, Vilnius University, Vilnius, Lithuania.

Faculty of Medicine and Life sciences, University of Tampere, Tampere, Finland.

出版信息

PeerJ. 2017 Nov 23;5:e4068. doi: 10.7717/peerj.4068. eCollection 2017.

Abstract

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 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.

摘要

在缺氧和酸性微环境下,碳酸酐酶(CA)IX在人类多种实体瘤中的表达上调。使用选择性抑制剂、抗体或标记探针抑制CA IX的酶活性已被证明可逆转实体瘤的酸性环境并减少肿瘤生长,这确立了CA IX在肿瘤发生中的重要作用。因此,开发具有最小毒性作用的靶向CA IX的强效抗肿瘤药物对于靶向特异性肿瘤治疗很重要。最近,已经开发了几种有前景的抗CA IX抗肿瘤药物,用于与放疗和化疗联合治疗某些类型的癌症。在此,我们综述小分子化合物和单克隆抗体对CA IX的抑制作用。讨论了酶促测定方法、生物物理方法、包括斑马鱼和卵母细胞在内的动物模型,以及使用CA IX靶向缀合物检测缺氧肿瘤的诊断成像技术,旨在概述与靶向缺氧肿瘤中CA IX的新型治疗药物相关的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e306/5702504/9419f84e4dc0/peerj-05-4068-g001.jpg

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