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小分子 Tubulysin B 缀合物的开发用于治疗表达碳酸酐酶 IX 受体的癌症。

Development of a Small Molecule Tubulysin B Conjugate for Treatment of Carbonic Anhydrase IX Receptor Expressing Cancers.

机构信息

On Target Laboratories , West Lafayette , Indiana 47907 , United States.

出版信息

Mol Pharm. 2018 Jun 4;15(6):2289-2296. doi: 10.1021/acs.molpharmaceut.8b00139. Epub 2018 May 1.

Abstract

Carbonic anhydrase IX (CAIX) is a membrane-spanning zinc metalloenzyme that catalyzes the reversible consumption of CO and water to form H + HCO. Many human cancers upregulate CAIX to help control the pH in their hypoxic microenvironments. The consequent overexpression of CAIX on malignant cells and low expression on normal tissues render CAIX a particularly attractive target for small molecule inhibitors, antibody-drug conjugates, and ligand-targeted drugs. In this study, CAIX-targeted fluorescent reporter molecules were initially exploited to investigate CAIX-specific binding to multiple cancer cell lines, where they were shown to display potent and selective binding to CAIX positive cells. A small molecule CAIX-targeted tubulysin B conjugate was then synthesized and examined for its ability to kill CAIX-expressing tumor cells in vitro. Potent therapeutic conjugates were subsequently tested in vivo and demonstrated to eliminate solid human tumor xenografts in murine tumor models without exhibiting overt signs of toxicity. Because most solid tumors contain hypoxic regions where CAIX is overexpressed, development of a method to selectively deliver drugs to these hypoxic regions could aid in the therapy of otherwise difficult to treat tumors.

摘要

碳酸酐酶 IX(CAIX)是一种跨膜锌金属酶,可催化 CO 和水的可逆消耗,形成 H + HCO。许多人类癌症上调 CAIX 以帮助控制其缺氧微环境中的 pH 值。恶性细胞中 CAIX 的过度表达和正常组织中的低表达使 CAIX 成为小分子抑制剂、抗体药物偶联物和配体靶向药物的特别有吸引力的靶标。在这项研究中,最初利用 CAIX 靶向荧光报告分子来研究 CAIX 与多种癌细胞系的特异性结合,结果表明它们对 CAIX 阳性细胞表现出强大且选择性的结合。然后合成了一种小分子 CAIX 靶向微管蛋白 B 缀合物,并研究了其在体外杀死 CAIX 表达肿瘤细胞的能力。随后在体内测试了有效的治疗性缀合物,在没有表现出明显毒性迹象的情况下,消除了小鼠肿瘤模型中的人实体瘤异种移植物。由于大多数实体瘤含有缺氧区域,其中 CAIX 过表达,因此开发一种选择性将药物递送至这些缺氧区域的方法可能有助于治疗其他难以治疗的肿瘤。

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