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首页> 外文期刊>Recent patents on anti-cancer drug discovery >Recent developments in patent anti-cancer agents targeting the matrix metalloproteinases (MMPs).
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Recent developments in patent anti-cancer agents targeting the matrix metalloproteinases (MMPs).

机译:靶向基质金属蛋白酶(MMP)的专利抗癌药的最新进展。

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Matrix metalloproteinases (MMPs) belong to a family of closely related calcium- and zinc-dependent endopeptidases involved in the degradation and remodeling of extracellular matrix (ECM) proteins that are associated with the tumorigenic processes. MMPs promote tumor invasion and metastasis, regulating host defense mechanisms and normal cell function. Thus, MMP inhibitors (MMPIs) are expected to be useful chemotherapeutic agents for the treatment of malignant cancer, osteoarthritis, and rheumatoid arthritis. A vast number of small molecular MMPIs have been developed in recent years. Although there have been considerable preclinical and clinical studies on these inhibitors, most of the effective candidates in clinical trials, however, have yielded unsatisfactory results, thus they are as yet unavailable for use as therapeutic drugs. Currently, more efforts have been directed to the design of specific inhibitors towards certain MMP family members for selective usage. This review will focus primarily on an analysis of recent developed MMPIs that have entered preclinical or clinical trials, and recently registered patents with regard to new highly selective MMPIs in USA or patent applications related to the specific inhibitors of MMPs. We also analyze the clinical failure and discuss the possible strategies to best optimize the development of these novel agents.
机译:基质金属蛋白酶(MMP)属于紧密相关的钙和锌依赖性内肽酶家族,参与与致瘤过程相关的细胞外基质(ECM)蛋白的降解和重塑。 MMP促进肿瘤的侵袭和转移,调节宿主防御机制和正常细胞功能。因此,预期MMP抑制剂(MMPI)是用于治疗恶性癌症,骨关节炎和类风湿关节炎的化学治疗剂。近年来已经开发了许多小分子MMPI。尽管已经对这些抑制剂进行了大量的临床前和临床研究,但是,大多数有效的候选药物在临床试验中均未获得令人满意的结果,因此尚不能用作治疗药物。当前,针对特定MMP家族成员的选择性抑制剂的设计已经进行了更多的努力,以供选择性使用。这篇综述将主要侧重于对已进入临床前或临床试验的最新开发的MMPI进行分析,以及最近在美国注册的有关新型高选择性MMPI的专利或与MMP特定抑制剂有关的专利申请。我们还将分析临床失败并讨论可能的策略,以最佳地优化这些新型药物的开发。

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