配体靶向药物偶联物治疗癌症的体内评价

Q3 Biochemistry, Genetics and Molecular Biology Current protocols in chemical biology Pub Date : 2018-09-13 DOI:10.1002/cpch.49
Mena Asha Krishnan, Amit Pandit, Venkatesh Chelvam
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引用次数: 1

摘要

小分子配体靶向疗法的发展目前对癌症的治疗至关重要,因为它们有可能降低系统毒性并增加化疗药物的效力。靶向给药技术的主要目的是选择性地将药物货物释放到肿瘤组织中,避免化疗期间对健康组织和器官的非现场毒性。在这种策略中,化疗药物通过肽连接剂和促进药物在细胞内释放的自焚片段,结合到对癌细胞上过度表达的蛋白质具有高亲和力的归巢配体上。在靶向药物偶联物的开发过程中,在小鼠等小动物肿瘤模型中的临床前评估为药物的临床性能提供了有价值的数据。本文介绍了一套肿瘤植入方案,确定有效治疗所需的最佳剂量,以及估计癌症治疗期间小鼠肿瘤模型中任何可见副作用所需的最大耐受剂量。©2018 by John Wiley &儿子,Inc。
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In Vivo Evaluation of Ligand Targeted Drug Conjugates for Cancer Therapy

The development of small molecule ligand–targeted therapeutics is currently of paramount importance for treatment of cancer due to their potential to reduce system toxicity and increase potency of a delivered chemotherapeutic drug. The main aim of a targeted drug-delivery technique is to release the drug cargo selectively into tumor tissues, avoiding off-site toxicity to healthy tissues and organs during chemotherapy. In this strategy, a chemotherapeutic drug is conjugated to a homing ligand, which has high affinity for proteins over-expressed on cancer cells, via a peptide linker and a self-immolative segment that facilitates intracellular release of drug cargo. During development of targeted drug conjugates, preclinical evaluation in tumor models of small animals like mice adds valuable data on the clinical performance of the drug. This article contains a set of protocols for implantation of tumor, determination of optimum dosage required for effective treatment, and estimation of maximum tolerated dose required for any visible side effects during treatment of cancer in tumor models of mice. © 2018 by John Wiley & Sons, Inc.

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Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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