摘要
癌症是一种多因素疾病,其发生和发展非常复杂。抗癌药物开发中最大的问题是获得多药耐药性和复发。传统的化学疗法直接针对细胞的DNA,而当代的抗癌药物则涉及分子靶向治疗,如靶向癌细胞内具有异常表达的蛋白质。传统的彻底根除癌细胞的策略被证明是无效的。靶向化疗在某些恶性肿瘤中取得了成功,但其效果往往受到耐药性和对正常组织和细胞副作用的限制。自从最近几年以来,已经确定了许多有前途的药物靶标用于有效治疗癌症。目前的综述文章描述了一些有希望的抗癌靶点,包括激酶,微管蛋白,癌症干细胞,单克隆抗体和血管靶向剂。另外,还描述了在临床试验的各个阶段有希望的候选药物。同时靶向不同癌细胞信号传导途径的多作用药物可促进有效的抗癌药物开发过程。
关键词: 抗癌剂,微管蛋白抑制剂,激酶,癌症干细胞,多药耐药性,多靶向药物。
Current Medicinal Chemistry
Title:Promising Targets in Anti-cancer Drug Development: Recent Updates
Volume: 24 Issue: 42
关键词: 抗癌剂,微管蛋白抑制剂,激酶,癌症干细胞,多药耐药性,多靶向药物。
摘要: Cancer is a multifactorial disease and its genesis and progression are extremely complex. The biggest problem in the anticancer drug development is acquiring of multidrug resistance and relapse. Classical chemotherapeutics directly target the DNA of the cell, while the contemporary anticancer drugs involve molecular-targeted therapy such as targeting the proteins possessing abnormal expression inside the cancer cells. Conventional strategies for the complete eradication of the cancer cells proved ineffective. Targeted chemotherapy was successful in certain malignancies however, the effectiveness has often been limited by drug resistance and side effects on normal tissues and cells. Since last few years, many promising drug targets have been identified for the effective treatment of cancer. The current review article describes some of these promising anticancer targets that include kinases, tubulin, cancer stem cells, monoclonal antibodies and vascular targeting agents. In addition, promising drug candidates under various phases of clinical trials are also described. Multi-acting drugs that simultaneously target different cancer cell signaling pathways may facilitate the process of effective anti-cancer drug development.
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Promising Targets in Anti-cancer Drug Development: Recent Updates, Current Medicinal Chemistry 2017; 24 (42) . https://dx.doi.org/10.2174/0929867324666170331123648
DOI https://dx.doi.org/10.2174/0929867324666170331123648 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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