在瘤条件下,关于小分子VEGFR抑制剂的最新进展和未来方向
Amandeep Thakur1, Mandeep Rana1, Anshul Mishra1
1School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei 110031, Taiwan.
European journal of medicinal chemistry
|May 10, 2024
概括
血管内皮生长因子受体 (VEGFR) 抑制剂在癌症治疗中表现有前途,但面临挑战. 本综述探讨了它们的发展,局限性和改善它们对各种恶性瘤的临床应用的策略.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 药物发现 药物发现 药物发现
背景情况:
- 血管内皮生长因子受体 (VEGFR) 抑制剂已经成为癌症治疗中的关键抗血管原体疗法.
- 尽管获得FDA批准,但其临床应用受到并发症和有效性有限的阻碍.
- 目前正在进行的研究重点是提高VEGFR抑制剂从临床前到临床阶段的转化.
研究的目的:
- 在过去十年中,审查VEGFR抑制剂作为癌症治疗药物的进展.
- 分析VEGFR的结构和分子特性,以及生理功能.
- 讨论限制VEGFR抑制剂活性和临床适用性的障碍,并提出克服这些障碍的策略.
主要方法:
- 在癌症治疗中对VEGFR抑制剂的综合文献综述.
- 分析VEGFR的结构/分子特性和生理功能.
- 检查FDA批准的VEGFR抑制剂及其局限性.
- 讨论提高VEGFR抑制剂的疗效和临床应用的策略.
主要成果:
- VEGFR 抑制剂代表着日益增长的一类具有显著治疗潜力的抗血管性疗法.
- 设计了多种结构组合,以利用VEGFR抑制剂的抗增殖潜力.
- 关键障碍包括抵抗机制,毒性和非目标效应,限制它们的活动范围.
结论:
- 在现代瘤学中,VEGFR抑制剂至关重要,但克服它们的局限性对于更广泛的临床成功至关重要.
- 战略设计和组合疗法对于提高VEGFR抑制剂的疗效至关重要.
- 本综述为推进基于VEGFR抑制剂的癌症治疗进入进一步的临床研究提供了见解.
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