靶向C-Met的生物活性产品作为潜在的抗肿瘤药物。

IF 2.6 4区 医学 Q3 CHEMISTRY, MEDICINAL Anti-cancer agents in medicinal chemistry Pub Date : 2025-01-13 DOI:10.2174/0118715206346207241217064022
Liying Zhao, Chunmei Qian, Xiaoqi Ma, Xiaoyu Wang
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引用次数: 0

摘要

间充质上皮转化因子(c-Met)是一种受体酪氨酸激酶(RTK),在细胞增殖、迁移侵袭和肿瘤转移中起着至关重要的作用。目的:随着治疗时间的延长,许多肿瘤逐渐产生耐药性。因此,需要开发新的抗肿瘤药物来治疗肿瘤患者。靶向c-met抑制剂可能是一种有效的治疗策略。方法:利用ScienceDirect、PubMed、Wiley Online Library、Social Sciences Citation Index等科学数据库收集信息。对所有相关文献进行综述,并对现有文献进行筛选。根据文章标题、摘要和全文检索c-Met的上游和下游途径及其与抗肿瘤作用的相关性。现将具有抗肿瘤作用的c- met靶向药物总结如下。在筛选过程中使用了“引文中的引文”或滚雪球方法,以确定在最初的文献筛选过程中可能遗漏的其他论文。本综述对发表在同行评议期刊上的高质量研究进行了总结和优先引用。结果:近年来,小分子靶向药物的研究发展迅速。从天然化合物和中药中合成和分离c-Met抑制剂也取得了许多成果。结论:本文综述了从天然化合物和中药中合成和分离的抗c- met药物的研究进展。本研究为开发c-Met抑制剂提供了主要资源。
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Bioactive Products Targeting C-Met As Potential Antitumour Drugs.

Mesenchymal‒epithelial transition factor (c-Met), a receptortyrosine kinase (RTK), plays a vital role in cell proliferation, migration and invasion, and tumour metastasis.

Objective: With increasing duration of treatment, many tumours gradually develop drug resistance. Therefore, novel antitumour drugs need to be developed to treat patients with tumours. Targeting c-met inhibitors may be an effective treatment strategy.

Methods: Scientific databases such as ScienceDirect, PubMed, the Wiley Online Library, and Social Sciences Citation Index were used to collect information. All the relevant literature was reviewed, and the available literature was screened. The upstream and downstream pathways of c-Met and their relevance to antitumour effects were searched based on the articles' title, abstract, and full text. The c-Met-targeting drugs with antitumour effects are summarized below. A "citation within a citation" or snowballing approach was used in this screening process to identify additional papers that may have been missed in the initial literature screening process. High-quality studies published in peer-reviewed journals were summarized and prioritized for citation in the review.

Results: In recent years, research on small-molecule targeted drugs has developed rapidly. Many results have also been achieved in the synthesis and isolation of c-Met inhibitors from natural compounds and traditional Chinese medicines.

Conclusion: This article summarizes the developments in anti-c-Met drugs, which are synthesized and isolated from natural compounds and traditional Chinese medicine (TCM). This study provides primary resources for the development of c-Met inhibitors.

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来源期刊
Anti-cancer agents in medicinal chemistry
Anti-cancer agents in medicinal chemistry ONCOLOGY-CHEMISTRY, MEDICINAL
CiteScore
5.10
自引率
3.60%
发文量
323
审稿时长
4-8 weeks
期刊介绍: Formerly: Current Medicinal Chemistry - Anti-Cancer Agents. Anti-Cancer Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of anti-cancer agents. Each issue contains a series of timely in-depth reviews and guest edited issues written by leaders in the field covering a range of current topics in cancer medicinal chemistry. The journal only considers high quality research papers for publication. Anti-Cancer Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in cancer drug discovery.
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