吴增丁 (2022-06-30 16:51):
#paper . doi:10.1038/s41392-021-00572-w 分享一篇发表在2021年nature子刊Signal Transduction and Targeted Therapy的有关肿瘤靶向治疗小分子药物研发的综述:Small molecules in targeted cancer therapy: advances, challenges, and future perspectives. Signal Transduction and Targeted Therapy。 这篇文章汇总了自2001年第一个靶向治疗药物伊马替尼(格列卫--我不是药神)上市以来二十年间89种抗肿瘤小分子药,其对应的靶点涵盖了酪受体氨酸激酶抑制剂(ALK/c-MET/EGFR/FLT3/VEGFR/FGFR/PDGFR/NTRK)、非受体酪氨酸激酶抑制剂(BCR-ABL/BTK/JAK)、丝氨酸/苏氨酸激酶抑制剂(BRAF/MEK/ERK/CDK/PI3K/AKT/mTOR)、酪氨酸激酶样激酶抑制剂(BRAF/MEK/ERK/CDK/PI3K/AKT/mTOR)、 表观遗传抑制剂(EZH/HDAC/IDH1,2)、BCL-2 抑制剂、PROTEASOME 抑制剂、以及合成致死(PARP)。这些靶点中酪氨酸激酶获批的药物最多。本文章并没有太多新颖之处,主要是以量取胜,几乎每一种药物都有相关内容的阐述,所以工作量还是蛮大的。这篇文章适合当做字典对靶向药的查询使用。
Small molecules in targeted cancer therapy: advances, challenges, and future perspectives
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Abstract:
Due to the advantages in efficacy and safety compared with traditional chemotherapy drugs, targeted therapeutic drugs have become mainstream cancer treatments. Since the first tyrosine kinase inhibitor imatinib was approved to enter the market by the US Food and Drug Administration (FDA) in 2001, an increasing number of small-molecule targeted drugs have been developed for the treatment of malignancies. By December 2020, 89 small-molecule targeted antitumor drugs have been approved by the US FDA and the National Medical Products Administration (NMPA) of China. Despite great progress, small-molecule targeted anti-cancer drugs still face many challenges, such as a low response rate and drug resistance. To better promote the development of targeted anti-cancer drugs, we conducted a comprehensive review of small-molecule targeted anti-cancer drugs according to the target classification. We present all the approved drugs as well as important drug candidates in clinical trials for each target, discuss the current challenges, and provide insights and perspectives for the research and development of anti-cancer drugs.
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