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第四代表皮生长因子受体抑制剂在克服 C797S 突变方面的药用化学新机遇。

The new opportunities in medicinal chemistry of fourth-generation EGFR inhibitors to overcome C797S mutation.

机构信息

Jiangxi Provincial Key Laboratory of Drug Design and Evaluation, School of Pharmacy, Jiangxi Science & Technology Normal University, 605 Fenglin Road, Nanchang, Jiangxi, 330013, China.

College of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang, 330004, China.

出版信息

Eur J Med Chem. 2021 Jan 15;210:112995. doi: 10.1016/j.ejmech.2020.112995. Epub 2020 Nov 16.

Abstract

Epidermal growth factor receptor (EGFR) is a receptor for epithelial growth factor (EGF) cell proliferation and signaling, which is related to the inhibition of tumor cell proliferation, angiogenesis, tumor invasion, metastasis, and apoptosis. Thus, it has become an important target for the treatment of non-small cell lung cancer (NSCLC). The first to the third-generation EGFR inhibitors have demonstrated powerful efficacy and brought a prospect to patients. Unfortunately, after 9-15 months of treatment, they all developed resistance without exception. As for the resistance of third-generation inhibitors, no major breakthrough has been made in this field. In this review, we discussed the recent advances in medicinal chemistry of fourth-generation EGFR-TKIs, as well as further discussed the clinical challenges and future prospects of treating patients with EGFR mutations resistant to third-generation EGFR-TKIs.

摘要

表皮生长因子受体(EGFR)是表皮生长因子(EGF)的细胞增殖和信号转导受体,与抑制肿瘤细胞增殖、血管生成、肿瘤侵袭、转移和凋亡有关。因此,它已成为治疗非小细胞肺癌(NSCLC)的重要靶点。第一代至第三代 EGFR 抑制剂已显示出强大的疗效,为患者带来了希望。不幸的是,在治疗 9-15 个月后,它们无一例外地都产生了耐药性。至于第三代抑制剂的耐药性,在这一领域还没有取得重大突破。在这篇综述中,我们讨论了第四代 EGFR-TKIs 的药物化学最新进展,并进一步讨论了治疗第三代 EGFR-TKIs 耐药 EGFR 突变患者的临床挑战和未来前景。

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