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蛋白质激酶作为开发天然生物碱抗癌药物的治疗靶点。

Protein kinases as therapeutic targets to develop anticancer drugs with natural alkaloids.

作者信息

Ye Hanlin, Wang Linlin, Ma Li, Ionov Maksim, Qiao Gan, Huang Jianlin, Cheng Li, Zhang Yuxi, Yang Xiaohui, Cao Shousong, Lin Xiukun

机构信息

Department of Pharmacology, School of Pharmacy, Southwest Medical University, 646000 Luzhou, Sichuan, China.

Rizhao Hospital of Traditional Chinese Medicine, 276826 Rizhao, Shandong, China.

出版信息

Front Biosci (Landmark Ed). 2021 Nov 30;26(11):1349-1361. doi: 10.52586/5028.

DOI:10.52586/5028
PMID:34856772
Abstract

: Protein kinases play an important role in cell proliferation, differentiation, mobility and cell cycle arrest etc. These enzymes act as important targets in developing anticancer agents. Over the years, a large number of protein kinase inhibitors have been discovered and developed as anticancer agents for the treatment of cancers clinically. However, the drug-resiatance and off-targeting limit their effeciancy for the treatment of human cancer. : Alkaloids are an important class of natural products with broad spectrum biological activities. In the past decades, numerus alkaloids with significant anticancer activity by inhibiting protein kinases were identified. In the present mini-review, we will present the key enzymes including mitogen-activated protein kinase (MAPK), phosphoinositide 3-kinase/protein kinase B/mammalian target of rapamycin (PI3K/AKT/mTOR) and janus-activated kinases/signal transducer and activator of transcription (JAK/STAT) targeted by alkaloids and highlight the special sites targeted by alkaloids on protein kinases and/or reversing drug resistance. Additionally, the challenge and prospect of developing alkaloids as new anticancer agents are also discussed. : Alkaloids suppressed tumor growth through targeting different signaling pathways mediated by protein kinases of cancer cells. It is conceivable that novel alkaloids anticancer agents with promising clinical value will be developed in the future.

摘要

蛋白激酶在细胞增殖、分化、迁移和细胞周期阻滞等过程中发挥着重要作用。这些酶是开发抗癌药物的重要靶点。多年来,大量蛋白激酶抑制剂已被发现并开发为临床治疗癌症的抗癌药物。然而,耐药性和脱靶效应限制了它们治疗人类癌症的效果。

生物碱是一类具有广泛生物活性的重要天然产物。在过去几十年中,人们鉴定出了许多通过抑制蛋白激酶具有显著抗癌活性的生物碱。在本综述中,我们将介绍生物碱作用的关键酶,包括丝裂原活化蛋白激酶(MAPK)、磷酸肌醇3激酶/蛋白激酶B/雷帕霉素哺乳动物靶蛋白(PI3K/AKT/mTOR)和Janus激酶/信号转导子和转录激活子(JAK/STAT),并突出生物碱在蛋白激酶上作用的特殊位点和/或逆转耐药性的情况。此外,还讨论了将生物碱开发为新型抗癌药物面临的挑战和前景。

生物碱通过作用于癌细胞蛋白激酶介导的不同信号通路来抑制肿瘤生长。可以想象,未来将会开发出具有良好临床价值的新型生物碱抗癌药物。

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