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肽类疗法:探索抗癌潜力——穿越1989年的历程

Peptide Therapeutics: Unveiling the Potential against Cancer-A Journey through 1989.

作者信息

Al Musaimi Othman

机构信息

School of Pharmacy, Faculty of Medical Sciences, Newcastle upon Tyne NE1 7RU, UK.

Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK.

出版信息

Cancers (Basel). 2024 Mar 2;16(5):1032. doi: 10.3390/cancers16051032.

Abstract

The United States Food and Drug Administration (FDA) has approved a plethora of peptide-based drugs as effective drugs in cancer therapy. Peptides possess high specificity, permeability, target engagement, and a tolerable safety profile. They exhibit selective binding with cell surface receptors and proteins, functioning as agonists or antagonists. They also serve as imaging agents for diagnostic applications or can serve a dual-purpose as both diagnostic and therapeutic (theragnostic) agents. Therefore, they have been exploited in various forms, including linkers, peptide conjugates, and payloads. In this review, the FDA-approved prostate-specific membrane antigen (PSMA) peptide antagonists, peptide receptor radionuclide therapy (PRRT), somatostatin analogs, antibody-drug conjugates (ADCs), gonadotropin-releasing hormone (GnRH) analogs, and other peptide-based anticancer drugs are analyzed in terms of their chemical structures and properties, therapeutic targets and mechanisms of action, development journey, administration routes, and side effects.

摘要

美国食品药品监督管理局(FDA)已批准大量基于肽的药物作为癌症治疗的有效药物。肽具有高特异性、渗透性、靶点亲和力和可耐受的安全性。它们与细胞表面受体和蛋白质表现出选择性结合,充当激动剂或拮抗剂。它们还用作诊断应用的成像剂,或可兼具诊断和治疗(诊疗)双重功能。因此,它们已被开发成各种形式,包括连接体、肽缀合物和有效载荷。在本综述中,将从化学结构和性质、治疗靶点和作用机制、研发历程、给药途径及副作用等方面,对FDA批准的前列腺特异性膜抗原(PSMA)肽拮抗剂、肽受体放射性核素治疗(PRRT)、生长抑素类似物、抗体药物偶联物(ADC)、促性腺激素释放激素(GnRH)类似物及其他基于肽的抗癌药物进行分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11326481/504aaf83d621/cancers-16-01032-g001.jpg

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