Al Musaimi Othman
School of Pharmacy, Faculty of Medical Sciences, Newcastle upon Tyne NE1 7RU, UK.
Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK.
Cancers (Basel). 2024 Mar 2;16(5):1032. doi: 10.3390/cancers16051032.
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.
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。