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肿瘤穿透肽内化 RGD 用于癌症治疗和诊断的最新进展。

Recent advances in the tumor-penetrating peptide internalizing RGD for cancer treatment and diagnosis.

机构信息

Faculty of Life science and Technology, Kunming University of Science and Technology, Kunming, People's Republic of China.

Medical School, Kunming University of Science and Technology, Kunming, People's Republic of China.

出版信息

Drug Dev Res. 2023 Jun;84(4):654-670. doi: 10.1002/ddr.22056. Epub 2023 Apr 5.

Abstract

Cancer has become a prominent disease that seriously endangers human health. The complexity of the biological characteristics of the tumor makes it challenging for traditional therapeutic drugs to penetrate tumor tissues and exert their antitumor effects. Internalizing RGD peptide (iRGD) is a novel tumor-homing peptide that binds to αvβ3 and αvβ5 integrins on the surface of tumor vessels through the C-end rule (CendR) motif. The CendR motif binds to the neuropilin-1 (NRP-1) receptor on tumor cells, initiating NRP-1-mediated transcytosis to facilitate drug entry into the tumor tissue. Multiple studies demonstrated that iRGD improved the penetration and targeting of antitumor drugs, thereby enhancing their antitumor efficacy. In this review, we initially described the origins of iRGD and its penetration mechanism. Furthermore, we presented updates on the application of iRGD in cancer chemotherapy, photodynamic therapy, gene therapy, immunotherapy, treatment with antibodies or protein-based biologics, and tumor imaging.

摘要

癌症已成为严重危害人类健康的突出疾病。肿瘤的生物学特性十分复杂,这使得传统治疗药物难以穿透肿瘤组织并发挥其抗肿瘤作用。内化 RGD 肽(iRGD)是一种新型的肿瘤归巢肽,通过 C 端规则(CendR)基序与肿瘤血管表面的αvβ3 和 αvβ5 整合素结合。CendR 基序与肿瘤细胞上的神经纤毛蛋白-1(NRP-1)受体结合,启动 NRP-1 介导的转胞吞作用,促进药物进入肿瘤组织。多项研究表明,iRGD 提高了抗肿瘤药物的穿透性和靶向性,从而增强了其抗肿瘤疗效。在这篇综述中,我们首先描述了 iRGD 的起源及其穿透机制。此外,我们还介绍了 iRGD 在癌症化疗、光动力疗法、基因治疗、免疫治疗、抗体或基于蛋白质的生物制剂治疗以及肿瘤成像中的应用进展。

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