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纳米策略用于胃泌素释放肽受体的治疗和诊断靶向。

Nanostrategies for Therapeutic and Diagnostic Targeting of Gastrin-Releasing Peptide Receptor.

机构信息

Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Wroblewskiego 15, 93-590 Lodz, Poland.

Department of Cell Cultures and Genomic Analysis, Medical University of Lodz, Zeligowskiego 7/9, 90-752 Lodz, Poland.

出版信息

Int J Mol Sci. 2023 Feb 9;24(4):3455. doi: 10.3390/ijms24043455.

Abstract

Advances in nanomedicine bring the attention of researchers to the molecular targets that can play a major role in the development of novel therapeutic and diagnostic modalities for cancer management. The choice of a proper molecular target can decide the efficacy of the treatment and endorse the personalized medicine approach. Gastrin-releasing peptide receptor (GRPR) is a G-protein-coupled membrane receptor, well known to be overexpressed in numerous malignancies including pancreatic, prostate, breast, lung, colon, cervical, and gastrointestinal cancers. Therefore, many research groups express a deep interest in targeting GRPR with their nanoformulations. A broad spectrum of the GRPR ligands has been described in the literature, which allows tuning of the properties of the final formulation, particularly in the field of the ligand affinity to the receptor and internalization possibilities. Hereby, the recent advances in the field of applications of various nanoplatforms that are able to reach the GRPR-expressing cells are reviewed.

摘要

纳米医学的进展引起了研究人员对分子靶点的关注,这些靶点在开发新型治疗和诊断方法以管理癌症方面可以发挥重要作用。选择适当的分子靶点可以决定治疗的效果,并支持个性化医疗方法。胃泌素释放肽受体(GRPR)是一种 G 蛋白偶联膜受体,已知在许多恶性肿瘤中过度表达,包括胰腺、前列腺、乳腺、肺、结肠、宫颈和胃肠道癌症。因此,许多研究小组对用他们的纳米制剂靶向 GRPR 表达表现出浓厚的兴趣。文献中描述了广泛的 GRPR 配体,这允许调整最终制剂的特性,特别是在配体与受体的亲和力和内化可能性方面。在此,综述了目前能够到达 GRPR 表达细胞的各种纳米平台应用领域的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c0/9958678/b135db3df0fd/ijms-24-03455-g001.jpg

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