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RGD 整联蛋白亚型特异性配体在癌症中的生物学相关性。

Biological Relevance of RGD-Integrin Subtype-Specific Ligands in Cancer.

机构信息

Laboratoire de Bioimagerie et Pathologies (LBP), UMR CNRS 7021, Institut Thématique Interdisciplinaire InnoVec, Université de Strasbourg, Faculté de Pharmacie, 74 route du, Rhin, CS 60024, 67401, Illkirch Cedex, France.

Cancer and Diabetic Research Group, Department of Biochemistry and Molecular Biology, Faculty of Science, Federal University Ndufu-Alike Ikwo, P.M.B, 1010, Abakaliki, Ebonyi State, Nigeria.

出版信息

Chembiochem. 2021 Apr 6;22(7):1151-1160. doi: 10.1002/cbic.202000626. Epub 2020 Nov 27.

DOI:10.1002/cbic.202000626
PMID:33140906
Abstract

Integrins are heterodimeric transmembrane proteins able to connect cells with the micro-environment. They represent a family of receptors involved in almost all the hallmarks of cancer. Integrins recognizing the Arg-Gly-Asp (RGD) peptide in their natural extracellular matrix ligands have been particularly investigated as tumoral therapeutic targets. In the last 30 years, intense research has been dedicated to designing specific RGD-like ligands able to discriminate selectively the different RGD-recognizing integrins. Chemists' efforts have led to the proposition of modified peptide or peptidomimetic libraries to be used for tumor targeting and/or tumor imaging. Here we review, from the biological point of view, the rationale underlying the need to clearly delineate each RGD-integrin subtype by selective tools. We describe the complex roles of RGD-integrins (mainly the most studied αvβ3 and α5β1 integrins) in tumors, the steps towards selective ligands and the current usefulness of such ligands. Although the impact of integrins in cancer is well acknowledged, the biological characteristics of each integrin subtype in a specific tumor are far from being completely resolved. Selective ligands might help us to reconsider integrins as therapeutic targets in specific clinical settings.

摘要

整合素是一种能够将细胞与微环境连接起来的异二聚体跨膜蛋白。它们是一类受体家族,几乎参与了癌症的所有特征。整合素识别其天然细胞外基质配体中的精氨酸-甘氨酸-天冬氨酸(RGD)肽,已被特别研究作为肿瘤治疗靶点。在过去的 30 年中,人们致力于设计能够选择性区分不同 RGD 识别整合素的特异性 RGD 样配体。化学家们的努力导致了对修饰肽或拟肽文库的提出,这些文库可用于肿瘤靶向和/或肿瘤成像。在这里,我们从生物学角度回顾了需要通过选择性工具清楚地区分每个 RGD-整合素亚型的基本原理。我们描述了 RGD-整合素(主要是研究最多的 αvβ3 和 α5β1 整合素)在肿瘤中的复杂作用、选择性配体的步骤以及此类配体的当前用途。尽管整合素在癌症中的作用已得到充分认可,但每种特定肿瘤中整合素亚型的生物学特征远未完全解决。选择性配体可能有助于我们在特定临床环境中将整合素重新视为治疗靶点。

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