Tolomelli Alessandra, Galletti Paola, Baiula Monica, Giacomini Daria
Department of Chemistry "G. Ciamician", University of Bologna, Via Selmi 2, 40126 Bologna, Italy.
Department of Pharmacy and Biotechnology, University of Bologna, Via Irnerio 48, 40126 Bologna, Italy.
Cancers (Basel). 2017 Jul 5;9(7):78. doi: 10.3390/cancers9070078.
The ability of integrins to activate and integrate intracellular communication illustrates the potential of these receptors to serve as functional distribution hubs in a bi-directional signal transfer outside-in and inside-out of the cells. Tight regulation of the integrin signaling is paramount for normal physiological functions such as migration, proliferation, and differentiation, and misregulated integrin activity could be associated with several pathological conditions. Because of the important roles of integrins and their ligands in biological development, immune responses, leukocyte traffic, haemostasis, and cancer, their potential as therapeutic tools is now widely recognized. Nowadays extensive efforts have been made to discover and develop small molecule ligands as integrin antagonists, whereas less attention has been payed to agonists. In recent years, it has been recognized that integrin agonists could open up novel opportunities for therapeutics, which gain benefits to increase rather than decrease integrin-dependent adhesion and transductional events. For instance, a significant factor in chemo-resistance in melanoma is a loss of integrin-mediated adhesion; in this case, stimulation of integrin signaling by agonists significantly improved the response to chemotherapy. In this review, we overview results about small molecules which revealed an activating action on some integrins, especially those involved in cancer, and examine from a medicinal chemistry point of view, their structure and behavior.
整合素激活和整合细胞内通讯的能力表明,这些受体有潜力在细胞外向内和细胞内向外的双向信号传递中充当功能分布枢纽。整合素信号的严格调控对于迁移、增殖和分化等正常生理功能至关重要,而整合素活性失调可能与多种病理状况相关。由于整合素及其配体在生物发育、免疫反应、白细胞运输、止血和癌症中发挥着重要作用,它们作为治疗工具的潜力目前已得到广泛认可。如今,人们已付出大量努力来发现和开发作为整合素拮抗剂的小分子配体,而对激动剂的关注较少。近年来,人们认识到整合素激动剂可为治疗开辟新机遇,其益处在于增加而非减少整合素依赖性黏附及转导事件。例如,黑色素瘤化疗耐药的一个重要因素是整合素介导的黏附丧失;在这种情况下,激动剂刺激整合素信号可显著改善化疗反应。在本综述中,我们概述了有关对某些整合素(尤其是那些与癌症相关的整合素)具有激活作用的小分子的研究结果,并从药物化学角度研究它们的结构和行为。