Loyola University Chicago, Stritch School of Medicine, Division of Hematology/Oncology, Department of Medicine, 2160 S 1st Avenue Maywood, IL 60153, USA.
Expert Opin Investig Drugs. 2009 Sep;18(9):1375-83. doi: 10.1517/13543780903158934.
Heat shock proteins are vital to cell survival under conditions of stress. They bind client proteins to assist in protein stabilization, translocation of polypeptides across cell membranes and recovery of proteins from aggregates. Heat shock protein inhibitors are a diverse group of novel agents that have been demonstrated to have pro-apoptotic effects on malignant cells through inhibition of ATP binding on the ATP/ADP-binding pocket of the heat shock protein. Initial development of heat shock protein 90 inhibitors, geldanamycin and 17-AAG, were limited by hepatotoxicity and the need for solvent carrying agents. In contrast, retaspimycin, or IPI-504, a derivative of geldanamycin and 17-AAG, is highly soluble in water and generally well tolerated. In Phase I/II trials, retaspimycin has shown activity in NSCLC and gastrointestinal stromal tumor. The most promising activity was observed in gastrointestinal stromal tumors. Phase I/II trials are currently underway to evaluate the dosing schedules and activity of IPI-504 in breast cancer. Given the in vitro activity in diffuse large B-cell lymphoma, mantle cell lymphoma, melanoma, leukemia and pancreatic cancer, current and future trials are of clinical interest. This article reviews IPI-504 and its utility in a wide variety of cancer phenotypes.
热休克蛋白在应激条件下对细胞存活至关重要。它们与客户蛋白结合,以协助蛋白质稳定、多肽跨细胞膜转运和蛋白质从聚集体中恢复。热休克蛋白抑制剂是一组多样化的新型药物,通过抑制热休克蛋白的 ATP/ADP 结合口袋上的 ATP 结合,对恶性细胞具有促凋亡作用。热休克蛋白 90 抑制剂格尔德霉素和 17-AAG 的最初开发受到肝毒性和溶剂携带剂的需要的限制。相比之下,retaspimycin(或 IPI-504)是格尔德霉素和 17-AAG 的衍生物,在水中高度溶解,通常耐受性良好。在 I/II 期临床试验中,retaspimycin 在非小细胞肺癌和胃肠道间质瘤中显示出活性。最有前途的活性在胃肠道间质瘤中观察到。目前正在进行 I/II 期临床试验,以评估 IPI-504 在乳腺癌中的剂量方案和活性。鉴于在弥漫性大 B 细胞淋巴瘤、套细胞淋巴瘤、黑色素瘤、白血病和胰腺癌中的体外活性,目前和未来的试验具有临床意义。本文综述了 IPI-504 及其在多种癌症表型中的应用。