Vismodegib, a small-molecule inhibitor of the hedgehog pathway for the treatment of advanced cancers.

Enrico De Smaele, Elisabetta Ferretti, Alberto Gulino
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Abstract

Vismodegib (GDC-0449) is a small, orally administrable molecule, belonging to the 2-arylpyridine class, which was discovered by Genentech Inc under a collaboration with Curis Inc. Vismodegib inhibits the Hedgehog (Hh) pathway, which is involved in tumorigenesis, thus providing a strong rationale for its use in the treatment of a variety of cancers. Vismodegib suppresses Hh signaling by binding to and interfering with smoothened, a membrane protein that provides positive signals to the Hh signaling pathway. Preclinical studies demonstrated the antitumor activity of vismodegib in mouse models of medulloblastoma (MB) and in xenograft models of colorectal and pancreatic cancer. Phase I clinical trials in patients with advanced basal cell carcinoma (BCC) and MB highlighted an objective response to vismodegib. Reported side effects were minor, with only one grade 4 adverse event. Vismodegib is currently undergoing phase II clinical trials for the treatment of advanced BCC, metastatic colorectal cancer, ovarian cancer, MB and other solid tumors. Because of its low toxicity and specificity for the Hh pathway, this drug has potential advantages compared with conventional chemotherapy, and may also be used in combination treatments. Clinical trials with other Hh inhibitors are also ongoing and their therapeutic potential will need to be compared with vismodegib.

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Vismodegib,一种用于治疗晚期癌症的小分子hedgehog通路抑制剂。
Vismodegib (GDC-0449)是一种口服小分子,属于2-芳基吡啶类,由Genentech公司与Curis公司合作发现。Vismodegib抑制参与肿瘤发生的Hedgehog (Hh)通路,因此为其用于治疗多种癌症提供了强有力的依据。Vismodegib通过结合和干扰smoothened来抑制Hh信号通路,smoothened是一种向Hh信号通路提供积极信号的膜蛋白。临床前研究表明,vismodegib在成神经管细胞瘤(MB)小鼠模型和结直肠癌和胰腺癌异种移植模型中具有抗肿瘤活性。晚期基底细胞癌(BCC)和MB患者的I期临床试验强调了对vismodegib的客观反应。报告的副作用很小,只有一个4级不良事件。Vismodegib目前正在进行II期临床试验,用于治疗晚期BCC、转移性结直肠癌、卵巢癌、MB和其他实体肿瘤。由于其低毒性和Hh通路特异性,与常规化疗相比,该药物具有潜在的优势,也可用于联合治疗。其他Hh抑制剂的临床试验也在进行中,其治疗潜力将需要与vismodegib进行比较。
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