SHH inhibitors for the treatment of medulloblastoma

髓母细胞瘤 PTCH1型 音猬因子 刺猬信号通路 修补 癌症研究 生物 平滑 刺猬 维莫德吉 信号转导 遗传学
作者
Ayman Samkari,Jason C. White,Roger J. Packer
出处
期刊:Expert Review of Neurotherapeutics [Taylor & Francis]
卷期号:15 (7): 763-770 被引量:39
标识
DOI:10.1586/14737175.2015.1052796
摘要

Medulloblastoma is the most common malignant brain tumor of childhood. It is currently stratified into four molecular variants through the advances in transcriptional profiling. They include: wingless, sonic hedgehog (SHH), Group III, and Group IV. The SHH group is characterized by constitutive activation of the SHH signaling pathway, and genetically characterized by mutations in patched homolog 1 (PTCH1) or other downstream pathway mutations. SHH inhibitors have become of great clinical interest in treating SHH-driven medulloblastoma. Many inhibitors are currently in different stages of development, some already approved for other SHH-driven cancers, such as basal cell carcinoma. In vitro and in vivo medulloblastoma studies have shown efficacy and these findings have been translated into Phase I and II clinical trials. In this review, we present an overview of SHH medulloblastoma, as well as a discussion of currently available SHH inhibitors, and the challenges associated with their use.

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