儿童胶质瘤MAPK改变的靶向治疗。

Brain disorders & therapy Pub Date : 2015-08-01 Epub Date: 2015-07-18 DOI:10.4172/2168-975X.S2-005
A Y Truong, T P Nicolaides
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引用次数: 4

摘要

尽管丝裂原活化蛋白激酶(MAPK)途径有助于促进正常细胞发育,但已知该途径有助于多种类型癌症的发生和生长。肿瘤发生可由该途径的许多关键蛋白的突变引起,包括但不限于RAS、三种RAF激酶中的任何一种或MEK1/2。此外,通过发现和理解致癌突变的生物学,科学家可以开发出新的靶向疗法。这篇综述描述了此类靶向治疗儿童胶质瘤的一般历史。我们首先描述了胶质瘤的生物学和MAPK途径中的致癌突变,然后总结了这些靶向治疗的显著临床前数据和临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Targeted Therapy for MAPK Alterations in Pediatric Gliomas.

Although the mitogen-activated protein kinase (MAPK) pathway helps promote normal cell development, the pathway is known to contribute to the initiation and growth of many types of cancers. Tumorigenesis can result from mutations in a number of the pathway's key proteins, including but not limited to RAS, any one of the three RAF kinases, or MEK1/2. Moreover, by discovering and understanding the biology of oncogenic mutations, scientists can develop novel targeted therapies. This review describes the general history of such targeted therapies in the context of pediatric gliomas. We first describe the biology of gliomas and oncogenic mutations in the MAPK pathway and then summarize notable pre-clinical data and clinical trials for these targeted therapies.

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