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支架蛋白在胶质母细胞瘤异质性中的作用。

Role of scaffold proteins in the heterogeneity of glioblastoma.

机构信息

Department of Medicine, Division of Hematology and Oncology, College of Medicine and Life Sciences, Health Sciences Campus, The University of Toledo, 352A Health Science Building, 3000 Transverse Drive, Toledo, OH, 43614, USA.

Division of Neuropathology, Department of Pathology, Rhode Island Hospital and the Warren Alpert Medical School of Brown University, Providence, RI, 02903, USA.

出版信息

Cell Commun Signal. 2024 Oct 7;22(1):477. doi: 10.1186/s12964-024-01809-1.

Abstract

Glioblastoma (GB) is a highly heterogeneous type of incurable brain cancer with a low survival rate. Intensive ongoing research has identified several potential targets; however, GB is marred by the activation of multiple pathways, and thus common targets are highly sought. The signal regulatory scaffold IQGAP1 is an oncoprotein implicated in GB. IQGAP1 nucleates a myriad of pathways in a contextual manner and modulates many of the targets altered in GB like MAPK, NF-κB, and mTOR/PI3K/Akt1, thus positioning it as a plausible common therapeutic target. Here, we review the targets that are subjects of GB treatment clinical trials and the commonly used animal models that facilitate target identification. We propose a model in which the dysfunction of various IQGAP1 pathways can explain to a larger extent some of the GB heterogeneity and offer a platform for personalized medicine.

摘要

胶质母细胞瘤(GB)是一种高度异质性的不可治愈的脑癌,其存活率较低。正在进行的深入研究已经确定了几个潜在的靶点;然而,GB 受到多种途径的激活的影响,因此高度需要常见的靶点。信号调节支架 IQGAP1 是一种在胶质母细胞瘤中起作用的癌蛋白。IQGAP1 以上下文的方式引发无数途径,并调节许多在 GB 中改变的靶点,如 MAPK、NF-κB 和 mTOR/PI3K/Akt1,因此将其定位为一个合理的共同治疗靶点。在这里,我们回顾了作为 GB 治疗临床试验对象的靶点和促进靶点识别的常用动物模型。我们提出了一个模型,其中各种 IQGAP1 途径的功能障碍可以在更大程度上解释一些 GB 的异质性,并为个性化医疗提供一个平台。

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