胶质母细胞瘤多形性细胞侵袭的基本机制综述

M. Waqas, S. Enam, M. Batool, H. Rai
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引用次数: 3

摘要

多形性胶质母细胞瘤(GBM)是最常见和最致命的原发性胶质肿瘤。GBM既可以“从头开始”发展,也可以从先前的星形细胞瘤进化而来,其特征是高增殖和浸润到周围组织。尽管采用了手术、放疗和化疗等多种治疗方式,但这种侵袭性行为是导致该癌症预后不良的最主要因素。了解和定位调节胶质瘤侵袭和进展的分子机制可能有助于确定GBM治疗的新靶点。本文将对Wnt、PI3K/Akt、sonic hedgehog-GLI1和microrna等信号通路进行综述,这些信号通路对GBM侵袭具有正调控和负调控作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Basic Mechanisms of Glioblastoma Multiforme Cell Invasion: A Review Article
Glioblastoma multiforme (GBM) is the most common and lethal primary glial neoplasm. GBM can develop both “de novo” or evolve from a previous astrocytoma, being characterized by high proliferation and infiltration into the surrounding tissue. This invasive behavior is the most contributing factor for the poor prognosis of this cancer, despite the multimodal treatment with surgery, radiotherapy and chemotherapy. Understanding and targeting the molecular mechanisms regulating glioma invasion and progression may help in identifying novel therapeutic targets for GBM treatment. This review will give an overview of some of the signaling pathways that have been shown to positively and negatively regulate GBM invasion, including the Wnt, PI3K/Akt, sonic hedgehog-GLI1 and microRNAs.
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