Brain Invasion and Trends in Molecular Research on Meningioma.

Kyeong-O Go, Young Zoon Kim
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引用次数: 2

Abstract

Meningiomas are the most common primary brain tumors in adults. The treatment of non-benign meningiomas remains a challenging task, and after the publication of the 2021 World Health Organization classification, the importance of molecular biological classification is emerging. In this article, we introduce the mechanisms of brain invasion in atypical meningioma and review the genetic factors involved along with epigenetic regulation. First, it is important to understand the three major steps for brain invasion of meningeal cells: 1) degradation of extracellular matrix by proteases, 2) promotion of tumor cell migration to resident cells by adhesion molecules, and 3) neovascularization and supporting cells by growth factors. Second, the genomic landscape of meningiomas should be analyzed by major categories, such as germline mutations in NF2 and somatic mutations in non-NF2 genes (TRAF7, KLF4, AKT1, SMO, and POLR2A). Finally, epigenetic alterations in meningiomas are being studied, with a focus on DNA methylation, histone modification, and RNA interference. Increasing knowledge of the molecular landscape of meningiomas has allowed the identification of prognostic and predictive markers that can guide therapeutic decision-making processes and the timing of follow-up.

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脑膜瘤的脑侵及分子研究进展。
脑膜瘤是成人最常见的原发性脑肿瘤。非良性脑膜瘤的治疗仍然是一项具有挑战性的任务,在世界卫生组织2021年分类公布后,分子生物学分类的重要性正在显现。本文就非典型脑膜瘤侵袭脑的机制作一介绍,并对其涉及的遗传因素及表观遗传调控进行综述。首先,了解脑膜细胞侵袭大脑的三个主要步骤是很重要的:1)蛋白酶降解细胞外基质,2)粘附分子促进肿瘤细胞向驻留细胞迁移,3)生长因子形成新生血管和支持细胞。其次,脑膜瘤的基因组图谱应按主要类别进行分析,如NF2的种系突变和非NF2基因(TRAF7、KLF4、AKT1、SMO和POLR2A)的体细胞突变。最后,脑膜瘤的表观遗传改变正在被研究,重点是DNA甲基化、组蛋白修饰和RNA干扰。随着对脑膜瘤分子结构知识的不断增加,人们可以确定预后和预测标记物,从而指导治疗决策过程和随访时间。
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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