[脑膜瘤基因/分子异常分析和预后预测的现状]。

Q4 Medicine Neurological Surgery Pub Date : 2024-07-01 DOI:10.11477/mf.1436204971
Atsushi Okano
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引用次数: 0

摘要

随着分子生物学方法的发展,脑膜瘤的生物分子研究也得到了发展。2013年,Clark等报道,除NF2外,包括TRAF7、KLF4、AKT1和SMO在内的驱动基因突变与脑膜瘤的发生相关。2017年,Sahm等人提出了一种基于全局甲基化状态的脑膜瘤分类方法,该方法在预测预后方面比传统的WHO分级更准确。2022年,在此分类基础上,不同研究小组报告了一种综合分类,全面包括了一些生物分子异常,如DNA突变、拷贝数改变和RNA序列。这一领域有望阐明脑膜瘤的发展机制,进一步的研究有望在未来开发出有效的分子靶向治疗药物和放射敏感性生物标志物。本文总结了这些生物分子研究的现状和前景。
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[Current Status of Genetic/Molecular Abnormality Analysis and Prognosis Prediction of Meningioma].

Biological molecular studies of meningiomas have also developed with the development of molecular biological methods. In 2013, Clark et al. reported that driver genetic mutations other than NF2, including TRAF7, KLF4, AKT1, and SMO, were associated with meningioma development. In 2017, Sahm et al. proposed a classification of meningiomas based on global methylation status, which was more accurate in predicting prognosis than conventional WHO grading. In 2022, based on this classification, various groups reported an integrated classification that comprehensively included some biological molecular abnormalities, such as DNA mutations, copy number alterations, and RNA sequences. This field is expected to elucidate the mechanism of meningioma development and further research is expected to lead to the development of effective molecularly targeted therapeutics and biomarkers of radiosensitivity in the future. In this article, we summarize the current status and prospects of these biological molecular studies.

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来源期刊
Neurological Surgery
Neurological Surgery Medicine-Medicine (all)
自引率
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发文量
99
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