TERT启动子突变在成人型弥漫性胶质瘤中的预后意义。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Brain Tumor Pathology Pub Date : 2022-07-01 Epub Date: 2022-01-31 DOI:10.1007/s10014-021-00424-z
Hideyuki Arita, Koichi Ichimura
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引用次数: 7

摘要

TERT启动子突变是成人型弥漫性胶质瘤中最常见的遗传改变之一,与胶质瘤亚型的其他遗传改变相比,TERT启动子突变显示出特定的模式。该突变与其他遗传改变(包括IDH1/2突变或组织学类型)相关,对患者预后有不同的影响。本文的目的是回顾目前关于TERT启动子突变在成人型弥漫性胶质瘤诊断和预后中的价值的知识。我们还旨在讨论TERT启动子突变和其他分子改变对预后影响之间的相互作用。尽管TERT启动子对预后的影响有些复杂和神秘,但在以IDH1/2和1p/19q状态定义的胶质瘤常规分类中,TERT启动子的突变状态为预测患者的预后提供了非常有用的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic significance of TERT promoter mutations in adult-type diffuse gliomas.

TERT promoter mutations are one of the most common genetic alterations in adult-type diffuse gliomas and show specific patterns compared with other genetic alterations according to glioma subtypes. This mutation has variable impacts on patient outcomes in association with other genetic alterations, including IDH1/2 mutations or histological types. The purpose of this paper is to review the current knowledge on the values of TERT promoter mutations in the diagnosis and prognostication of adult-type diffuse gliomas. We also aimed to discuss the interaction between the prognostic impacts of TERT promoter mutations and other molecular alterations. Although its impact on prognosis is somewhat complicated and enigmatic, the mutational status of the TERT promoter provides highly useful information for predicting patients' outcomes in the conventional classification of gliomas defined by IDH1/2 and 1p/19q status.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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