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分子特征与染色体不稳定性与 IDH 突变型和 IDH 野生型星形细胞瘤的拷贝数变异模式和患者预后相关。

Molecular Signatures of Chromosomal Instability Correlate With Copy Number Variation Patterns and Patient Outcome in IDH-Mutant and IDH-Wildtype Astrocytomas.

机构信息

From the Department of Pathology and Laboratory Medicine; University of Texas Health San Antonio, San Antonio, Texas, USA.

Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health San Antonio, San Antonio, Texas, USA.

出版信息

J Neuropathol Exp Neurol. 2021 Mar 22;80(4):354-365. doi: 10.1093/jnen/nlab008.

DOI:10.1093/jnen/nlab008
PMID:33755138
Abstract

Chromosomal instability due to mutations in genes guarding the stability of the genome is a well-known mechanism underlying tumorigenesis and malignant progression in numerous cancers. The effect of this process in gliomas is mostly unknown with relatively little research examining the effects of chromosomal instability on patient outcome and therapeutic efficacy, although studies have shown that overall/total copy number variation (CNV) is elevated in higher histologic grades and in cases with more rapid progression and shorter patient survival. Herein, we examine a 70-gene mRNA expression signature (CIN70), which has been previously shown to correlate tightly with chromosomal instability, in 2 independent cohorts of IDH-mutant astrocytomas (total n = 241), IDH-wildtype astrocytomas (n = 228), and oligodendrogliomas (n = 128). Our results show that CIN70 expression levels correlate with total CNV, as well as higher grade, progression-free survival, and overall survival in both IDH-mutant and IDH-wildtype astrocytomas. In oligodendrogliomas, these mRNA signatures correlate with total CNV but not consistently with clinical outcome. These data suggest that chromosomal instability is an underlying factor in aggressive behavior and progression of a subset of diffuse astrocytomas. In addition, chromosomal instability may in part explain the poor response of diffuse gliomas to treatment and may serve as a future therapeutic target.

摘要

由于基因突变为基因组稳定性保驾护航而导致的染色体不稳定是许多癌症发生和恶性进展的一个众所周知的机制。在神经胶质瘤中,这一过程的影响尚不完全清楚,相对较少的研究检查了染色体不稳定性对患者预后和治疗效果的影响,尽管研究表明,在较高的组织学分级、进展较快和患者生存时间较短的病例中,总拷贝数变异(CNV)升高。在此,我们研究了一个 70 个基因 mRNA 表达特征(CIN70),之前的研究表明它与染色体不稳定性密切相关,在 2 个独立的 IDH 突变型星形细胞瘤队列(总 n = 241)、IDH 野生型星形细胞瘤(n = 228)和少突胶质细胞瘤(n = 128)中进行了研究。我们的研究结果表明,CIN70 的表达水平与总 CNV 以及 IDH 突变型和 IDH 野生型星形细胞瘤的高级别、无进展生存期和总生存期相关。在少突胶质细胞瘤中,这些 mRNA 特征与总 CNV 相关,但与临床结局不一致。这些数据表明,染色体不稳定性是弥漫性星形细胞瘤亚组侵袭性行为和进展的一个潜在因素。此外,染色体不稳定性可能部分解释了弥漫性神经胶质瘤对治疗的反应较差,并可能成为未来的治疗靶点。

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