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


Journal

Journal of neuropathology and experimental neurology
ISSN: 1554-6578
Titre abrégé: J Neuropathol Exp Neurol
Pays: England
ID NLM: 2985192R

Informations de publication

Date de publication:
22 03 2021
Historique:
entrez: 23 3 2021
pubmed: 24 3 2021
medline: 31 12 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33755138
pii: 6180987
doi: 10.1093/jnen/nlab008
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

354-365

Informations de copyright

© 2021 American Association of Neuropathologists, Inc. All rights reserved.

Auteurs

Timothy E Richardson (TE)

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.

Adwait Amod Sathe (AA)

Eugene McDermott Center for Human Growth & Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Chao Xing (C)

Eugene McDermott Center for Human Growth & Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Kanish Mirchia (K)

Department of Pathology, State University of New York, Upstate Medical University, Syracuse, New York, USA.

Mariano S Viapiano (MS)

Department of Neuroscience and Physiology, State University of New York, Upstate Medical University, Syracuse, New York, USA.
Department of Neurosurgery, State University of New York, Upstate Medical University, Syracuse, New York, USA.

Matija Snuderl (M)

Department of Pathology, New York University Langone Health, New York City, New York, USA.

Kalil G Abdullah (KG)

Department of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Kimmo J Hatanpaa (KJ)

Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Jamie M Walker (JM)

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.

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