Literature DB >> 25965575

Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups.

Kristian W Pajtler1, Hendrik Witt2, Martin Sill3, David T W Jones4, Volker Hovestadt5, Fabian Kratochwil4, Khalida Wani6, Ruth Tatevossian7, Chandanamali Punchihewa7, Pascal Johann4, Jüri Reimand8, Hans-Jörg Warnatz9, Marina Ryzhova10, Steve Mack11, Vijay Ramaswamy12, David Capper13, Leonille Schweizer13, Laura Sieber4, Andrea Wittmann4, Zhiqin Huang5, Peter van Sluis14, Richard Volckmann14, Jan Koster14, Rogier Versteeg14, Daniel Fults15, Helen Toledano16, Smadar Avigad17, Lindsey M Hoffman18, Andrew M Donson18, Nicholas Foreman18, Ekkehard Hewer19, Karel Zitterbart20, Mark Gilbert21, Terri S Armstrong22, Nalin Gupta23, Jeffrey C Allen24, Matthias A Karajannis25, David Zagzag26, Martin Hasselblatt27, Andreas E Kulozik28, Olaf Witt29, V Peter Collins30, Katja von Hoff31, Stefan Rutkowski31, Torsten Pietsch32, Gary Bader8, Marie-Laure Yaspo9, Andreas von Deimling13, Peter Lichter33, Michael D Taylor11, Richard Gilbertson34, David W Ellison7, Kenneth Aldape35, Andrey Korshunov13, Marcel Kool36, Stefan M Pfister37.   

Abstract

Ependymal tumors across age groups are currently classified and graded solely by histopathology. It is, however, commonly accepted that this classification scheme has limited clinical utility based on its lack of reproducibility in predicting patients' outcome. We aimed at establishing a uniform molecular classification using DNA methylation profiling. Nine molecular subgroups were identified in a large cohort of 500 tumors, 3 in each anatomical compartment of the CNS, spine, posterior fossa, supratentorial. Two supratentorial subgroups are characterized by prototypic fusion genes involving RELA and YAP1, respectively. Regarding clinical associations, the molecular classification proposed herein outperforms the current histopathological classification and thus might serve as a basis for the next World Health Organization classification of CNS tumors.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25965575      PMCID: PMC4712639          DOI: 10.1016/j.ccell.2015.04.002

Source DB:  PubMed          Journal:  Cancer Cell        ISSN: 1535-6108            Impact factor:   31.743


  52 in total

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Journal:  Cancer Cell       Date:  2011-08-16       Impact factor: 31.743

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Journal:  Cancer Cell       Date:  2012-10-16       Impact factor: 31.743

10.  Genetic abnormalities detected in ependymomas by comparative genomic hybridisation.

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  326 in total

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2.  Discovery of New Fusion Transcripts in a Cohort of Pediatric Solid Cancers at Relapse and Relevance for Personalized Medicine.

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Review 4.  Recent advances in intradural spinal tumors.

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7.  Molecular heterogeneity and CXorf67 alterations in posterior fossa group A (PFA) ependymomas.

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Review 9.  Improving Diagnostic and Therapeutic Outcomes in Pediatric Brain Tumors.

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