Delineation of two clinically and molecularly distinct subgroups of posterior fossa ependymoma.

نویسندگان

  • Hendrik Witt
  • Stephen C Mack
  • Marina Ryzhova
  • Sebastian Bender
  • Martin Sill
  • Ruth Isserlin
  • Axel Benner
  • Thomas Hielscher
  • Till Milde
  • Marc Remke
  • David T W Jones
  • Paul A Northcott
  • Livia Garzia
  • Kelsey C Bertrand
  • Andrea Wittmann
  • Yuan Yao
  • Stephen S Roberts
  • Luca Massimi
  • Tim Van Meter
  • William A Weiss
  • Nalin Gupta
  • Wiesia Grajkowska
  • Boleslaw Lach
  • Yoon-Jae Cho
  • Andreas von Deimling
  • Andreas E Kulozik
  • Olaf Witt
  • Gary D Bader
  • Cynthia E Hawkins
  • Uri Tabori
  • Abhijit Guha
  • James T Rutka
  • Peter Lichter
  • Andrey Korshunov
  • Michael D Taylor
  • Stefan M Pfister
چکیده

Despite the histological similarity of ependymomas from throughout the neuroaxis, the disease likely comprises multiple independent entities, each with a distinct molecular pathogenesis. Transcriptional profiling of two large independent cohorts of ependymoma reveals the existence of two demographically, transcriptionally, genetically, and clinically distinct groups of posterior fossa (PF) ependymomas. Group A patients are younger, have laterally located tumors with a balanced genome, and are much more likely to exhibit recurrence, metastasis at recurrence, and death compared with Group B patients. Identification and optimization of immunohistochemical (IHC) markers for PF ependymoma subgroups allowed validation of our findings on a third independent cohort, using a human ependymoma tissue microarray, and provides a tool for prospective prognostication and stratification of PF ependymoma patients.

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عنوان ژورنال:
  • Cancer cell

دوره 20 2  شماره 

صفحات  -

تاریخ انتشار 2011