Literature DB >> 20159821

Genomic changes in chromosomes 10, 16, and X in malignant peripheral nerve sheath tumors identify a high-risk patient group.

Helge R Brekke1, Franclim R Ribeiro, Matthias Kolberg, Trude H Agesen, Guro E Lind, Mette Eknaes, Kirsten S Hall, Bodil Bjerkehagen, Eva van den Berg, Manuel R Teixeira, Nils Mandahl, Sigbjørn Smeland, Fredrik Mertens, Rolf I Skotheim, Ragnhild A Lothe.   

Abstract

PURPOSE: The purpose of this study was to identify genetic aberrations contributing to clinical aggressiveness of malignant peripheral nerve sheath tumors (MPNSTs). PATIENTS AND METHODS: Samples from 48 MPNSTs and 10 neurofibromas were collected from 51 patients with (n = 31) or without (n = 20) neurofibromatosis type 1 (NF1). Genome-wide DNA copy number changes were assessed by chromosomal and array-based comparative genomic hybridization (CGH) and examined for prognostic significance. For a subset of 20 samples, RNA microarray data were integrated with the genome data to identify potential target genes.
RESULTS: Forty-four (92%) MPNSTs displayed DNA copy number changes (median, 18 changes per tumor; range, 2 to 35 changes). Known frequent chromosomal gains at chromosome arms 8q (69%), 17q (67%), and 7p (52%) and losses from 9p (50%), 11q (48%), and 17p (44%) were confirmed. Additionally, gains at 16p or losses from 10q or Xq identified a high-risk group with only 11% 10-year disease-specific survival (P = .00005). Multivariate analyses including NF1 status, tumor location, size, grade, sex, complete remission, and initial metastatic status showed that the genomic high-risk group was the most significant predictor of poor survival. Several genes whose expression was affected by the DNA copy number aberrations were identified.
CONCLUSION: The presence of specific genetic aberrations was strongly associated with poor survival independent of known clinical risk factors. Conversely, within the total patient cohort with 34% 10-year disease-specific survival, a low-risk group was identified: without changes at chromosomes 10q, 16p, or Xq in their MPNSTs, the patients had 74% 10-year survival.

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Year:  2010        PMID: 20159821     DOI: 10.1200/JCO.2009.24.8989

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  18 in total

1.  Telomere maintenance mechanisms in malignant peripheral nerve sheath tumors: expression and prognostic relevance.

Authors:  Lorenza Venturini; Maria Grazia Daidone; Rosita Motta; Graziella Cimino-Reale; Stacey F Hoare; Alessandro Gronchi; Marco Folini; William Nicol Keith; Nadia Zaffaroni
Journal:  Neuro Oncol       Date:  2012-04-19       Impact factor: 12.300

2.  Current treatment options for malignant peripheral nerve sheath tumors.

Authors:  Diana Bradford; AeRang Kim
Journal:  Curr Treat Options Oncol       Date:  2015-03

3.  Clinical Outcome After Pencil Beam Scanning Proton Therapy of Patients With Non-Metastatic Malignant and Benign Peripheral Nerve Sheath Tumors.

Authors:  Nicolas Bachmann; Dominic Leiser; Alessia Pica; Barbara Bachtiary; Damien C Weber
Journal:  Front Oncol       Date:  2022-06-27       Impact factor: 5.738

4.  Canonical Wnt/β-catenin signaling drives human schwann cell transformation, progression, and tumor maintenance.

Authors:  Adrienne L Watson; Eric P Rahrmann; Branden S Moriarity; Kwangmin Choi; Caitlin B Conboy; Andrew D Greeley; Amanda L Halfond; Leah K Anderson; Brian R Wahl; Vincent W Keng; Anthony E Rizzardi; Colleen L Forster; Margaret H Collins; Aaron L Sarver; Margaret R Wallace; Stephen C Schmechel; Nancy Ratner; David A Largaespada
Journal:  Cancer Discov       Date:  2013-03-27       Impact factor: 39.397

Review 5.  Malignant peripheral nerve sheath tumors.

Authors:  Mohamad Farid; Elizabeth G Demicco; Roberto Garcia; Linda Ahn; Pamela R Merola; Angela Cioffi; Robert G Maki
Journal:  Oncologist       Date:  2014-01-27

Review 6.  Survival meta-analyses for >1800 malignant peripheral nerve sheath tumor patients with and without neurofibromatosis type 1.

Authors:  Matthias Kolberg; Maren Høland; Trude H Agesen; Helge R Brekke; Knut Liestøl; Kirsten S Hall; Fredrik Mertens; Piero Picci; Sigbjørn Smeland; Ragnhild A Lothe
Journal:  Neuro Oncol       Date:  2012-11-15       Impact factor: 12.300

7.  Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discovery.

Authors:  GuangJun Zhang; Sebastian Hoersch; Adam Amsterdam; Charles A Whittaker; Eline Beert; Julian M Catchen; Sarah Farrington; John H Postlethwait; Eric Legius; Nancy Hopkins; Jacqueline A Lees
Journal:  PLoS Genet       Date:  2013-08-29       Impact factor: 5.917

8.  Gender dimorphism and age of onset in malignant peripheral nerve sheath tumor preclinical models and human patients.

Authors:  Elizabeth Shurell; Linh M Tran; Jonathan Nakashima; Kathleen B Smith; Brenna M Tam; Yunfeng Li; Sarah M Dry; Noah Federman; William D Tap; Hong Wu; Fritz C Eilber
Journal:  BMC Cancer       Date:  2014-11-15       Impact factor: 4.430

9.  Molecular heterogeneity in malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1.

Authors:  Laura Thomas; Victor-Felix Mautner; David N Cooper; Meena Upadhyaya
Journal:  Hum Genomics       Date:  2012-09-04       Impact factor: 4.639

10.  Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.

Authors:  Stine A Danielsen; Guro E Lind; Matthias Kolberg; Maren Høland; Bodil Bjerkehagen; Kirsten Sundby Hall; Eva van den Berg; Fredrik Mertens; Sigbjørn Smeland; Piero Picci; Ragnhild A Lothe
Journal:  Neuro Oncol       Date:  2014-07-19       Impact factor: 12.300

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