ConsistentSMARCB1homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material-Reference-Cited by-同舟云学术

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ConsistentSMARCB1homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material

Published:2014-03-03 Issue:6 Volume:53 Page:475-486
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Le Loarer Francois¹²,Zhang Lei¹,Fletcher Christopher D.³,Ribeiro Agnes²,Singer Samuel⁴,Italiano Antoine⁵,Neuville Agnes²,Houlier Aurélie⁶,Chibon Frederic²⁷,Coindre Jean-Michel²⁷,Antonescu Cristina R.¹

Affiliation:

1. Pathology Department; Memorial Sloan-Kettering Cancer Center; New York NY

2. Pathology Department; Institut Bergonié Cancer Center; Bordeaux France

3. Department of Pathology; Brigham & Women's Hospital; Boston MA

4. Surgery Department; Memorial Sloan-Kettering Cancer Center; New York NY

5. Oncology Department; Institut Bergonié Cancer Center; Bordeaux France

6. Pathology Department; Centre Leon Berard; Lyon France

7. Sarcoma Biology Research Center, INSERM U916 and Université Bordeaux 2; Bordeaux France

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gcc.22159/fullpdf

Reference38 articles.

1. Aurora kinase A outperforms Ki67 as a prognostic marker in ER-positive breast cancer;Ali;Br J Cancer,2012

2. EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene;Antonescu;Genes Chromosomes Cancer,2010

3. Novel ZC3H7B-BCOR, MEAF6-PHF1, and EPC1-PHF1 fusions in ossifying fibromyxoid tumors-molecular characterization shows genetic overlap with endometrial stromal sarcoma;Antonescu;Genes Chromosomes Cancer,2014

4. Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation;Bacci;Neurogenetics,2010

5. hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities;Bourdeaut;J Pathol,2007

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