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1 November 2014
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Using next-generation sequencing, Crompton, Stewart, and colleagues found that Ewing sarcoma tumors were relatively genetically stable, but exhibited recurrent loss of stromal antigen 2 (STAG2) expression, which was associated with metastatic progression. In addition, relapsed tumors displayed an increased mutation rate compared with tumors at diagnosis. Using whole-genome sequencing, Tirode, Surdez, and colleagues also detected few somatic alterations in Ewing sarcoma and identified STAG2 as the most frequently mutated gene. STAG2 mutations were mutually exclusive with CDKN2A deletion, but often coexisted with TP53 mutations, were associated with poor outcome, and expanded at tumor relapse. Together, these findings provide insight into the genomic landscape of Ewing sarcoma and suggest potential therapeutic targets. For details, please see the article by Crompton, Stewart, and colleagues on page 1326 and the article by Tirode, Surdez, and colleagues on page 1342. - PDF Icon PDF LinkTable of Contents
ISSN 2159-8274
EISSN 2159-8290
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l-2-Hydroxyglutarate: An Epigenetic Modifier and Putative Oncometabolite in Renal Cancer
Eun-Hee Shim; Carolina B. Livi; Dinesh Rakheja; Jubilee Tan; Daniel Benson; Vishwas Parekh; Eun-Young Kho; Arindam P. Ghosh; Richard Kirkman; Sadanan Velu; Shilpa Dutta; Balachandra Chenna; Shane L. Rea; Robert J. Mishur; Qiuhua Li; Teresa L. Johnson-Pais; Lining Guo; Sejong Bae; Shi Wei; Karen Block; Sunil Sudarshan
Brain Tumor Cells in Circulation Are Enriched for Mesenchymal Gene Expression
James P. Sullivan; Brian V. Nahed; Marissa W. Madden; Samantha M. Oliveira; Simeon Springer; Deepak Bhere; Andrew S. Chi; Hiroaki Wakimoto; S. Michael Rothenberg; Lecia V. Sequist; Ravi Kapur; Khalid Shah; A. John Iafrate; William T. Curry; Jay S. Loeffler; Tracy T. Batchelor; David N. Louis; Mehmet Toner; Shyamala Maheswaran; Daniel A. Haber
Research Articles
The Androgen-Regulated Protease TMPRSS2 Activates a Proteolytic Cascade Involving Components of the Tumor Microenvironment and Promotes Prostate Cancer Metastasis
Jared M. Lucas; Cynthia Heinlein; Tom Kim; Susana A. Hernandez; Muzdah S. Malik; Lawrence D. True; Colm Morrissey; Eva Corey; Bruce Montgomery; Elahe Mostaghel; Nigel Clegg; Ilsa Coleman; Christopher M. Brown; Eric L. Schneider; Charles Craik; Julian A. Simon; Antonio Bedalov; Peter S. Nelson
The Genomic Landscape of Pediatric Ewing Sarcoma
Brian D. Crompton; Chip Stewart; Amaro Taylor-Weiner; Gabriela Alexe; Kyle C. Kurek; Monica L. Calicchio; Adam Kiezun; Scott L. Carter; Sachet A. Shukla; Swapnil S. Mehta; Aaron R. Thorner; Carmen de Torres; Cinzia Lavarino; Mariona Suñol; Aaron McKenna; Andrey Sivachenko; Kristian Cibulskis; Michael S. Lawrence; Petar Stojanov; Mara Rosenberg; Lauren Ambrogio; Daniel Auclair; Sara Seepo; Brendan Blumenstiel; Matthew DeFelice; Ivan Imaz-Rosshandler; Angela Schwarz-Cruz y Celis; Miguel N. Rivera; Carlos Rodriguez-Galindo; Mark D. Fleming; Todd R. Golub; Gad Getz; Jaume Mora; Kimberly Stegmaier
Genomic Landscape of Ewing Sarcoma Defines an Aggressive Subtype with Co-Association of STAG2 and TP53 Mutations
Franck Tirode; Didier Surdez; Xiaotu Ma; Matthew Parker; Marie Cécile Le Deley; Armita Bahrami; Zhaojie Zhang; Eve Lapouble; Sandrine Grossetête-Lalami; Michael Rusch; Stéphanie Reynaud; Thomas Rio-Frio; Erin Hedlund; Gang Wu; Xiang Chen; Gaelle Pierron; Odile Oberlin; Sakina Zaidi; Gordon Lemmon; Pankaj Gupta; Bhavin Vadodaria; John Easton; Marta Gut; Li Ding; Elaine R. Mardis; Richard K. Wilson; Sheila Shurtleff; Valérie Laurence; Jean Michon; Perrine Marec-Bérard; Ivo Gut; James Downing; Michael Dyer; Jinghui Zhang; Olivier Delattre; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium; for the St. Jude Children's Research Hospital–Washington University Pediatric Cancer Genome Project and the International Cancer Genome Consortium
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