Please use this identifier to cite or link to this item:
Title: Recurrent inactivating RASA2 mutations in melanoma
Authors: Qutob, Nouar
Keywords: Arrhythmia;Cancer genetics;Melanoma - Genetic aspects
Issue Date: 2016
Abstract: Analysis of 501 melanoma exomes revealed RASA2, encoding a RasGAP, as a tumor-suppressor gene mutated in 5% of melanomas. Recurrent loss-of-function mutations in RASA2 were found to increase RAS activation, melanoma cell growth and migration. RASA2 expression was lost in ≥30% of human melanomas and was associated with reduced patient survival. These findings reveal RASA2 inactivation as a melanoma driver and highlight the importance of Ras GAPs in cancer.
Description: Authors include:Rand Arafeh, Rafi Emmanuel, Alona Keren-Paz, Jason Madore, Abdel Elkahloun, James S. Wilmott, Jared J. Gartner, Antonella Di Pizio, Sabina Winograd-Katz, Sivasish Sindiri, Ron Rotkopf, Ken Dutton-Regester, Peter Johansson, Antonia Pritchard, Nicola Waddell, Victoria K. Hill, Jimmy C. Lin, Yael Hevroni, Steven A. Rosenberg, Javed Khan, Shifra Ben-Dor, Masha Y. Niv, Igor Ulitsky, Graham J Mann, Richard A. Scolyer, Nicholas K. Hayward, and Yardena Samuels
Appears in Collections:Fulltext Publications

Files in This Item:
File Description SizeFormat
emss-65345.pdf666.06 kBAdobe PDFView/Open
Show full item record


checked on Nov 17, 2019

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.