RD3 loss dictates high-risk aggressive neuroblastoma and poor clinical outcomes

Autor: Faizan Haider Khan, Natarajan Aravindan, Vijayabaskar Pandian, Terence S. Herman, Mohan Natarajan, Sheeja Aravindan, Satish Kumar Ramraj, Seifollah Azadi
Rok vydání: 2015
Předmět:
Zdroj: Oncotarget
ISSN: 1949-2553
DOI: 10.18632/oncotarget.5204
Popis: // Faizan H. Khan 1, * , Vijayabaskar Pandian 1, * , Satish Kumar Ramraj 1, * , Sheeja Aravindan 2 , Mohan Natarajan 3 , Seifollah Azadi 4 , Terence S. Herman 1, 2 , Natarajan Aravindan 1 1 Department of Radiation Oncology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA 2 Stephenson Cancer Center, Oklahoma City, OK, USA 3 Department of Pathology, University of Texas Health Sciences Center at San Antonio, San Antonio, TX, USA 4 Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA * These authors have contributed equally to this work Correspondence to: Natarajan Aravindan, e-mail: naravind@ouhsc.edu Keywords: RD3, neuroblastoma, tumor suppressor, high-risk aggressive neuroblastoma, metastasis Received: July 28, 2015 Accepted: August 28, 2015 Published: September 08, 2015 ABSTRACT Clinical outcomes for high-risk neuroblastoma patients remains poor, with only 40–50% 5-Year overall survival (OS) and
Databáze: OpenAIRE