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Altered telomeres in tumors with ATRX and DAXX mutations
Authors:Heaphy Christopher M  de Wilde Roeland F  Jiao Yuchen  Klein Alison P  Edil Barish H  Shi Chanjuan  Bettegowda Chetan  Rodriguez Fausto J  Eberhart Charles G  Hebbar Sachidanand  Offerhaus G Johan  McLendon Roger  Rasheed B Ahmed  He Yiping  Yan Hai  Bigner Darell D  Oba-Shinjo Sueli Mieko  Marie Suely Kazue Nagahashi  Riggins Gregory J  Kinzler Kenneth W  Vogelstein Bert  Hruban Ralph H  Maitra Anirban  Papadopoulos Nickolas  Meeker Alan K
Institution:Department of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.
Abstract:The proteins encoded by ATRX and DAXX participate in chromatin remodeling at telomeres and other genomic sites. Because inactivating mutations of these genes are common in human pancreatic neuroendocrine tumors (PanNETs), we examined the telomere status of these tumors. We found that 61% of PanNETs displayed abnormal telomeres that are characteristic of a telomerase-independent telomere maintenance mechanism termed ALT (alternative lengthening of telomeres). All of the PanNETs exhibiting these abnormal telomeres had ATRX or DAXX mutations or loss of nuclear ATRX or DAXX protein. ATRX mutations also correlate with abnormal telomeres in tumors of the central nervous system. These data suggest that an alternative telomere maintenance function may operate in human tumors with alterations in the ATRX or DAXX genes.
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