DNMT3A mutations promote anthracycline resistance in acute myeloid leukemia via impaired nucleosome remodeling

被引:0
作者
Olga A Guryanova
Kaitlyn Shank
Barbara Spitzer
Luisa Luciani
Richard P Koche
Francine E Garrett-Bakelman
Chezi Ganzel
Benjamin H Durham
Abhinita Mohanty
Gregor Hoermann
Sharon A Rivera
Alan G Chramiec
Elodie Pronier
Lennart Bastian
Matthew D Keller
Daniel Tovbin
Evangelia Loizou
Abby R Weinstein
Adriana Rodriguez Gonzalez
Yen K Lieu
Jacob M Rowe
Friederike Pastore
Anna Sophia McKenney
Andrei V Krivtsov
Wolfgang R Sperr
Justin R Cross
Christopher E Mason
Martin S Tallman
Maria E Arcila
Omar Abdel-Wahab
Scott A Armstrong
Stefan Kubicek
Philipp B Staber
Mithat Gönen
Elisabeth M Paietta
Ari M Melnick
Stephen D Nimer
Siddhartha Mukherjee
Ross L Levine
机构
[1] Human Oncology and Pathogenesis Program,Department of Pediatrics
[2] Memorial Sloan Kettering Cancer Center,Division of Hematology and Oncology, Department of Medicine
[3] Memorial Sloan Kettering Cancer Center,Department of Hematology
[4] University of Miami Sylvester Comprehensive Cancer Center,Department of Laboratory Medicine
[5] Center for Epigenetics Research,Division of Hematology and Hemostaseology
[6] Memorial Sloan Kettering Cancer Center,Department of Physiology and Biophysics and the Institute for Computational Biomedicine
[7] Cancer Biology and Genetics Program,Department of Medicine
[8] Memorial Sloan Kettering Cancer Center,Department of Epidemiology and Biostatistics
[9] Weill Cornell Medicine,Department of Oncology
[10] Shaare Zedek Medical Center,undefined
[11] Diagnostic Molecular Pathology Laboratory,undefined
[12] Memorial Sloan Kettering Cancer Center,undefined
[13] Medical University of Vienna,undefined
[14] Irving Cancer Research Center,undefined
[15] Columbia University,undefined
[16] Comprehensive Cancer Center Vienna,undefined
[17] Medical University of Vienna,undefined
[18] Donald B. and Catherine C. Marron Cancer Metabolism Center,undefined
[19] Memorial Sloan Kettering Cancer Center,undefined
[20] Weill Cornell Medical College of Cornell University,undefined
[21] Leukemia Service,undefined
[22] Memorial Sloan Kettering Cancer Center,undefined
[23] Center for Hematologic Malignancies,undefined
[24] Memorial Sloan Kettering Cancer Center,undefined
[25] Christian Doppler Laboratory for Chemical Genetics and Anti-Infectives,undefined
[26] CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences,undefined
[27] Memorial Sloan Kettering Cancer Center,undefined
[28] Montefiore Medical Center,undefined
来源
Nature Medicine | 2016年 / 22卷
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学科分类号
摘要
AML cells carrying R882 mutations in DNMT3A fail to sense and repair DNA damage induced by standard-dose chemotherapy as a result of impaired chromatin remodeling
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页码:1488 / 1495
页数:7
相关论文
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[1]  
Ley TJ(2010)DNMT3A mutations in acute myeloid leukemia N. Engl. J. Med. 363 2424-2433
[2]  
Yan XJ(2011)Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia Nat. Genet. 43 309-315
[3]  
Genovese G(2014)Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence N. Engl. J. Med. 371 2477-2487
[4]  
Jaiswal S(2014)Age-related clonal hematopoiesis associated with adverse outcomes N. Engl. J. Med. 371 2488-2498
[5]  
Patel JP(2012)Prognostic relevance of integrated genetic profiling in acute myeloid leukemia N. Engl. J. Med. 366 1079-1089
[6]  
Sehgal AR(2015)DNMT3A mutational status affects the results of dose-escalated induction therapy in acute myelogenous leukemia Clin. Cancer Res. 21 1614-1620
[7]  
Shlush LI(2014)Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia Nature 506 328-333
[8]  
Leiserson MD(2015)Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes Nat. Genet. 47 106-114
[9]  
Welch JS(2012)The origin and evolution of mutations in acute myeloid leukemia Cell 150 264-278
[10]  
Busque L(2012)Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis Nat. Genet. 44 1179-1181