Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options

. 2015 Sep ; 47 (9) : 1020-1029. [epub] 20150727

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26214592

Grantová podpora
12788 Cancer Research UK - United Kingdom
336045 European Research Council - International

TCF3-HLF-positive acute lymphoblastic leukemia (ALL) is currently incurable. Using an integrated approach, we uncovered distinct mutation, gene expression and drug response profiles in TCF3-HLF-positive and treatment-responsive TCF3-PBX1-positive ALL. We identified recurrent intragenic deletions of PAX5 or VPREB1 in constellation with the fusion of TCF3 and HLF. Moreover somatic mutations in the non-translocated allele of TCF3 and a reduction of PAX5 gene dosage in TCF3-HLF ALL suggest cooperation within a restricted genetic context. The enrichment for stem cell and myeloid features in the TCF3-HLF signature may reflect reprogramming by TCF3-HLF of a lymphoid-committed cell of origin toward a hybrid, drug-resistant hematopoietic state. Drug response profiling of matched patient-derived xenografts revealed a distinct profile for TCF3-HLF ALL with resistance to conventional chemotherapeutics but sensitivity to glucocorticoids, anthracyclines and agents in clinical development. Striking on-target sensitivity was achieved with the BCL2-specific inhibitor venetoclax (ABT-199). This integrated approach thus provides alternative treatment options for this deadly disease.

Alacris Theranostics GmbH Berlin Germany

Childhood Leukaemia Investigation Prague Department of Pediatric Hematology Oncology 2nd Faculty of Medicine Charles University Prague Prague Czech Republic

Children's Cancer Research Institute Vienna Austria

Clinic for Pediatric Oncology Hematology and Clinical Immunology Medical Faculty Heinrich Heine University Düsseldorf Germany

Dahlem Centre for Genome Reseach and Medical Systems Biology Berlin Germany

Department of Algorithmic Bioinformatics Heinrich Heine University Düsseldorf Germany

Department of Computer Science Bonn Rhine Sieg University of Applied Sciences Sankt Augustin Germany

Department of Genetics Hôpital Robert Debré and Paris Diderot University Paris France

Department of Hematology Union Hospital Fujian Medical University Fuzhou China

Department of Pediatric Hemato Immunology Hôpital Robert Debré and Paris Diderot University Paris France

Department of Pediatrics Acıbadem University Medical School Ataşehir Istanbul Turkey

Department of Pediatrics Christian Albrechts University of Kiel and University Medical Center Schleswig Holstein Kiel Germany

Department of Pediatrics Laboratory of Pediatric Hematology Oncology University of Padova Padova Italy

Department of Vertebrate Genomics Max Planck Institute for Molecular Genetics Berlin Germany

European Molecular Biology Laboratory Genome Biology Unit Heidelberg Germany

Federal Office for Radiation Protection Oberschleissheim Germany

Institute of Clinical Molecular Biology Christian Albrechts University of Kiel Kiel Germany

Ludwig Center for Cancer Research University of Lausanne Lausanne Switzerland

Northern Institute of Cancer Research Newcastle University Newcastle upon Tyne United Kingdom

Pediatric Hematology and Oncology Charité University Hospital Berlin Germany

Pediatric Hematology and Oncology Hannover Medical School Hannover Germany

Pediatric Oncology Children's Research Centre University Children's Hospital Zurich Zurich Switzerland

Sheffield Children's Hospital Sheffield United Kingdom

Swiss Institute for Bioinformatics Lausanne Switzerland

Universitäts Kinderspital beider Basel Basel Switzerland

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PubMed

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