Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
12788
Cancer Research UK - United Kingdom
336045
European Research Council - International
PubMed
26214592
PubMed Central
PMC4603357
DOI
10.1038/ng.3362
Knihovny.cz E-zdroje
- MeSH
- aktivátorový protein specifický pro B-buňky genetika MeSH
- akutní lymfatická leukemie farmakoterapie genetika mortalita MeSH
- antitumorózní látky farmakologie terapeutické užití MeSH
- chemorezistence MeSH
- exprese genu MeSH
- fúzní onkogenní proteiny genetika metabolismus MeSH
- genetické asociační studie MeSH
- genomika MeSH
- inhibiční koncentrace 50 MeSH
- Kaplanův-Meierův odhad MeSH
- kohortové studie MeSH
- kokultivační techniky MeSH
- lidé MeSH
- mutace MeSH
- mutační analýza DNA MeSH
- myši inbrední NOD MeSH
- myši SCID MeSH
- náhradní lehké řetězce imunoglobulinů genetika MeSH
- sekvenční delece MeSH
- xenogenní modely - testy antitumorózní aktivity MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aktivátorový protein specifický pro B-buňky MeSH
- antitumorózní látky MeSH
- fúzní onkogenní proteiny MeSH
- náhradní lehké řetězce imunoglobulinů MeSH
- PAX5 protein, human MeSH Prohlížeč
- TCF3-HLF fusion protein, human MeSH Prohlížeč
- VPREB1 protein, human MeSH Prohlížeč
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
Children's Cancer Research Institute Vienna Austria
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 Pediatrics Acıbadem University Medical School Ataşehir Istanbul Turkey
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
Sheffield Children's Hospital Sheffield United Kingdom
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