Research
- Research Topics
- Cell Biology and Tumor Biology
- Stem Cells and Cancer
- Inflammatory Stress in Stem Cells
- Experimental Hematology
- Molecular Embryology
- Signal Transduction and Growth Control
- Epigenetics
- Redox Regulation
- Vascular Oncology and Metastasis
- Clinical Neurobiology
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- Vascular Signaling and Cancer
- Molecular Neurobiology
- Mechanisms Regulating Gene Expression
- Molecular Biology of Centrosomes and Cilia
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- Pediatric Leukemia
- Tumour Metabolism and Microenvironment
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- Molecular Hematology - Oncology
- Cancer Progression and Metastasis
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- Cell Signaling and Metabolism
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- Cancer Drug Development
- Cell Morphogenesis and Signal Transduction
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- Pediatric Neurooncology
- Cancer Genome Research
- Chromatin Networks
- Functional Genome Analysis
- Theoretical Systems Biology
- Neuroblastoma Genomics
- Signaling and Functional Genomics
- Signal Transduction in Cancer and Metabolism
- RNA Biology and Cancer
- Systems Biology of Signal Transduction
- Areas of Interest
- Advancement of clinical proteomics for systems medicine
- Bridging from the single cell to the cell population – Epo-induced cellular responses and erythroleukemia
- Deciphering tumor microenvironment interactions determining lung cancer development
- Mechanisms controlling the compensation of liver injury and towards model-based biomarkers for early detection of liver cancer
- Application of dynamic pathway modelling for personalized medicine
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- Molecular thoracic Oncology
- Proteomics of Stem Cells and Cancer
- Computational Genomics and System Genetics
- Applied Functional Genomics
- Applied Bioinformatics
- Translational Medical Oncology
- Metabolic crosstalk in cancer
- Pediatric Glioma Research
- Cancer Epigenomics
- Translational Pediatric Sarcoma Research
- Artificial Intelligence in Oncology
- Mechanisms of Genomic Variation and Data Science
- Neuropathology
- Pediatric Oncology
- Neurooncology
- Somatic Evolution and Early Detection
- Translational Control and Metabolism
- Soft-Tissue Sarcoma
- Precision Sarcoma Research
- Brain Mosaicism and Tumorigenesis
- Mechanisms of Genome Control
- Translational Gastrointestinal Oncology and Preclinical Models
- Translational Lymphoma Research
- Mechanisms of Leukemogenesis
- Genome Instability in Tumors
- Developmental Origins of Pediatric Cancer
- Brain Tumor Translational Targets
- Translational Functional Cancer Genomics
- Regulatory Genomics and Cancer Evolution
- SPRINT
- Cancer Risk Factors and Prevention
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- Clinical Epidemiology and Aging Research
- Health Economics
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- Preventive Oncology
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- Digital Biomarkers for Oncology
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- Molecular Oncology of Gastrointestinal Tumors
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- Multiparametric methods for early detection of prostate cancer
- Molecular Mechanisms of Head and Neck Tumors
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- Experimental Hepatology, Inflammation and Cancer
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Developmental specification of adult stem cells and the study of how key biological processes differ in these cells between the embryonic and adult state
During embryonic development, HSCs are generated from pluripotent cells in a series of progressive differentiation steps. This process can be modeled in vitro by directing the differentiation of pluripotent cell lines, such as embryonic stem (ES) cells or induced pluripotent stem cells (iPSCs), towards the formation of the hematopoietic lineages. The in vitro specification of hematopoietic lineages from ES cells and patient-specific iPSCs closely mimics the process via which HSCs are generated during development, and holds enormous potential for disease modeling and for the eventual scalable production of differentiated cells for regenerative therapy. However, a number of differences exist between the normal developmental process and the in vitro differentiation procedure. The most notable of these differences is the current inability to generate in vitro, HSCs that have the same functional properties as their in vivo specified counterparts. One of the current focuses of the Experimental Hematology group is to better understand the important molecular and biological differences between hematopoietic specification in vitro and in vivo, and to attempt to apply this knowledge towards developing better methodologies for the generation of functional HSCs from ES cells and iPSCs.
Key Publications on pluripotent cell lines and HSC specification
- §Müller L.U.W., §Milsom M.D., Harris C.E., Vyas R., Brumme K.M., Parmar K., Moreau L.A., Schambach A., Park I.H., London W.B., Strait K., D’Andrea A., Daley G.Q. and Williams D.A. (2012). Overcoming reprogramming resistance of Fanconi anemia cells. Blood. 119 (23): pp5449-57. §Equal contribution.
- Ghiaur G., Ferkowicz M.J., Milsom M.D., Bailey J., Cancelas J.A., Yoder M.C. and Williams D.A. (2008). Rac1 is essential for intraembryonic hematopoiesis and for the initial seeding of the fetal liver with hematopoietic progenitor cells. Blood, 111 (7): pp3313-21.