Main field(s) of research, Abstract
The observation on striking parallels between cancer cells and stem cells might lead to fundamental changes in the future therapy against cancer. Tumors that originate from neural crest-derived cells, including melanoma, closely resemble their neural crest origin in the molecular signature, differentiation potential, and ability to migrate and invade host tissues and represent a heterogeneous group of malignancies, accounting for thousands of deaths per year worldwide. Melanoma tissue is often heterogeneous and, in addition to melanocytes, contains cells of other neural crest lineages. We have recently identified the neural crest stem cell transcription factor SOX10 as a new downstream target of oncogenic RAS pathway and demonstrated that SOX10 is instrumental for the development of giant congenital naevi and melanoma. To gain further insight into Sox10-mediated melanoma progression, we plan to concentrate on dissecting the upstream and downstream targets of Sox10 using a combination of in vivo (mouse models of melanoma) and in vitro (human melanoma cell lines) approaches. We also aim at understanding how SOX10 might be involved in mediating resistance to RAS-BRAF-MEK-ERK pathway-targeted drugs in melanoma cells. Another interest of our laboratory is to identify the cellular origin of melanoma using in vivo genetic lineage-tracing analysis of melanoma mouse models.
Main fields of research, key words
Stem cells, in vivo lineage tracing, SOX10, melanoma, neuroblastoma
Special Techniques and Equipment
We use genetically modified mouse models to study cancerogenesis as well as a variety of molecular and cellular biology techniques, in vivo xenotransplantation, FACS analysis, microscopy, immunohistochemistry, stem cell explants and in vitro culture.
Education and Training
We have training opportunities for Master and PhD students. We hold regular journal clubs and group meetings.