Melanocytes are pigment-producing cells in the skin that arise from multipotent neural crest cells. The specification of melanocytes requires the activity of a transcription factor called micropthalmia-associated transcription factor (Mitf). In addition to directing formation of melanocytes, the normal functions of Mitf are also linked as a lineage oncogene to the abnormal properties of melanoma. This proposal aims to better understand how to alter melanocyte lineage character and will test the hypothesis that mechanisms that disfavor formation and survival of melanocytes may also inhibit melanoma formation. The vertebrate model organism, Danio rerio (zebrafish), will be used to 1) identify chemicals that inhibit expression of mitf and thus disfavor production of melanocytes and 2) use misexpression of neural crest transcription factors to skew neural crest cells away from the melanocyte lineage or reprogram committed melanocytes to a different but related neural crest lineage (i.e. glial/Schwann cell). In the first approach, a high-throughput chemical genetic screen using ~2280 bioactive compounds is being completed to identify chemicals that specifically decrease mitf expression in developing zebrafish embryos. Compounds that reproducibly decrease mitf expression will be assayed for their effects on neural crest stem cells, precursors, and committed descendants (e.g. glial, neural, cartilage) to determine where in neural crest development each acts. Based on the likely mechanism of action of mitf-inhibitory compounds, standard gain- and loss-of-function approaches in the zebrafish will be used to establish the regulatory mechanism(s) affecting mitf expression. In the second approach, the lineage identity of developing and committed melanocytes will be altered in zebrafish by forcing expression of transcription factors linked to the formation of the adjacent Schwann cell neural crest lineage. Transcription factors shown to skew away from melanocytes during development or to reprogram committed melanocytes will be tested in combination with the identified mitf-inhibitory compounds in a zebrafish melanoma model for their ability to prevent formation and/or cause regression of de novo melanoma tumors. Dr. Kaufman is a clinical fellow in adult oncology at the Dana Farber Cancer Institute (DFCI) and will perform his research project in the laboratory of noted stem cell biologist, Dr. Leonard Zon, in the Division of Hematology/Oncology at the Children's Hospital Boston (CHB). Building on his experience studying mechanisms of transcriptional regulation in the epidermis in mice and humans, Dr. Kaufman will expand his scientific and technical training to studies of lineage regulation in melanocytes and the neural crest using the zebrafish model. Dr. Zon's proven mentorship coupled with the rigorous and nurturing scientific environment offered by the research community at CHB and affiliated institutions offer the maximal opportunity for Dr. Kaufman's success during the award period as a fellow and in his transition to an independent investigator.
Pigment-producing cells in the skin (melanocytes) produce the most deadly form of skin cancer (melanoma) when their growth becomes uncontrolled. Using the zebrafish as a model organism, I will use drug-like chemicals and proteins that control gene expression to inhibit melanocyte formation, which may also prevent or treat melanoma.
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|Kong, Yawei; Grimaldi, Michael; Curtin, Eugene et al. (2014) Neural crest development and craniofacial morphogenesis is coordinated by nitric oxide and histone acetylation. Chem Biol 21:488-501|
|Yen, Jennifer; White, Richard M; Wedge, David C et al. (2013) The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models. Genome Biol 14:R113|