The goal oflhis application is to use the zebrafish as a |nodel to dissect the molecular connponents of Foxd3-mediated neural crest (NC) cell survival and migration end to determine if these pathways promote metastasis in NG-derived tumors in vivo. The zebrafish with its close synteny to the human genome and its conserved molecular pathways regulating the development of tissues and organs, Offers a powerful tool with which to conduct such research. We previoulsy identified and characterized a zebrafish foxd3 mutant line that has specific NC ceil survival and migration defects. We also identified the Snai1b transcription factor-as a critical mediator of Foxd3 function. The underlying hypothesis of this applicatipn is that knowledge of the Foxd3 pathway wiII provide an understanding environments, requirement for the metaststasis of NC-derived tumors.
In Aim 1, genetic epistasis and biochemistry will determine if Foxd3 directly activates snai1b expression.
This aim will also will also determine whether Snai 1b inhibits NC apoptosis by repressing the expression of one or more BH3-only genes, and promotes NC migration by repressing cadherin-6 expression .
In Aim 2, a list of genes identified in a microarray screen during the bK99 phase will abe analyzed for thier NC expression pattern and knockdown phenotypes, as well as their ability to rescue NC defects in foxd3 mutant and snai 1b MO-injected embryos.
In Aim 3, foxd3 and snai1b will be expressed in developing NC cells to examine their potential roles in promoting metastasis in established zebrafish NC tumors, including a new model identified during the K99 phase. Rodney Stewart will continue to receive advanced training in genetics, neurobiology and oncology throughout his career. This research proposal is designed to support the candidate as an independent investigator during the first 3 years of a faculty appointment in the Department of Oncology Sciences at the Huntsman Cancer Institute at the University of Utah. Huntsrnan Cancer Institute at the yniyersity of-Utahnd

Public Health Relevance

During nonnal development, cells from the neural tube cetah, activate survival programs and migrate to distant regions of the embryo. This process is similar to way cells behave during metastasis in human cancers. The goal of this application is to find the genes involved in the normal embryonic survival and migration programs and determine if these genes are aberrantly during cancer metastasis. nvolved in the normal embryonic survival and migration programs and determine if these genes are afcferrantlyaetivated during cancer metastasis

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Transition Award (R00)
Project #
4R00NS058608-03
Application #
7874867
Study Section
Special Emphasis Panel (NSS)
Program Officer
Riddle, Robert D
Project Start
2009-07-15
Project End
2012-06-30
Budget Start
2009-07-15
Budget End
2010-06-30
Support Year
3
Fiscal Year
2009
Total Cost
$248,999
Indirect Cost
Name
University of Utah
Department
Pediatrics
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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Bolli, Niccolo; Payne, Elspeth M; Rhodes, Jennifer et al. (2011) cpsf1 is required for definitive HSC survival in zebrafish. Blood 117:3996-4007
Stewart, Rodney A; Lee, Jeong-Soo; Lachnit, Martina et al. (2010) Studying peripheral sympathetic nervous system development and neuroblastoma in zebrafish. Methods Cell Biol 100:127-52
Stewart, Rodney A; Sanda, Takaomi; Widlund, Hans R et al. (2010) Phosphatase-dependent and -independent functions of Shp2 in neural crest cells underlie LEOPARD syndrome pathogenesis. Dev Cell 18:750-62
Jette, C A; Flanagan, A M; Ryan, J et al. (2008) BIM and other BCL-2 family proteins exhibit cross-species conservation of function between zebrafish and mammals. Cell Death Differ 15:1063-72
Smolen, Gromoslaw A; Schott, Benjamin J; Stewart, Rodney A et al. (2007) A Rap GTPase interactor, RADIL, mediates migration of neural crest precursors. Genes Dev 21:2131-6