One of the most devastating diseases to manage is metastatic melanoma, where the evidence of stem cell subpopulations is starting to emerge. Comparative global gene analyses of aggressive human melanoma cell lines and tumors have revealed the expression of genes associated with multiple cellular phenotypes and precursor stem cells. These findings support the premise that aggressive melanoma cells revert to a multipotent, plastic phenotype. Key to identifying the molecular mechanisms underlying tumor cell plasticity is to elucidate the unique role the microenvironment plays in this process. Most noteworthy are the data we have generated showing the reprogramming of subpopulations (possibly the stem cells) of multipotent metastatic melanoma cells to a melanocyte-like phenotype by the embryonic microenvironment(s) of hESCs and chick neural crest-rich regions. Based on these observations, we propose to test the central hypothesis that the embryonic microenvironments associated with hESCs (Wa01. Wa09 and UC06) and chick neural crest-rich region(s) - contain informational cues with the potential to epigenetically reprogram the genotype and phenotype of human metastatic multipotent melanoma cells exposed to them. Our long term goal is to understand the biological mechanisms underlying the bi-directional communication between stem cells and their microenvironment(s) that ultimately result in cell fate determinations. Our short term goal is to identify the biological and molecular parameters associated with the epigenetic reprogramming of multipotent metastatic melanoma cells exposed to specific hESC environmental cues. Using unique, 3-D organotypic models and chick embryos, together with functional analysis, 4-D imaging, laser capture microdissection, and epigenetic analysis, we propose to: Unchanged Aim 1: Determine the epigenetic influence of the 3-D microenvironment(s) of hESCs for their potential to reprogram the genotype and phenotype of human metastatic multipotent melanoma cells. Revised Aim 2: Identify the molecular basis for the epigenetic reprogramming of the genotype and phenotype of the affected multipotent melanoma cell populations exposed to various hESC 3-D microenvironments, with particular focus on the Nodal signaling pathway. Revised Aim 3: Investigate the developmental plasticity of multipotent melanoma cell populations in an embryonic chick model - to determine the biological relevance of the Nodal signaling pathway involved in stem cell plasticity and the control of cell fate determination and reprogramming of the metastatic phenotype. Lay Summary: At the completion of these studies, we expect to gain new insights into the biological properties of human embryonic and multipotent metastatic melanoma cells with stem cell properties that could be translated for novel therapeutic applications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA121205-04
Application #
7860642
Study Section
Tumor Microenvironment Study Section (TME)
Program Officer
Mohla, Suresh
Project Start
2007-07-03
Project End
2012-05-31
Budget Start
2010-06-01
Budget End
2011-05-31
Support Year
4
Fiscal Year
2010
Total Cost
$330,969
Indirect Cost
Name
Children's Memorial Hospital (Chicago)
Department
Type
DUNS #
074438755
City
Chicago
State
IL
Country
United States
Zip Code
60611
Margaryan, Naira V; Seftor, Elisabeth A; Seftor, Richard E B et al. (2017) Targeting the Stem Cell Properties of Adult Breast Cancer Cells: Using Combinatorial Strategies to Overcome Drug Resistance. Curr Mol Biol Rep 3:159-164
Margaryan, Naira V; Gilgur, Alina; Seftor, Elisabeth A et al. (2016) Melanocytes Affect Nodal Expression and Signaling in Melanoma Cells: A Lesson from Pediatric Large Congenital Melanocytic Nevi. Int J Mol Sci 17:418
Strizzi, Luigi; Margaryan, Naira V; Gerami, Pedram et al. (2016) Translational significance of Nodal, Cripto-1 and Notch4 in adult nevi. Oncol Lett 12:1349-1354
Bodenstine, Thomas M; Chandler, Grace S; Seftor, Richard E B et al. (2016) Plasticity underlies tumor progression: role of Nodal signaling. Cancer Metastasis Rev 35:21-39
Focà, Annalia; Sanguigno, Luca; Focà, Giuseppina et al. (2015) New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding. Int J Mol Sci 16:21342-62
Strizzi, Luigi; Sandomenico, Annamaria; Margaryan, Naira V et al. (2015) Effects of a novel Nodal-targeting monoclonal antibody in melanoma. Oncotarget 6:34071-86
Khalkhali-Ellis, Zhila; Kirschmann, Dawn A; Seftor, Elisabeth A et al. (2015) Divergence(s) in nodal signaling between aggressive melanoma and embryonic stem cells. Int J Cancer 136:E242-51
Hardy, Katharine M; Strizzi, Luigi; Margaryan, Naira V et al. (2015) Targeting nodal in conjunction with dacarbazine induces synergistic anticancer effects in metastatic melanoma. Mol Cancer Res 13:670-80
Kirsammer, Gina; Strizzi, Luigi; Margaryan, Naira V et al. (2014) Nodal signaling promotes a tumorigenic phenotype in human breast cancer. Semin Cancer Biol 29:40-50
Malchenko, Sergey; Xie, Jianping; de Fatima Bonaldo, Maria et al. (2014) Onset of rosette formation during spontaneous neural differentiation of hESC and hiPSC colonies. Gene 534:400-7

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