Director of the Flow Cytometry Core
Department: Biochemistry and Molecular Biology
Research Clusters: Cancer Biology; Infectious and Immunological Diseases
Office: BBSC 336-N | Laboratories: BBSC 313 and 323
Phone: (304) 696-7357 | Fax: (304) 696-7207
Link to Dr. Sollars’ CV
The Question: “What are the processes that enable a normal cell to start misbehaving and become cancer cells?” The process that cells in our bodies undergo to become cancer cells all end up producing a cell that ceases to listen and cooperate with its neighbors, which is necessary for the complex mixture of cell our bodies are. This grant will investigate a process known as “canalization”, which much like a canal for water directs the flow of water, directs a cell as it matures to the necessary type of cell the body requires. Disrupting this “canalization” process can cause a cell to change and lose its direction, potentially pushing it down paths that lead to cancer.
Research Goals: The research will use both cells grown in the laboratory and animal models of human leukemia, along with advanced scientific methods to test the role of canalization in the process of maturing cells and cancer development. The research will allow students at Marshall University the opportunity to participate in cutting edge research in preparation for careers in science.
Benefit: This highly innovative proposal can have a great impact on how canalization drives cancer. Our increased understanding of this process in cancer progression will facilitate the development of new combinatorial therapeutic strategies for most cancers.
EML cell model system: We have obtained the EML cell line from its creator Dr. Tsai. EML cells are a suspended hematopoietic stem cell (HSC) line comprising mostly blast appearing cells that can be induced to differentiate into myeloid or lymphoid cells. This cell line is stem cell factor dependent and has been immortalized by over expression of a dominant-negative retinoic acid receptor. Here, EML cells have been induced to differentiate into macrophages and granulocytes by addition of appropriate cytokines.
Canalization of acquired characteristics: The expression patterns of genes from one organism to the next in a particular species are diverse enough to give a wide range of phenotypes that are not present in the population (depicted on the left with a y-axis of phenotypic range). Additionally, the predominant success of the complex process of development despite high precision in cell fate decisions and spatial relationships suggests a mechanism for buffering for minor changes. Canalization theory states that this is the result of canalization of the preferred normal phenotype of the species during development. The present morphology of the species is favored and variations in gene expression that would result in deviation from this model are compensated for by canalizers (or capacitors) present in the system. Similar to how canals direct water, the process of canalization directs the maturation of cells to their proper cell fates.
Loss of Canalization: This diagram shows the potential ramification of the loss of canalization on cancer progression. Here we show the ability of the known oncogene WNT, which is a cell secreted signaling molecule shown as an orange dot, to stimulate cells. Loss of canalization could affect the gene expression level of the know negative regulator of WNT signaling. SFRPs, to repress this signal transduction cascade by sequestration of the ligand in the extracellular matrix. Loss of canalization would produce greater variance in the secretion of SFRPs, producing cells with high levels that are refractory to WNT signaling and cells of low levels that would be easily stimulated by WNT signaling and prone to over-stimulation.
Macrophages and Pseudomonas: Epifluorescent images of naïve macrophages produced from bone marrow progenitor cells harvested from mice after a 20 minute exposure to P. aeruginosa. The nuclei are stained red with ethidium bromide, while the endoplasmic reticulum is stained blue with ER-Tracker™ Blue-White DPX and the bacteria appear green due to GFP expression (white arrows).
Xiangyi Lu, Luan Wang, Vincent E. Sollars, Mark Garfinkel, and Douglas M. Ruden (2013). Hsp90 as a Capacitor of Both Genetic and Epigenetic Changes in the Genome During Cancer Progression and Evolution. Stress-Induced Mutagenesis. Ed. Mittleman, David. New York, NY, Springer. ISBN 978-1-4614-6280-4
Vincent E. Sollars (2012). Epigenetics as a Mechanism for Dietary Fatty Acids to Affect Hematopoietic Stem/Progenitor Cells and Leukemia – Royal Jelly for the Blood. Nutrition and Cancer, from Epidemiology to Biology. Eds: Pier Paolo Claudio and Richard M. Niles. Brussels, Belgium, Bentham Science Publishers. pp. 65-76. eISBN: 978-1-60805-447-3, 2012
Domain requirements for the diverse immune regulatory functions of foxp3 (2011). Wei-ping Zeng, Vincent E. Sollars, and Andrea Del Pilar Belalcazar. Molecular Immunology 48, 1932-1939. PMID: 21737139.
YB-1 expression and function in early hematopoiesis (2011). Jasjeet Bhullar and Vincent E. Sollars. Immunogenetics 63, 337-350. PMID:21369783.
A high omega-3 fatty acid diet has different effects on early and late stage myeloid progenitors (2011). Melinda E. Varney, James T. Buchanan, Yulia Dementieva, W. Elaine Hardman and Vincent E. Sollars. Lipids 46(1), 47-57. PMID: 21038084.