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dc.contributor.advisorHendry, William J. III
dc.contributor.authorNguyen, Bach
dc.date.accessioned2019-05-10T18:46:21Z
dc.date.available2019-05-10T18:46:21Z
dc.date.issued2019-04-26
dc.identifier.citationNguyen, Bach. 2019. Expression of cancer stem cell marker proteins in pharynx (FaDu) and tongue (CAL27) cell lines of head and neck squamous cell cancer -- In Proceedings: 15th Annual Symposium on Graduate Research and Scholarly Projects. Wichita, KS: Wichita State University
dc.identifier.urihttp://hdl.handle.net/10057/16211
dc.descriptionPresented to the 15th Annual Symposium on Graduate Research and Scholarly Projects (GRASP) held at the Rhatigan Student Center, Wichita State University, April 26, 2019.
dc.descriptionResearch completed in the Department of Biology, Fairmount College of Liberal Arts and Sciences
dc.description.abstractHead and neck cancer is the sixth most common cancer worldwide and its diagnostic rate is approximately 630,000 new patients a year with more than 350,000 deaths every year. The majority (approximately 90%) of head and neck cancers are squamous cell carcinomas (HNSCC) that arise from the stratified squamous epithelial cell lining of the upper aerodigestive tract. The five-year survival rates for HNSCC are relatively low because primary tumor detection at initial stages and relapse prevention has not improved. While some cancer stem cell (CSC) markers are recognized in HNSCC, a complete profile of such markers for possible prognosis and diagnostic purposes is not well established. Additionally, utilization of the hamster cheek pouch xenotransplantation model now appears to be particularly well suited to the analysis of HNSCC cells and tumor tissue samples. Thus, this project assessed the expression of particular cancer stem cell protein markers in two HNSCC cell lines utilizing Western blot and immunohistochemical analyses and then used the hamster cheek xenotransplantation model to examine the in vivo growth potential of those two cell lines. We did detect distinct expression patterns for cancer stem cell marker proteins: Cortactin, HSP60, and Oct-3/4. Furthermore, we did generate two viable xenotransplant masses from one of the HNSCC cell lines. We will next analyze those tissue masses at both the histomorphological and protein expression levels.
dc.description.sponsorshipGraduate School, Academic Affairs, University Libraries
dc.language.isoen_US
dc.publisherWichita State University
dc.relation.ispartofseriesGRASP
dc.relation.ispartofseriesv. 15
dc.titleExpression of cancer stem cell marker proteins in pharynx (FaDu) and tongue (CAL27) cell lines of head and neck squamous cell cancer
dc.typeAbstract
dc.rights.holderWichita State University


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