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Part I. Development of a Model System for Studying Nitric Oxide in Tumors: High Nitric Oxide-Adapted Head and Neck Squamous Cell Carcinoma Cell Lines

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Title: Part I. Development of a Model System for Studying Nitric Oxide in Tumors: High Nitric Oxide-Adapted Head and Neck Squamous Cell Carcinoma Cell Lines
Author(s): Yarmolyuk, Yaroslav; Vesper, Benjamin J.; Paradise, William A.; Elseth, Kim M.; Tarjan, Gabor; Haines III, G. K.; Radosevich, James A.
Subject(s): nitric oxide oral cancer
Abstract: The free radical nitric oxide (NO) is over-expressed in many tumors, including head and neck squamous cell carcinomas (HNSCC). However, the role NO plays in tumor pathophysiology is still not well understood. We herein report the development of an in vitro model system which can be used to probe the role of NO in the carcinogenesis of HNSCC. Five HNSCC cell lines were adapted to a high NO (HNO) environment by gradually introducing increasing concentrations of DETA-NONOate, a nitrogen-based NO donor, to cell media. The adaptation process was carried out until a sufficiently high enough donor concentration was reached which enabled the HNO cells to survive and grow, but which was lethal to the original, unadapted (“parent”) cells. The adapted HNO cells exhibited analogous morphology to the parent cells, but grew better than their corresponding parent cells in normal media, on soft agar, and in the presence of hydrogen peroxide, an oxygen-based free radical donor. These results indicate the HNO cell lines are unique and possess biologically different properties than the parent cell lines from which they originated. The HNO/parent cell lines developed herein may be used as a model system to better understand the role NO plays in HNSCC carcinogenesis.
Issue Date: 2011-02
Publisher: Springer Verlag
Citation Info: Yarmolyuk, Y. R., Vesper, B. J., Paradise, W. A., Elseth, K. M., Tarjan, G., Haines, G. K., III, & Radosevich, J. A. 2010. Part I. Development of a model system for studying nitric oxide in tumors: high nitric oxide-adapted head and neck squamous cell carcinoma cell lines. Tumor Biology, 32(1):77-85. DOI: 10.1007/s13277-010-0101-1
Type: Article
Description: Post print version of article may differ from published version. The original publication is available at www.springerlink.com; DOI: 10.1007/s13277-010-0101-1.
URI: http://hdl.handle.net/10027/7761
ISSN: 1423-0380
Sponsor: This work was supported by a VA Merit Review Grant (J.A.R.) and a generous contribution from The Cherry Family Foundation.
Date Available in INDIGO: 2011-05-27
 

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