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Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1
BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is an aggressive and lethal malignancy. Publically available cell lines are mostly of lingual origin, or have not been carefully characterized. Detailed characterization of novel HNSCC cell lines is needed in order to provide researchers a co...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841166/ https://www.ncbi.nlm.nih.gov/pubmed/20175927 http://dx.doi.org/10.1186/1758-3284-2-5 |
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author | Liebertz, Daniel J Lechner, Melissa G Masood, Rizwan Sinha, Uttam K Han, Jing Puri, Raj K Correa, Adrian J Epstein, Alan L |
author_facet | Liebertz, Daniel J Lechner, Melissa G Masood, Rizwan Sinha, Uttam K Han, Jing Puri, Raj K Correa, Adrian J Epstein, Alan L |
author_sort | Liebertz, Daniel J |
collection | PubMed |
description | BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is an aggressive and lethal malignancy. Publically available cell lines are mostly of lingual origin, or have not been carefully characterized. Detailed characterization of novel HNSCC cell lines is needed in order to provide researchers a concrete keystone on which to build their investigations. METHODS: The USC-HN1 cell line was established from a primary maxillary HNSCC biopsy explant in tissue culture. The immortalized cells were then further characterized by heterotransplantation in Nude mice; immunohistochemical staining for relevant HNSCC biomarkers; flow cytometry for surface markers; cytogenetic karyotypic analysis; human papillomavirus and Epstein-Barr virus screening; qRT-PCR for oncogene and cytokine analysis; investigation of activated, cleaved Notch1 levels; and detailed 35,000 gene microarray analysis. RESULTS: Characterization experiments confirmed the human HNSCC origin of USC-HN1, including a phenotype similar to the original tumor. Viral screening revealed no HPV or EBV infection, while western blotting displayed significant upregulation of activated, cleaved Notch1. CONCLUSIONS: USC-HN1, a novel immortalized cell line has been derived from a maxillary HNSCC. Characterization studies have shown that the cell line is of HNSCC origin and displays many of the same markers previously reported in the literature. USC-HN1 is available for public research and will further the investigation of HNSCC and the development of new therapeutic modalities. |
format | Text |
id | pubmed-2841166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28411662010-03-18 Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 Liebertz, Daniel J Lechner, Melissa G Masood, Rizwan Sinha, Uttam K Han, Jing Puri, Raj K Correa, Adrian J Epstein, Alan L Head Neck Oncol Research BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is an aggressive and lethal malignancy. Publically available cell lines are mostly of lingual origin, or have not been carefully characterized. Detailed characterization of novel HNSCC cell lines is needed in order to provide researchers a concrete keystone on which to build their investigations. METHODS: The USC-HN1 cell line was established from a primary maxillary HNSCC biopsy explant in tissue culture. The immortalized cells were then further characterized by heterotransplantation in Nude mice; immunohistochemical staining for relevant HNSCC biomarkers; flow cytometry for surface markers; cytogenetic karyotypic analysis; human papillomavirus and Epstein-Barr virus screening; qRT-PCR for oncogene and cytokine analysis; investigation of activated, cleaved Notch1 levels; and detailed 35,000 gene microarray analysis. RESULTS: Characterization experiments confirmed the human HNSCC origin of USC-HN1, including a phenotype similar to the original tumor. Viral screening revealed no HPV or EBV infection, while western blotting displayed significant upregulation of activated, cleaved Notch1. CONCLUSIONS: USC-HN1, a novel immortalized cell line has been derived from a maxillary HNSCC. Characterization studies have shown that the cell line is of HNSCC origin and displays many of the same markers previously reported in the literature. USC-HN1 is available for public research and will further the investigation of HNSCC and the development of new therapeutic modalities. BioMed Central 2010-02-22 /pmc/articles/PMC2841166/ /pubmed/20175927 http://dx.doi.org/10.1186/1758-3284-2-5 Text en Copyright ©2010 Liebertz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Liebertz, Daniel J Lechner, Melissa G Masood, Rizwan Sinha, Uttam K Han, Jing Puri, Raj K Correa, Adrian J Epstein, Alan L Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title | Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title_full | Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title_fullStr | Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title_full_unstemmed | Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title_short | Establishment and Characterization of a Novel Head and Neck Squamous Cell Carcinoma Cell Line USC-HN1 |
title_sort | establishment and characterization of a novel head and neck squamous cell carcinoma cell line usc-hn1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841166/ https://www.ncbi.nlm.nih.gov/pubmed/20175927 http://dx.doi.org/10.1186/1758-3284-2-5 |
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