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Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers

OBJECTIVES: Cancer is likely caused by alterations in gene structure or expression. Recently, next generation sequencing has documented mutations in 106 head and neck squamous cell cancer genomes, suggesting several new candidate genes. However, it remains difficult to determine which mutations dire...

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Autores principales: Spiotto, Michael T., Pytynia, Matthew, Liu, Gene-Fu F., Ranck, Mark C., Widau, Ryan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Stilus Optimus 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886108/
https://www.ncbi.nlm.nih.gov/pubmed/24422024
http://dx.doi.org/10.5037/jomr.2013.4101
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author Spiotto, Michael T.
Pytynia, Matthew
Liu, Gene-Fu F.
Ranck, Mark C.
Widau, Ryan
author_facet Spiotto, Michael T.
Pytynia, Matthew
Liu, Gene-Fu F.
Ranck, Mark C.
Widau, Ryan
author_sort Spiotto, Michael T.
collection PubMed
description OBJECTIVES: Cancer is likely caused by alterations in gene structure or expression. Recently, next generation sequencing has documented mutations in 106 head and neck squamous cell cancer genomes, suggesting several new candidate genes. However, it remains difficult to determine which mutations directly contributed to cancer. Here, summarize the animal models which have already validated and may test cancer causing mutations identified by next generation sequencing approaches. MATERIAL AND METHODS: We reviewed the existing literature on genetically engineered mouse models and next generation sequencing (NGS), as it relates to animal models of squamous cell cancers of the head and neck (HNSCC) in PubMed. RESULTS: NSG has identified an average of 19 to 130 distinct mutations per HNSCC specimen. While many mutations likely had biological significance, it remains unclear which mutations were essential to, or "drive," carcinogenesis. In contrast, "passenger" mutations also exist that provide no selection advantage. The genes identified by NGS included p53, RAS, Human Papillomavirus oncogenes, as well as novel genes such as NOTCH1, DICER and SYNE1,2. Animal models of HNSCC have already validated some of these common gene mutations identified by NGS. CONCLUSIONS: The advent of next generation sequencing will provide new leads to the genetic changes occurring in squamous cell cancers of the head and neck. Animal models will enable us to validate these new leads in order to better elucidate the biology of squamous cell cancers of the head and neck.
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spelling pubmed-38861082014-01-13 Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers Spiotto, Michael T. Pytynia, Matthew Liu, Gene-Fu F. Ranck, Mark C. Widau, Ryan J Oral Maxillofac Res Literature Review OBJECTIVES: Cancer is likely caused by alterations in gene structure or expression. Recently, next generation sequencing has documented mutations in 106 head and neck squamous cell cancer genomes, suggesting several new candidate genes. However, it remains difficult to determine which mutations directly contributed to cancer. Here, summarize the animal models which have already validated and may test cancer causing mutations identified by next generation sequencing approaches. MATERIAL AND METHODS: We reviewed the existing literature on genetically engineered mouse models and next generation sequencing (NGS), as it relates to animal models of squamous cell cancers of the head and neck (HNSCC) in PubMed. RESULTS: NSG has identified an average of 19 to 130 distinct mutations per HNSCC specimen. While many mutations likely had biological significance, it remains unclear which mutations were essential to, or "drive," carcinogenesis. In contrast, "passenger" mutations also exist that provide no selection advantage. The genes identified by NGS included p53, RAS, Human Papillomavirus oncogenes, as well as novel genes such as NOTCH1, DICER and SYNE1,2. Animal models of HNSCC have already validated some of these common gene mutations identified by NGS. CONCLUSIONS: The advent of next generation sequencing will provide new leads to the genetic changes occurring in squamous cell cancers of the head and neck. Animal models will enable us to validate these new leads in order to better elucidate the biology of squamous cell cancers of the head and neck. Stilus Optimus 2013-04-01 /pmc/articles/PMC3886108/ /pubmed/24422024 http://dx.doi.org/10.5037/jomr.2013.4101 Text en Copyright © Spiotto MT, Pytynia M, Liu GF, Ranck MC, Widau R. Published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH (http://www.ejomr.org), 1 April 2013. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article, first published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH, distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work and is properly cited. The copyright, license information and link to the original publication on http://www.ejomr.org must be included.
spellingShingle Literature Review
Spiotto, Michael T.
Pytynia, Matthew
Liu, Gene-Fu F.
Ranck, Mark C.
Widau, Ryan
Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title_full Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title_fullStr Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title_full_unstemmed Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title_short Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
title_sort animal models to study the mutational landscape for oral cavity and oropharyngeal cancers
topic Literature Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886108/
https://www.ncbi.nlm.nih.gov/pubmed/24422024
http://dx.doi.org/10.5037/jomr.2013.4101
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