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 dir...

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Main Authors: Michael T. Spiotto, Matthew Pytynia, Gene-Fu F. Liu, Mark C. Ranck, Ryan Widau
Format: Article
Language:English
Published: Stilus Optimus 2013-01-01
Series:eJournal of Oral Maxillofacial Research
Subjects:
Online Access:http://www.ejomr.org/JOMR/archives/2013/1/e1/v4n1e1ht.htm
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spelling doaj-8fa2635e59dc4df88cbaa1f8971fec652020-11-25T01:40:46ZengStilus OptimuseJournal of Oral Maxillofacial Research2029-283X2013-01-0141e110.5037/jomr.2013.4101Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers Michael T. SpiottoMatthew PytyniaGene-Fu F. LiuMark C. RanckRyan WidauObjectives: 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.http://www.ejomr.org/JOMR/archives/2013/1/e1/v4n1e1ht.htmhead and neck neoplasmspainpostoperativeanalgesicsopioidpain measurementsystematic review.
collection DOAJ
language English
format Article
sources DOAJ
author Michael T. Spiotto
Matthew Pytynia
Gene-Fu F. Liu
Mark C. Ranck
Ryan Widau
spellingShingle Michael T. Spiotto
Matthew Pytynia
Gene-Fu F. Liu
Mark C. Ranck
Ryan Widau
Animal Models to Study the Mutational Landscape for Oral Cavity and Oropharyngeal Cancers
eJournal of Oral Maxillofacial Research
head and neck neoplasms
pain
postoperative
analgesics
opioid
pain measurement
systematic review.
author_facet Michael T. Spiotto
Matthew Pytynia
Gene-Fu F. Liu
Mark C. Ranck
Ryan Widau
author_sort Michael T. Spiotto
title 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_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_sort animal models to study the mutational landscape for oral cavity and oropharyngeal cancers
publisher Stilus Optimus
series eJournal of Oral Maxillofacial Research
issn 2029-283X
publishDate 2013-01-01
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.
topic head and neck neoplasms
pain
postoperative
analgesics
opioid
pain measurement
systematic review.
url http://www.ejomr.org/JOMR/archives/2013/1/e1/v4n1e1ht.htm
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