Cross-species identification of genomic drivers of squamous cell carcinoma development across preneoplastic intermediates

Cutaneous squamous cell carcinoma (cuSCC) comprises 15–20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention,...

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Published inNature communications Vol. 7; no. 1; pp. 12601 - 17
Main Authors Chitsazzadeh, Vida, Coarfa, Cristian, Drummond, Jennifer A., Nguyen, Tri, Joseph, Aaron, Chilukuri, Suneel, Charpiot, Elizabeth, Adelmann, Charles H., Ching, Grace, Nguyen, Tran N., Nicholas, Courtney, Thomas, Valencia D., Migden, Michael, MacFarlane, Deborah, Thompson, Erika, Shen, Jianjun, Takata, Yoko, McNiece, Kayla, Polansky, Maxim A., Abbas, Hussein A., Rajapakshe, Kimal, Gower, Adam, Spira, Avrum, Covington, Kyle R., Xiao, Weimin, Gunaratne, Preethi, Pickering, Curtis, Frederick, Mitchell, Myers, Jeffrey N., Shen, Li, Yao, Hui, Su, Xiaoping, Rapini, Ronald P., Wheeler, David A., Hawk, Ernest T., Flores, Elsa R., Tsai, Kenneth Y.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 30.08.2016
Nature Publishing Group
Nature Portfolio
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Online AccessGet full text
ISSN2041-1723
2041-1723
DOI10.1038/ncomms12601

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Abstract Cutaneous squamous cell carcinoma (cuSCC) comprises 15–20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention, here we perform integrated cross-species genomic analysis of cuSCC development through the preneoplastic AK stage using matched human samples and a solar ultraviolet radiation-driven Hairless mouse model. We identify the major transcriptional drivers of this progression sequence, showing that the key genomic changes in cuSCC development occur in the normal skin to AK transition. Our data validate the use of this ultraviolet radiation-driven mouse cuSCC model for cross-species analysis and demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from diverse sites, suggesting that cuSCC may serve as an effective, accessible model for multiple SCC types and that common treatment and prevention strategies may be feasible. Cutaneous squamous cell of the skin is a common neoplasm that frequently arises from precancerous actinic keratoses. Here, the authors carry out genomic analysis on matched sets of human lesions and compare with those in ultraviolet treated mice and identify conserved drivers of tumour development.
AbstractList Cutaneous squamous cell carcinoma (cuSCC) comprises 15–20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention, here we perform integrated cross-species genomic analysis of cuSCC development through the preneoplastic AK stage using matched human samples and a solar ultraviolet radiation-driven Hairless mouse model. We identify the major transcriptional drivers of this progression sequence, showing that the key genomic changes in cuSCC development occur in the normal skin to AK transition. Our data validate the use of this ultraviolet radiation-driven mouse cuSCC model for cross-species analysis and demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from diverse sites, suggesting that cuSCC may serve as an effective, accessible model for multiple SCC types and that common treatment and prevention strategies may be feasible. Cutaneous squamous cell of the skin is a common neoplasm that frequently arises from precancerous actinic keratoses. Here, the authors carry out genomic analysis on matched sets of human lesions and compare with those in ultraviolet treated mice and identify conserved drivers of tumour development.
Cutaneous squamous cell carcinoma (cuSCC) comprises 15-20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention, here we perform integrated cross-species genomic analysis of cuSCC development through the preneoplastic AK stage using matched human samples and a solar ultraviolet radiation-driven Hairless mouse model. We identify the major transcriptional drivers of this progression sequence, showing that the key genomic changes in cuSCC development occur in the normal skin to AK transition. Our data validate the use of this ultraviolet radiation-driven mouse cuSCC model for cross-species analysis and demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from diverse sites, suggesting that cuSCC may serve as an effective, accessible model for multiple SCC types and that common treatment and prevention strategies may be feasible.
Cutaneous squamous cell of the skin is a common neoplasm that frequently arises from precancerous actinic keratoses. Here, the authors carry out genomic analysis on matched sets of human lesions and compare with those in ultraviolet treated mice and identify conserved drivers of tumour development.
Cutaneous squamous cell carcinoma (cuSCC) comprises 15-20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention, here we perform integrated cross-species genomic analysis of cuSCC development through the preneoplastic AK stage using matched human samples and a solar ultraviolet radiation-driven Hairless mouse model. We identify the major transcriptional drivers of this progression sequence, showing that the key genomic changes in cuSCC development occur in the normal skin to AK transition. Our data validate the use of this ultraviolet radiation-driven mouse cuSCC model for cross-species analysis and demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from diverse sites, suggesting that cuSCC may serve as an effective, accessible model for multiple SCC types and that common treatment and prevention strategies may be feasible.Cutaneous squamous cell carcinoma (cuSCC) comprises 15-20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in association with a distinct precancerous lesion, the actinic keratosis (AK). To identify potential targets for molecularly targeted chemoprevention, here we perform integrated cross-species genomic analysis of cuSCC development through the preneoplastic AK stage using matched human samples and a solar ultraviolet radiation-driven Hairless mouse model. We identify the major transcriptional drivers of this progression sequence, showing that the key genomic changes in cuSCC development occur in the normal skin to AK transition. Our data validate the use of this ultraviolet radiation-driven mouse cuSCC model for cross-species analysis and demonstrate that cuSCC bears deep molecular similarities to multiple carcinogen-driven SCCs from diverse sites, suggesting that cuSCC may serve as an effective, accessible model for multiple SCC types and that common treatment and prevention strategies may be feasible.
ArticleNumber 12601
Author Chitsazzadeh, Vida
Migden, Michael
Nguyen, Tran N.
Nguyen, Tri
Takata, Yoko
Abbas, Hussein A.
Flores, Elsa R.
Spira, Avrum
Polansky, Maxim A.
Adelmann, Charles H.
Ching, Grace
Gunaratne, Preethi
Myers, Jeffrey N.
Gower, Adam
Hawk, Ernest T.
Charpiot, Elizabeth
Thomas, Valencia D.
Su, Xiaoping
Tsai, Kenneth Y.
Nicholas, Courtney
Rajapakshe, Kimal
Frederick, Mitchell
Covington, Kyle R.
Xiao, Weimin
Shen, Li
Yao, Hui
Drummond, Jennifer A.
Rapini, Ronald P.
Chilukuri, Suneel
Joseph, Aaron
Pickering, Curtis
Wheeler, David A.
Shen, Jianjun
Coarfa, Cristian
MacFarlane, Deborah
McNiece, Kayla
Thompson, Erika
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27574101$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright The Author(s) 2016
Copyright Nature Publishing Group Aug 2016
Copyright © 2016, The Author(s) 2016 The Author(s)
Copyright_xml – notice: The Author(s) 2016
– notice: Copyright Nature Publishing Group Aug 2016
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SSID ssj0000391844
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Snippet Cutaneous squamous cell carcinoma (cuSCC) comprises 15–20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in...
Cutaneous squamous cell carcinoma (cuSCC) comprises 15-20% of all skin cancers, accounting for over 700,000 cases in USA annually. Most cuSCC arise in...
Cutaneous squamous cell of the skin is a common neoplasm that frequently arises from precancerous actinic keratoses. Here, the authors carry out genomic...
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SubjectTerms 38
38/39
631/67/1813/1352
631/67/69
64
64/60
Animals
Antineoplastic Agents - therapeutic use
Biochemistry
Biology
Cancer therapies
Carcinogenesis - genetics
Carcinoma, Squamous Cell - etiology
Carcinoma, Squamous Cell - genetics
Carcinoma, Squamous Cell - prevention & control
Dermatology
Disease prevention
Disease Progression
DNA Mutational Analysis
Female
Gene Expression Profiling
Genomes
Genomics
High-Throughput Nucleotide Sequencing
Humanities and Social Sciences
Humans
Keratosis, Actinic - pathology
Medicine
Mice
Mice, Hairless
Molecular Targeted Therapy - methods
multidisciplinary
Precancerous Conditions - genetics
Precancerous Conditions - pathology
Science
Science (multidisciplinary)
Sequence Analysis, RNA
Skin - pathology
Skin Neoplasms - etiology
Skin Neoplasms - genetics
Skin Neoplasms - prevention & control
Solar radiation
Surgery
Ultraviolet radiation
Ultraviolet Rays - adverse effects
Whole Exome Sequencing
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Title Cross-species identification of genomic drivers of squamous cell carcinoma development across preneoplastic intermediates
URI https://link.springer.com/article/10.1038/ncomms12601
https://www.ncbi.nlm.nih.gov/pubmed/27574101
https://www.proquest.com/docview/1814929113
https://www.proquest.com/docview/1815681648
https://pubmed.ncbi.nlm.nih.gov/PMC5013636
https://doaj.org/article/2337471e297249159e9e90238c07490c
Volume 7
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