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 in | Nature communications Vol. 7; no. 1; pp. 12601 - 17 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
30.08.2016
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
ISSN | 2041-1723 2041-1723 |
DOI | 10.1038/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. |
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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 |
Author_xml | – sequence: 1 givenname: Vida surname: Chitsazzadeh fullname: Chitsazzadeh, Vida organization: Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center Houston, Department of Dermatology, University of Texas MD Anderson Cancer Center Houston – sequence: 2 givenname: Cristian surname: Coarfa fullname: Coarfa, Cristian organization: Department of Molecular and Cellular Biology, Baylor College of Medicine – sequence: 3 givenname: Jennifer A. surname: Drummond fullname: Drummond, Jennifer A. organization: Human Genome Sequencing Center, Baylor College of Medicine – sequence: 4 givenname: Tri surname: Nguyen fullname: Nguyen, Tri organization: Northwest Diagnostic Clinic – sequence: 5 givenname: Aaron surname: Joseph fullname: Joseph, Aaron organization: Skin and Laser Surgery Associates – sequence: 6 givenname: Suneel surname: Chilukuri fullname: Chilukuri, Suneel organization: Bellaire Dermatology – sequence: 7 givenname: Elizabeth surname: Charpiot fullname: Charpiot, Elizabeth organization: Bellaire Dermatology – sequence: 8 givenname: Charles H. surname: Adelmann fullname: Adelmann, Charles H. organization: Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center Houston, Department of Dermatology, University of Texas MD Anderson Cancer Center Houston – sequence: 9 givenname: Grace surname: Ching fullname: Ching, Grace organization: Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center Houston, Department of Dermatology, University of Texas MD Anderson Cancer Center Houston – sequence: 10 givenname: Tran N. surname: Nguyen fullname: Nguyen, Tran N. organization: Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center Houston – sequence: 11 givenname: Courtney surname: Nicholas fullname: Nicholas, Courtney organization: Department of Translational Molecular Pathology, University of Texas MD 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organization: Next Generation Sequencing Facility, Smithville, University of Texas MD Anderson Cancer Center Houston – sequence: 18 givenname: Kayla surname: McNiece fullname: McNiece, Kayla organization: Department of Dermatology, University of Texas Medical School at Houston – sequence: 19 givenname: Maxim A. surname: Polansky fullname: Polansky, Maxim A. organization: Department of Dermatology, University of Texas Medical School at Houston – sequence: 20 givenname: Hussein A. surname: Abbas fullname: Abbas, Hussein A. organization: Department of Biochemistry and Molecular Biology, University of Texas MD Anderson Cancer Center Houston – sequence: 21 givenname: Kimal surname: Rajapakshe fullname: Rajapakshe, Kimal organization: Department of Molecular and Cellular Biology, Baylor College of Medicine – sequence: 22 givenname: Adam surname: Gower fullname: Gower, Adam organization: Department of Medicine, Boston University School of Medicine – sequence: 23 givenname: Avrum surname: Spira fullname: Spira, Avrum organization: Department of Medicine, Boston University School of Medicine – sequence: 24 givenname: Kyle R. surname: Covington fullname: Covington, Kyle R. organization: Department of Molecular and Cellular Biology, Baylor College of Medicine, Human Genome Sequencing Center, Baylor College of Medicine – sequence: 25 givenname: Weimin surname: Xiao fullname: Xiao, Weimin organization: Department of Biology and Biochemistry University of Houston – sequence: 26 givenname: Preethi surname: Gunaratne fullname: Gunaratne, Preethi organization: Department of Biology and Biochemistry University of Houston – sequence: 27 givenname: Curtis surname: Pickering fullname: Pickering, Curtis organization: Department of Head & Neck Surgery, University of Texas MD Anderson Cancer Center Houston – sequence: 28 givenname: Mitchell surname: Frederick fullname: Frederick, Mitchell organization: Department of Head & Neck Surgery, University of Texas MD Anderson Cancer Center Houston – sequence: 29 givenname: Jeffrey N. surname: Myers fullname: Myers, Jeffrey N. organization: Department of Head & Neck Surgery, University of Texas MD Anderson Cancer Center Houston – sequence: 30 givenname: Li surname: Shen fullname: Shen, Li organization: Department of Bioinformatics & Computational Biology, University of Texas MD Anderson Cancer Center Houston – sequence: 31 givenname: Hui surname: Yao fullname: Yao, Hui organization: Department of Bioinformatics & Computational Biology, University of Texas MD Anderson Cancer Center Houston – sequence: 32 givenname: Xiaoping surname: Su fullname: Su, Xiaoping organization: Department of Bioinformatics & Computational Biology, University of Texas MD Anderson Cancer Center Houston – sequence: 33 givenname: Ronald P. surname: Rapini fullname: Rapini, Ronald P. organization: Department of Dermatology, University of Texas MD Anderson Cancer Center Houston, Department of Dermatology, University of Texas Medical School at Houston – sequence: 34 givenname: David A. surname: Wheeler fullname: Wheeler, David A. organization: Department of Molecular and Cellular Biology, Baylor College of Medicine, Human Genome Sequencing Center, Baylor College of Medicine – sequence: 35 givenname: Ernest T. surname: Hawk fullname: Hawk, Ernest T. organization: Department of Clinical Cancer Prevention, University of Texas MD Anderson Cancer Center Houston – sequence: 36 givenname: Elsa R. surname: Flores fullname: Flores, Elsa R. organization: Department of Biochemistry and Molecular Biology, University of Texas MD Anderson Cancer Center Houston – sequence: 37 givenname: Kenneth Y. surname: Tsai fullname: Tsai, Kenneth Y. email: kytsai@mdanderson.org organization: Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center Houston, Department of Dermatology, University of Texas MD Anderson Cancer Center Houston |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27574101$$D View this record in MEDLINE/PubMed |
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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 |
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