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    • Research Article8
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    • Original Article Tumor Biology
      Open Access

      HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion

      Journal of Investigative Dermatology
      Vol. 137Issue 10p2208–2216Published online: June 5, 2017
      • Simone Lanfredini
      • Carlotta Olivero
      • Cinzia Borgogna
      • Federica Calati
      • Kathryn Powell
      • Kelli-Jo Davies
      • and others
      Cited in Scopus: 22
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        β-Human papillomaviruses (HPVs) cause near ubiquitous latent skin infection within long-lived hair follicle (HF) keratinocyte stem cells. In patients with epidermodysplasia verruciformis, β-HPV viral replication is associated with skin keratosis and cutaneous squamous cell carcinoma. To determine the role of HF keratinocyte stem cells in β-HPV-induced skin carcinogenesis, we utilized a transgenic mouse model in which the keratin 14 promoter drives expression of the entire HPV8 early region (HPV8tg).
        HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion
      • Original Article Epidemiology
        Open Archive

        Incidence, Mortality, and Trends of Nonmelanoma Skin Cancer in Germany

        Journal of Investigative Dermatology
        Vol. 137Issue 9p1860–1867Published online: May 6, 2017
        • Ulrike Leiter
        • Ulrike Keim
        • Thomas Eigentler
        • Alexander Katalinic
        • Bernd Holleczek
        • Peter Martus
        • and others
        Cited in Scopus: 109
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          Increasing incidence rates (IRs) of nonmelanoma skin cancer (NMSC) in white populations have been described worldwide. Cancer registry data from the Saarland and Schleswig-Holstein federal states were used to analyze incidence and mortality trends in Germany. Age-standardized rates were compared with crude rates to assess disease burden. Joinpoint regression models were used to estimate annual percentage changes and 95% confidence intervals, allowing us to assess temporal trends between 1970 and 2012.
          Incidence, Mortality, and Trends of Nonmelanoma Skin Cancer in Germany
        • Original Article Epidemiology
          Open Archive

          Cigarette Smoking and the Risks of Basal Cell Carcinoma and Squamous Cell Carcinoma

          Journal of Investigative Dermatology
          Vol. 137Issue 8p1700–1708Published online: April 14, 2017
          • Jean Claude Dusingize
          • Catherine M. Olsen
          • Nirmala P. Pandeya
          • Padmini Subramaniam
          • Bridie S. Thompson
          • Rachel E. Neale
          • and others
          Cited in Scopus: 42
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            Sunlight is the principal environmental risk factor for keratinocyte cancers, but other carcinogens have also been implicated, including tobacco smoke. Findings have been conflicting, however. We investigated associations between cigarette smoking and incidence of basal cell carcinoma (BCC) or squamous cell carcinoma (SCC) in QSkin, a prospective study of skin cancer (N = 43,794). Smoking history was self-reported at baseline; newly diagnosed BCCs and SCCs were ascertained through data linkage and verified by histopathology reports.
            Cigarette Smoking and the Risks of Basal Cell Carcinoma and Squamous Cell Carcinoma
          • Original Article Photobiology
            Open Archive

            NADPH Oxidase-1 Plays a Key Role in Keratinocyte Responses to UV Radiation and UVB-Induced Skin Carcinogenesis

            Journal of Investigative Dermatology
            Vol. 137Issue 6p1311–1321Published online: January 26, 2017
            • Houssam Raad
            • Martin Serrano-Sanchez
            • Ghida Harfouche
            • Walid Mahfouf
            • Doriane Bortolotto
            • Vanessa Bergeron
            • and others
            Cited in Scopus: 36
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              The nicotinamide adenine dinucleotide phosphate oxidase (NOX) family enzymes are involved in several physiological functions. However, their roles in keratinocyte responses to UV radiation have not been clearly elucidated. This study shows that, among other NOX family members, UVB irradiation results in a biphasic activation of NOX1 that plays a critical role in defining keratinocyte fate through the modulation of the DNA damage response network. Indeed, suppression of both bursts of UVB-induced NOX1 activation by using a specific peptide inhibitor of NOX1 (InhNOX1) is associated with increased nucleotide excision repair efficiency and reduction of apoptosis, which is finally translated into decreased photocarcinogenesis.
              NADPH Oxidase-1 Plays a Key Role in Keratinocyte Responses to UV Radiation and UVB-Induced Skin Carcinogenesis
            • Review
              Open Archive

              Cancer Stem Cells in Squamous Cell Carcinoma

              Journal of Investigative Dermatology
              Vol. 137Issue 1p31–37Published online: September 16, 2016
              • Zhe Jian
              • Alexander Strait
              • Antonio Jimeno
              • Xiao-Jing Wang
              Cited in Scopus: 22
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                Cancer stem cells (CSCs) are found in many cancer types, including squamous cell carcinoma (SCC). CSCs initiate cancer formation and are linked to metastasis and resistance to therapies. Studies have revealed that several distinct CSC populations coexist in SCC and that tumor initiation and metastatic potential of these populations can be uncoupled. Therefore, it is critical to understand CSC biology to develop novel CSC-targeted therapies for patients with SCC with poor prognoses. This review compares the properties of CSCs in SCC with normal stem cells in the skin, summarizes current advances and characteristics of CSCs, and considers the challenges for CSC-targeted treatment of SCC.
                Cancer Stem Cells in Squamous Cell Carcinoma
              • Review
                Open Archive

                The Senescence-Associated Secretory Phenotype: Critical Effector in Skin Cancer and Aging

                Journal of Investigative Dermatology
                Vol. 136Issue 11p2133–2139Published online: August 18, 2016
                • Kanad Ghosh
                • Brian C. Capell
                Cited in Scopus: 88
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                  Cellular senescence, a state of stable cell cycle arrest in response to cellular stress, is an indispensable mechanism to counter tumorigenesis by halting the proliferation of damaged cells. However, through the secretion of an array of diverse cytokines, chemokines, growth factors, and proteases known as the senescence-associated secretory phenotype (SASP), senescent cells can paradoxically promote carcinogenesis. Consistent with this, removal of senescent cells delays the onset of cancer and prolongs lifespan in vivo, potentially in part through SASP reduction.
                  The Senescence-Associated Secretory Phenotype: Critical Effector in Skin Cancer and Aging
                • Original Article Epidemiology
                  Open Archive

                  Prevalence of Skin Cancer and Related Skin Tumors in High-Risk Kidney and Liver Transplant Recipients in Queensland, Australia

                  Journal of Investigative Dermatology
                  Vol. 136Issue 7p1382–1386Published online: March 8, 2016
                  • Michelle R. Iannacone
                  • Sudipta Sinnya
                  • Nirmala Pandeya
                  • Nikky Isbel
                  • Scott Campbell
                  • Jonathan Fawcett
                  • and others
                  Cited in Scopus: 34
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                    The increased skin cancer incidence in organ transplant recipients is well-known, but the skin cancer burden at any one time is unknown. Our objective was to estimate the period prevalence of untreated skin malignancy and actinic keratoses in high-risk kidney and liver transplant recipients and to assess associated factors. Organ transplant recipients underwent full skin examinations by dermatologically trained physicians. The proportion of examined organ transplant recipients with histopathologically confirmed skin cancer in the 3-month baseline period was estimated.
                  • Original Article Tumor Biology
                    Open Archive

                    A Model to Predict the Risk of Keratinocyte Carcinomas

                    Journal of Investigative Dermatology
                    Vol. 136Issue 6p1247–1254Published online: February 21, 2016
                    • David C. Whiteman
                    • Bridie S. Thompson
                    • Aaron P. Thrift
                    • Maria-Celia Hughes
                    • Chiho Muranushi
                    • Rachel E. Neale
                    • and others
                    Cited in Scopus: 26
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                      Basal cell and squamous cell carcinomas of the skin are the commonest cancers in humans, yet no validated tools exist to estimate future risks of developing keratinocyte carcinomas. To develop a prediction tool, we used baseline data from a prospective cohort study (n = 38,726) in Queensland, Australia, and used data linkage to capture all surgically excised keratinocyte carcinomas arising within the cohort. Predictive factors were identified through stepwise logistic regression models. In secondary analyses, we derived separate models within strata of prior skin cancer history, age, and sex.
                      A Model to Predict the Risk of Keratinocyte Carcinomas
                    • Original Article Genetics
                      Open Archive

                      Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma

                      Journal of Investigative Dermatology
                      Vol. 136Issue 5p930–937Published online: January 29, 2016
                      • Maryam M. Asgari
                      • Wei Wang
                      • Nilah M. Ioannidis
                      • Jacqueline Itnyre
                      • Thomas Hoffmann
                      • Eric Jorgenson
                      • and others
                      Cited in Scopus: 70
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                        We report a genome-wide association study of cutaneous squamous cell carcinoma conducted among non-Hispanic white members of the Kaiser Permanente Northern California health care system. The study includes a genome-wide screen of 61,457 members (6,891 cases and 54,566 controls) genotyped on the Affymetrix Axiom European array and a replication phase involving an independent set of 6,410 additional members (810 cases and 5,600 controls). Combined analysis of screening and replication phases identified 10 loci containing single-nucleotide polymorphisms (SNPs) with P-values < 5 × 10−8.
                        Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma
                      • Original Article Tumor Biology
                        Open Archive

                        Sustained Akt Activity Is Required to Maintain Cell Viability in Seborrheic Keratosis, a Benign Epithelial Tumor

                        Journal of Investigative Dermatology
                        Vol. 136Issue 3p696–705Published online: December 28, 2015
                        • Victor A. Neel
                        • Kristina Todorova
                        • Jun Wang
                        • Eunjeong Kwon
                        • Minjeong Kang
                        • Qingsong Liu
                        • and others
                        Cited in Scopus: 22
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                          Seborrheic keratoses (SKs) are common benign skin tumors that share many morphological features with their malignant counterpart, squamous cell carcinoma. SKs frequently have acquired oncogenic mutations in the receptor tyrosine kinase/phosphatidylinositol 3-kinase/Akt signaling cascade. We developed a reliable culture system to study SKs in vitro and screened these cells using a library of selective kinase inhibitors to evaluate effects on cell survival. These benign tumors are sensitive to inhibition by ATP-competitive Akt inhibitors, including A-443654 and GSK690693.
                          Sustained Akt Activity Is Required to Maintain Cell Viability in Seborrheic Keratosis, a Benign Epithelial Tumor
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