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    • Research Article4

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    • An, Yawen1
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    • Original Article Melanocytes/Melanoma
      Open Access

      Melanocytes Sense Blue Light and Regulate Pigmentation through Opsin-3

      Journal of Investigative Dermatology
      Vol. 138Issue 1p171–178Published online: August 22, 2017
      • Claire Regazzetti
      • Laura Sormani
      • Delphine Debayle
      • Françoise Bernerd
      • Meri K. Tulic
      • Gian Marco De Donatis
      • and others
      Cited in Scopus: 162
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        The shorter wavelengths of the visible light spectrum have been recently reported to induce a long-lasting hyperpigmentation but only in melano-competent individuals. Here, we provide evidence showing that OPN3 is the key sensor in melanocytes responsible for hyperpigmentation induced by the shorter wavelengths of visible light. The melanogenesis induced through OPN3 is calcium dependent and further activates CAMKII followed by CREB, extracellular signal-regulated kinase, and p38, leading to the phosphorylation of MITF and ultimately to the increase of the melanogenesis enzymes: tyrosinase and dopachrome tautomerase.
        Melanocytes Sense Blue Light and Regulate Pigmentation through Opsin-3
      • Original Article Melanocytes/Melanoma
        Open Archive

        Simvastatin Protects Human Melanocytes from H2O2-Induced Oxidative Stress by Activating Nrf2

        Journal of Investigative Dermatology
        Vol. 137Issue 6p1286–1296Published online: February 4, 2017
        • Yuqian Chang
        • Shuli Li
        • Weinan Guo
        • Yuqi Yang
        • Weigang Zhang
        • Qian Zhang
        • and others
        Cited in Scopus: 42
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          The prevention of hydrogen peroxide (H2O2)-induced oxidative stress has proved to be beneficial to vitiligo patients. Simvastatin possesses antioxidative capacity and has shown protective effect in various oxidative stress-related diseases. However, whether simvastatin can protect human melanocytes against oxidative stress has not been investigated. In this study, we initially found that pretreatment with 0.1 μmol/L to 1.0 μmol/L simvastatin led to increased cell viability and decreased cell apoptosis of melanocytes in response to H2O2.
          Simvastatin Protects Human Melanocytes from H2O2-Induced Oxidative Stress by Activating Nrf2
        • Original Article Tumor Biology
          Open Archive

          Yes-Associated Protein Contributes to the Development of Human Cutaneous Squamous Cell Carcinoma via Activation of RAS

          Journal of Investigative Dermatology
          Vol. 136Issue 6p1267–1277Published online: February 20, 2016
          • Jinjing Jia
          • Changji Li
          • Suju Luo
          • Feng Liu-Smith
          • Jiao Yang
          • Xin Wang
          • and others
          Cited in Scopus: 33
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            Cutaneous squamous cell carcinoma (cSCC) is one of the most common skin malignant tumors with an increasing incidence. Studies have shown that Yes-associated protein (YAP) participates in the development of a variety of tumors as an oncogene, but to our knowledge its role in cSCC has not been reported. In this study, we used immunohistochemistry to show that YAP expression was elevated in cSCC samples of different stages versus in normal skin and that it was well correlated with the progression of the disease.
            Yes-Associated Protein Contributes to the Development of Human Cutaneous Squamous Cell Carcinoma via Activation of RAS
          • Original Article Melanocytes/Melanoma
            Open Archive

            The Long Noncoding RNA SPRIGHTLY Regulates Cell Proliferation in Primary Human Melanocytes

            Journal of Investigative Dermatology
            Vol. 136Issue 4p819–828Published online: January 29, 2016
            • Wei Zhao
            • Joseph Mazar
            • Bongyong Lee
            • Junko Sawada
            • Jian-Liang Li
            • John Shelley
            • and others
            Cited in Scopus: 31
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              The long noncoding RNA SPRIGHTLY (formerly SPRY4-IT1), which lies within the intronic region of the SPRY4 gene, is up-regulated in human melanoma cells compared to melanocytes. SPRIGHTLY regulates a number of cancer hallmarks, including proliferation, motility, and apoptosis. To better understand its oncogenic role, SPRIGHTLY was stably transfected into human melanocytes, which resulted in increased cellular proliferation, colony formation, invasion, and development of a multinucleated dendritic-like phenotype.
              The Long Noncoding RNA SPRIGHTLY Regulates Cell Proliferation in Primary Human Melanocytes
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