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MrgprF Acts as a Tumor Suppressor in Cutaneous Melanoma by Restraining PI3K/Akt Signaling | Scientists identified that MrgprF, a MAS-related GPR family member, was decreased in cutaneous melanoma (CM) tissues and cell lines due to hypermethylation of its promoter region, and showed that patients with CM expressing high levels of MrgprF exhibited an improved clinical outcome. [Signal Transduction and Targeted Therapy] |
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| PUBLICATIONSRanked by the impact factor of the journal |
| DERMAL STEM CELLS & TISSUE REGENERATION |
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Age-Related Decrease in Responsiveness of CD271-Positive Skin Stem Cells to Growth Factors | Investigators focused on epidermal growth factor/epidermal growth factor receptor signaling and fibroblast growth factor-2/fibroblast growth factor receptor signaling and analyzed the age-related changes. [Experimental Dermatology] |
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Chronic Arsenic Exposure Suppresses ATM Pathway Activation in Human Keratinocytes | Researchers reported that phosphorylation of ataxia telengectasia mutated (ATM) protein at a critical site important for DNA damage response signaling, and downstream CHEK2 activation, were significantly reduced in two human keratinocyte lines as a result of chronic inorganic arsenic exposure. [Toxicology and Applied Pharmacology] |
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Large-Scale Isolation of Functional Dermal Papilla Cells Using Novel Surface Marker LEPR | The authors systematically screened for the surface proteins specifically expressed in skin dermal papilla using mRNA expression databases. [Cytometry Part A] |
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Chrna5 Is Overexpressed in Psoriasis Patients and Promotes Psoriasis-Like Inflammation in Mouse Models | Scientists examined the role of cholinergic receptor nicotinic subunit alpha-5 (Chrna5) in psoriasis development and pathogenesis. Human keratinocytes were analyzed, and silencing Chrna5 inhibited keratinocyte proliferation and migration. [Journal of Investigative Dermatology] |
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Transglutaminase 3 Attenuates Skin Inflammation in Psoriasis by Inhibiting NF-κB Activation via P-STAT3–TET3 Signaling | Researchers showed that transglutaminase 3 expression was increased in skin lesions of psoriasis patients and a mouse model of imiquimod-induced psoriatic dermatitis. [Journal of Investigative Dermatology] |
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Inhibition of Bromodomain Extraterminal Histone Readers Alleviates Skin Fibrosis in Experimental Models of Scleroderma | Investigators determined the antifibrotic efficacy and potential mechanisms of bromodomain and extraterminal domain proteins inhibition in systemic sclerosis. [JCI Insight] |
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Nuclear Focal Adhesion Kinase Induces APC/C Activator Protein CDH1-Mediated Cyclin-Dependent Kinase4/6 Degradation and Inhibits Melanoma Proliferation | The authors found that focal adhesion kinase (FAK) played a key role in cell cycle progression potentially through regulation of cyclin-dependent kinase 4/6 protein expression and showed that FAK inhibition increased its nuclear localization and induced G1 arrest in B16F10 melanoma cells. [Journal of Biological Chemistry] |
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Enhanced Expression of p21 Promotes Sensitivity of Melanoma Cells towards Targeted Therapies | Researchers unraveled the role of the p53 target gene CDKN1A/p21 in the response of melanoma cells towards BRAF inhibitor. [Experimental Dermatology] |
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The Future of Targeted Kinase Inhibitors in Melanoma | There is a future for targeted kinase inhibitors in melanoma: in new applications such as adjuvant or neoadjuvant therapy and in novel combinations with immunotherapies or other targeted therapies. [Pharmacology & Therapeutics] |
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Kezar Announces Topline Results from PRESIDIO Trial of Zetomipzomib for the Treatment of Dermatomyositis and Polymyositis
| Kezar Life Sciences, Inc. announced topline results from the PRESIDIO Phase II clinical trial of zetomipzomib in patients with dermatomyositis and polymyositis. [Kezar Life Sciences, Inc.] |
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| November 10 -12, 2022 Bordeaux, France |
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| Howard Hughes Medical Institute – New York, New York, United States |
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| University of Texas MD Anderson Cancer Center – Houston, Texas, United States |
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| City of Hope – Duarte, California, United States |
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| Fred Hutchinson Cancer Center – Seattle, Washington, United States |
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