Suppr超能文献

一种不依赖紫外线的局部小分子方法用于人类皮肤黑色素生成

A UV-Independent Topical Small-Molecule Approach for Melanin Production in Human Skin.

作者信息

Mujahid Nisma, Liang Yanke, Murakami Ryo, Choi Hwan Geun, Dobry Allison S, Wang Jinhua, Suita Yusuke, Weng Qing Yu, Allouche Jennifer, Kemeny Lajos V, Hermann Andrea L, Roider Elisabeth M, Gray Nathanael S, Fisher David E

机构信息

Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA 02118, USA; Cutaneous Biology Research Center, Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cell Rep. 2017 Jun 13;19(11):2177-2184. doi: 10.1016/j.celrep.2017.05.042.

Abstract

The presence of dark melanin (eumelanin) within human epidermis represents one of the strongest predictors of low skin cancer risk. Topical rescue of eumelanin synthesis, previously achieved in "redhaired" Mc1r-deficient mice, demonstrated significant protection against UV damage. However, application of a topical strategy for human skin pigmentation has not been achieved, largely due to the greater barrier function of human epidermis. Salt-inducible kinase (SIK) has been demonstrated to regulate MITF, the master regulator of pigment gene expression, through its effects on CRTC and CREB activity. Here, we describe the development of small-molecule SIK inhibitors that were optimized for human skin penetration, resulting in MITF upregulation and induction of melanogenesis. When topically applied, pigment production was induced in Mc1r-deficient mice and normal human skin. These findings demonstrate a realistic pathway toward UV-independent topical modulation of human skin pigmentation, potentially impacting UV protection and skin cancer risk.

摘要

人类表皮中深色黑色素(真黑素)的存在是皮肤癌风险低的最强预测指标之一。先前在“红发”的Mc1r基因缺陷小鼠中实现的真黑素合成的局部挽救,显示出对紫外线损伤的显著保护作用。然而,尚未实现针对人类皮肤色素沉着的局部策略应用,这主要是由于人类表皮具有更强的屏障功能。盐诱导激酶(SIK)已被证明可通过其对CRTC和CREB活性的影响来调节MITF,即色素基因表达的主要调节因子。在此,我们描述了针对人类皮肤渗透进行优化的小分子SIK抑制剂的开发,其导致MITF上调并诱导黑色素生成。局部应用时,在Mc1r基因缺陷小鼠和正常人类皮肤中均可诱导色素生成。这些发现证明了一条通向不依赖紫外线的人类皮肤色素沉着局部调节的现实途径,可能会影响紫外线防护和皮肤癌风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf3/5549921/5b093d0d1c3d/nihms882886f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验