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Update on the Epidemiology of Melanoma.黑色素瘤流行病学最新进展
Curr Dermatol Rep. 2013 Mar 1;2(1):24-34. doi: 10.1007/s13671-012-0035-5.
2
Identification of microRNA-mRNA functional interactions in UVB-induced senescence of human diploid fibroblasts.鉴定 UVB 诱导人二倍体成纤维细胞衰老过程中的 microRNA-mRNA 功能相互作用。
BMC Genomics. 2013 Apr 4;14:224. doi: 10.1186/1471-2164-14-224.
3
Cutaneous alpha, beta and gamma human papillomaviruses in relation to squamous cell carcinoma of the skin: a population-based study.皮肤 alpha、beta 和 gamma 型人乳头瘤病毒与皮肤鳞状细胞癌的关系:一项基于人群的研究。
Int J Cancer. 2013 Oct 1;133(7):1713-20. doi: 10.1002/ijc.28176. Epub 2013 Apr 22.
4
DNA damage as a biological sensor for environmental sunlight.作为环境阳光的生物传感器的 DNA 损伤。
Photochem Photobiol Sci. 2013 Aug;12(8):1259-72. doi: 10.1039/c3pp00004d.
5
The biomechanical properties of the skin.皮肤的生物力学特性。
Dermatol Surg. 2013 Feb;39(2):193-203. doi: 10.1111/dsu.12095. Epub 2013 Jan 25.
6
Genome-wide epigenetic regulation of miRNAs in cancer.癌症中 miRNA 的全基因组表观遗传调控。
Cancer Res. 2013 Jan 15;73(2):473-7. doi: 10.1158/0008-5472.CAN-12-3731. Epub 2013 Jan 10.
7
MicroRNA in non-melanoma skin cancer.非黑色素瘤皮肤癌中的 microRNA。
Cancer Biomark. 2012;11(6):253-7. doi: 10.3233/CBM-2012-0274.
8
Comparative microarray analysis of microRNA expression profiles in primary cutaneous malignant melanoma, cutaneous malignant melanoma metastases, and benign melanocytic nevi.原发性皮肤恶性黑色素瘤、皮肤恶性黑色素瘤转移灶和良性黑色素痣的 microRNA 表达谱的比较微阵列分析。
Cell Tissue Res. 2013 Jan;351(1):85-98. doi: 10.1007/s00441-012-1514-5. Epub 2012 Oct 31.
9
MicroRNA-target interactions: new insights from genome-wide approaches.MicroRNA 靶标相互作用:全基因组方法的新见解。
Ann N Y Acad Sci. 2012 Oct;1271(1):118-28. doi: 10.1111/j.1749-6632.2012.06745.x.
10
Control by a hair's breadth: the role of microRNAs in the skin.毫厘之间的掌控:microRNAs 在皮肤中的作用。
Cell Mol Life Sci. 2013 Apr;70(7):1149-69. doi: 10.1007/s00018-012-1117-z. Epub 2012 Sep 15.

皮肤对紫外线辐射的反应中的 microRNAs。

MicroRNAs in skin response to UV radiation.

机构信息

Department of Dermatology, University of Wisconsin, Madison, Madison, WI, USA.

出版信息

Curr Drug Targets. 2013 Sep;14(10):1128-34. doi: 10.2174/13894501113149990184.

DOI:10.2174/13894501113149990184
PMID:23834148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3985496/
Abstract

Solar ultraviolet (UV) radiation, an ubiquitous environmental carcinogen, is classified depending on the wavelength, into three regions; short-wave UVC (200-280 nm), mid-wave UVB (280-320 nm), and long-wave UVA (320- 400 nm). The human skin, constantly exposed to UV radiation, particularly the UVB and UVA components, is vulnerable to its various deleterious effects such as erythema, photoaging, immunosuppression and cancer. To counteract these and for the maintenance of genomic integrity, cells have developed several protective mechanisms including DNA repair, cell cycle arrest and apoptosis. The network of damage sensors, signal transducers, mediators, and various effector proteins is regulated through changes in gene expression. MicroRNAs (miRNAs), a group of small non-coding RNAs, act as posttranscriptional regulators through binding to complementary sequences in the 3´-untranslated region of their target genes, resulting in either translational repression or target degradation. Recent studies show that miRNAs add an additional layer of complexity to the intricately controlled cellular responses to UV radiation. This review summarizes our current knowledge of the role of miRNAs in the regulation of the human skin response upon exposure to UV radiation.

摘要

太阳紫外线(UV)辐射是一种普遍存在的环境致癌物,根据波长可分为三个区域:短波 UVC(200-280nm)、中波 UVB(280-320nm)和长波 UVA(320-400nm)。人类皮肤经常暴露在 UV 辐射下,尤其是 UVB 和 UVA 成分,容易受到各种有害影响,如红斑、光老化、免疫抑制和癌症。为了对抗这些影响并维护基因组的完整性,细胞已经开发了几种保护机制,包括 DNA 修复、细胞周期停滞和细胞凋亡。损伤传感器、信号转导器、介质和各种效应蛋白的网络通过基因表达的变化来调节。微小 RNA(miRNA)是一组小型非编码 RNA,通过与靶基因 3'非翻译区的互补序列结合,作为转录后调节剂,从而导致翻译抑制或靶降解。最近的研究表明,miRNA 为细胞对 UV 辐射的复杂控制反应增加了一个额外的复杂层。本综述总结了我们目前对 miRNA 在调节人类皮肤对 UV 辐射暴露的反应中的作用的认识。