The role of microRNAs and long non-coding RNAs in the pathology, diagnosis, and management of melanoma

被引:65
|
作者
Aftab, Muhammad Nauman [1 ,4 ]
Dinger, Marcel E. [2 ,3 ]
Perera, Ranjan J. [1 ]
机构
[1] Sanford Burnham Med Res Inst, Orlando, FL 32827 USA
[2] Univ New S Wales, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[3] Univ New S Wales, St Vincents Clin Sch, Darlinghurst, NSW 2010, Australia
[4] Govt Coll Univ, Inst Ind Biotechnol, Lahore 54000, Pakistan
基金
美国国家卫生研究院;
关键词
Noncoding RNAs; MicroRNAs; Melanoma; Molecular function; CELL-CYCLE PROGRESSION; FACTOR-KAPPA-B; MALIGNANT-MELANOMA; TRANSCRIPTION FACTOR; GENE-EXPRESSION; DOWN-REGULATION; GROWTH-FACTOR; NEURAL CREST; C-MET; CIRCULATING MIRNAS;
D O I
10.1016/j.abb.2014.07.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melanoma is frequently lethal and its global incidence is steadily increasing. Despite the rapid development of different modes of targeted treatment, durable clinical responses remain elusive. A complete understanding of the molecular mechanisms that drive melanomagenesis is required, both genetic and epigenetic, in order to improve prevention, diagnosis, and treatment. There is increased appreciation of the role of microRNAs (miRNAs) in melanoma biology, including in proliferation, cell cycle, migration, invasion, and immune evasion. Data are also emerging on the role of long non-coding RNAs (IncRNAs), such as SPRY4-IT1, BANCR, and HOTAIR, in melanomagenesis. Here we review the data on the miRNAs and IncRNAs implicated in melanoma biology. An overview of these studies will be useful for providing insights into mechanisms of melanoma development and the miRNAs and IncRNAs that might be useful biomarkers or future therapeutic targets. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:60 / 70
页数:11
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