MicroRNA dysregulation in melanoma

被引:52
作者
Latchana, Nicholas [1 ]
Ganju, Akaansha [1 ]
Howard, J. Harrison [1 ]
Carson, William E., III [1 ,2 ,3 ]
机构
[1] Ohio State Univ, Dept Surg, Columbus, OH 43210 USA
[2] Ohio State Univ, Arthur G James Comprehens Canc Ctr, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[3] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43210 USA
来源
SURGICAL ONCOLOGY-OXFORD | 2016年 / 25卷 / 03期
关键词
Melanoma; MicroRNA; DIFFERENTIAL EXPRESSION; MALIGNANT-MELANOMA; CANCER-THERAPY; MIR-211; SIGNATURE; MIR-125B; DIAGNOSIS; DELIVERY; INVASION; MIRNAS;
D O I
10.1016/j.suronc.2016.05.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Melanoma is the deadliest form of skin cancer. Current challenges facing the management of melanoma include accurate prediction of individuals who will respond to adjuvant therapies as well as early detection of recurrences. These and other challenges have prompted investigation into biomarkers that could be used as diagnostic, prognostic and therapeutic aids. MicroRNAs (miRs) are small 19-22 nucleotide RNA inhibitors of protein translation. Over 800 different miRs are present within cells and importantly miR expression profiles may vary across different cells types and stages of malignancy. Unique expression profiles have been described for malignant melanoma; however, this work has yet to be translated into routine clinical practice. We highlight pertinent studies involving common miRs implicated in the oncogenesis of melanoma including miR-21, miR-125b, miR-150, miR-155, miR-205, and miR-211. In particular, emphasis is placed upon differential expression across different stages of melanoma progression, prognostic implications and potential mechanistic involvement. Focused efforts on inhibition of these miRs could be the most efficient method of translating preclinical endeavors into clinically meaningful applications. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:184 / 189
页数:6
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