Investigating miRNA-mRNA regulatory networks using crosslinking immunoprecipitation methods for biomarker and target discovery in cancer

被引:8
|
作者
Prado, Mireia Mato [1 ]
Frampton, Adam E. [1 ,2 ]
Giovannetti, Elisa [3 ,4 ,5 ]
Stebbing, Justin [1 ]
Castellano, Leandro [1 ]
Krell, Jonathan [1 ]
机构
[1] Imperial Coll, Imperial Ctr Translat & Expt Med, Dept Surg & Canc, Div Canc, Hammersmith Hosp Campus,Du Cane Rd, London W12 0NN, England
[2] Imperial Coll, Dept Surg & Canc, HPB Surg Unit, London, England
[3] Vrije Univ Amsterdam, Dept Med Oncol, Med Ctr, Amsterdam, Netherlands
[4] Univ Pisa, Canc Pharmacol Lab, AIRC Start Up Unit, Pisa, Italy
[5] CNR Nano, Inst Nanosci & Nanotechnol, Pisa, Italy
关键词
microRNA; cancer; targetome; therapy; PAR-CLIP; biomarker; CLASH; RNA sequencing; pancreatic Cancer; WEB SERVER; MICRORNA BIOGENESIS; BINDING PROTEIN; NUCLEAR EXPORT; ARGONAUTE CLIP; PREDICTION; IDENTIFICATION; REVEALS; SITES; COMPLEX;
D O I
10.1080/14737159.2016.1239532
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level. Recently, different experimental approaches, such as RNA Sequencing, crosslinking immunoprecipitation (CLIP) methods and its variations, together with computational approaches have been developed to elucidate the miRNA-mRNA targetome.Areas covered: This report focuses on comparing the different experimental and computational approaches, describing their advantages and disadvantages and providing several examples of preclinical (in vitro and in vivo) and clinical studies that have identified miRNA target genes in various tumour types, including breast, ovary, colorectal and pancreas.Expert commentary: The combination of CLIP methods with bioinformatic analyses is essential to better predict miRNA-mRNA interactions and associate their specific pathways within the extensive regulatory network. Nevertheless, further studies are needed to overcome the difficulties these methods have, in order to find a gold standard method that identifies, without any bias, the regulatory association between miRNAs and their target mRNAs.
引用
收藏
页码:1155 / 1162
页数:8
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