Literature DB >> 17465885

miRNA: licensed to kill the messenger.

Chandan K Sen, Sashwati Roy.   

Abstract

Current developments have brought non-coding genes under limelight together with their better-known siblings, the coding genes or mRNA. The 2006 Nobel Prize in Physiology or Medicine was awarded to Andrew Fire and Craig Mello for their 1998 discovery that double-stranded RNA triggers suppression of gene activity in a homology-dependent manner, a process named RNA interference (RNAi). Post-transcriptional regulation of genes was generally regarded as an odd regulatory mechanism for several years until it was learnt that regulatory trans-acting antisense RNAs exist in several species. Identification of a large number of small RNA molecules called microRNAs (miRNAs) elevated the overall field of biomedical RNAi to the striking level of current recognition. miRNAs represent a class of endogenous small ( approximately 22 nucleotides) RNA molecules that can repress protein synthesis. It is estimated that there are over 600 miRNAs in mammalian cells, and that about 30% of all genes are regulated by miRNA. Current understanding of the molecular mechanism of any disease would be incomplete without factoring in the functional significance of miRNA. In the category of the futuristic RNAi drugs, miRNA-based therapies are promising. The field has progressed rapidly as it relates to cancer research (highlighted in DNA and Cell Biology Volume 26, Number 4), while development in most other areas (highlighted in DNA and Cell Biology Volume 26, Number 3) of biomedical research remains in its infancy, offering significant opportunity for researchers. Approaches to interfere with miRNA function in vivo offer novel therapeutic opportunities. Lessons in gene therapy have taught us that tinkering with the genetic machinery comes with its own set of risks, especially in a clinical setting. miRNA-based therapies are also subject to such risks, which need to be prudently managed. Having acknowledged the potential risk, we have to recognize that new knowledge about the functional roles of miRNA is revolutionizing cell biology and will have a major impact on biomedical research imminently.

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Year:  2007        PMID: 17465885     DOI: 10.1089/dna.2006.0567

Source DB:  PubMed          Journal:  DNA Cell Biol        ISSN: 1044-5498            Impact factor:   3.311


  14 in total

1.  Conserved long noncoding RNAs transcriptionally regulated by Oct4 and Nanog modulate pluripotency in mouse embryonic stem cells.

Authors:  Jameelah Sheik Mohamed; Philip Michael Gaughwin; Bing Lim; Paul Robson; Leonard Lipovich
Journal:  RNA       Date:  2009-12-21       Impact factor: 4.942

Review 2.  miRNA in Macrophage Development and Function.

Authors:  Sashwati Roy
Journal:  Antioxid Redox Signal       Date:  2016-08-19       Impact factor: 8.401

Review 3.  MiRNA in innate immune responses: novel players in wound inflammation.

Authors:  Sashwati Roy; Chandan K Sen
Journal:  Physiol Genomics       Date:  2010-12-07       Impact factor: 3.107

Review 4.  Identifying targets for preventing epilepsy using systems biology.

Authors:  Jeffrey A Loeb
Journal:  Neurosci Lett       Date:  2011-03-04       Impact factor: 3.046

Review 5.  miR-210: the master hypoxamir.

Authors:  Yuk C Chan; Jaideep Banerjee; Sang Yong Choi; Chandan K Sen
Journal:  Microcirculation       Date:  2012-04       Impact factor: 2.628

Review 6.  microRNA-200b as a Switch for Inducible Adult Angiogenesis.

Authors:  Mithun Sinha; Subhadip Ghatak; Sashwati Roy; Chandan K Sen
Journal:  Antioxid Redox Signal       Date:  2015-05-10       Impact factor: 8.401

Review 7.  MicroRNA signature and regulatory functions in the endometrium during normal and disease states.

Authors:  Qun Pan; Nasser Chegini
Journal:  Semin Reprod Med       Date:  2008-10-24       Impact factor: 1.303

8.  High throughput genome-wide survey of small RNAs from the parasitic protists Giardia intestinalis and Trichomonas vaginalis.

Authors:  Xiaowei Sylvia Chen; Lesley J Collins; Patrick J Biggs; David Penny
Journal:  Genome Biol Evol       Date:  2009-07-06       Impact factor: 3.416

9.  MicroRNA-21 promotes hepatocellular carcinoma HepG2 cell proliferation through repression of mitogen-activated protein kinase-kinase 3.

Authors:  Guangxian Xu; Yilin Zhang; Jun Wei; Wei Jia; Zhaohui Ge; Zhaobo Zhang; Xiaoming Liu
Journal:  BMC Cancer       Date:  2013-10-10       Impact factor: 4.430

10.  Base Composition Characteristics of Mammalian miRNAs.

Authors:  Bin Wang
Journal:  J Nucleic Acids       Date:  2013-02-24
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