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10.1111/j.1582-4934.2008.00556.x

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suck abstract from ncbi


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pmid19175699
      J+Cell+Mol+Med 2009 ; 13 (1 ): 39-53
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  • miR-21: a small multi-faceted RNA #MMPMID19175699
  • Krichevsky AM ; Gabriely G
  • J Cell Mol Med 2009[Jan]; 13 (1 ): 39-53 PMID19175699 show ga
  • More than 1000 microRNAs (miRNAs) are expressed in human cells, some tissue or cell type specific, others considered as house-keeping molecules. Functions and direct mRNA targets for some miRNAs have been relatively well studied over the last years. Every miRNA potentially regulates the expression of numerous protein-coding genes (tens to hundreds), but it has become increasingly clear that not all miRNAs are equally important; diverse high-throughput screenings of various systems have identified a limited number of key functional miRNAs over and over again. Particular miRNAs emerge as principal regulators that control major cell functions in various physiological and pathophysiological settings. Since its identification 3 years ago as the miRNA most commonly and strongly up-regulated in human brain tumour glioblastoma [1], miR-21 has attracted the attention of researchers in various fields, such as development, oncology, stem cell biology and aging, becoming one of the most studied miRNAs, along with let-7, miR-17-92 cluster ('oncomir-1'), miR-155 and a few others. However, an miR-21 knockout mouse has not yet been generated, and the data about miR-21 functions in normal cells are still very limited. In this review, we summarise the current knowledge of miR-21 functions in human disease, with an emphasis on its regulation, oncogenic role, targets in human cancers, potential as a disease biomarker and novel therapeutic target in oncology.
  • |*MicroRNAs/genetics/metabolism [MESH]
  • |Animals [MESH]
  • |Apoptosis/physiology [MESH]
  • |Base Sequence [MESH]
  • |Biomarkers, Tumor [MESH]
  • |Cell Cycle/physiology [MESH]
  • |Disease/genetics [MESH]
  • |Gene Expression Regulation, Neoplastic [MESH]
  • |Humans [MESH]
  • |Molecular Sequence Data [MESH]
  • |Neoplasms/*genetics/pathology/*physiopathology/therapy [MESH]
  • |RNA Processing, Post-Transcriptional [MESH]


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