Department of Biotechnology, University of Natural Resources and Applied Life Sciences Vienna, Austria.
Biogerontology. 2010 Aug;11(4):501-6. doi: 10.1007/s10522-010-9272-9. Epub 2010 May 1.
The miR-17-92 cluster encoding 6 single mature miRNAs was identified a couple of years ago to contain the first oncogenic miRNAs. Now, one of these 6 miRNAs, miR-19 has been identified as the key responsible for this oncogenic activity. This in turn reduces PTEN levels and in consequence activates the AKT/mTOR pathway that is also prominently involved in modulation of organismal life spans. In contrast, miR-19 and other members of the miR-17-92 cluster are found to be commonly downregulated in several human replicative and organismal aging models. Taken together, these findings suggest that miR-19 and the other members of the miR-17-92 cluster might be important regulators on the cross-roads between aging and cancer. Therefore, we here briefly summarize how this cluster is transcriptionally regulated, which target mRNAs have been confirmed so far and how this might be linked to modulation of organismal life-spans.
几年前,人们发现 miR-17-92 簇编码的 6 个单成熟 miRNA 是第一个致癌 miRNA。现在,这 6 个 miRNA 中的一个,miR-19,被确定为这种致癌活性的关键因素。这反过来又降低了 PTEN 的水平,并激活了 AKT/mTOR 途径,该途径也显著参与调节生物体的寿命。相比之下,miR-19 和 miR-17-92 簇的其他成员在几种人类复制和生物体衰老模型中被发现普遍下调。综上所述,这些发现表明,miR-19 和 miR-17-92 簇的其他成员可能是衰老和癌症之间的交叉点的重要调节因子。因此,我们在这里简要总结了这个簇是如何转录调控的,迄今为止已经确认了哪些靶 mRNA,以及这如何与调节生物体的寿命相关。