He Xingyue, He Lin, Hannon Gregory J
Watson School of Biological Sciences, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, NY 11724, USA.
Cancer Res. 2007 Dec 1;67(23):11099-101. doi: 10.1158/0008-5472.CAN-07-2672.
Several microRNAs (miRNAs) have been implicated in tumor development based on both changes in their expression patterns and gene structural alterations in human tumors. However, we are only now beginning to see how miRNAs interact with classic oncogene and tumor suppressor mechanisms. Several recent studies have implicated the miR-34 family of miRNAs in the p53 tumor suppressor network. The expression of miR-34a, miR-34b, and miR-34c is robustly induced by DNA damage and oncogenic stress in a p53-dependent manner. When overexpressed, miR-34 leads to apoptosis or cellular senescence, whereas reduction of miR-34 function attenuates p53-mediated cell death. These findings, together with the fact that miR-34 is down-regulated in several types of human cancer, show that miRNAs can affect tumorigenesis by working within the confines of well-known tumor suppressor pathways.
基于人类肿瘤中微小RNA(miRNA)表达模式的变化和基因结构改变,已有几种miRNA被认为与肿瘤发生有关。然而,我们直到现在才开始了解miRNA如何与经典癌基因和肿瘤抑制机制相互作用。最近的几项研究表明,miRNA的miR-34家族参与了p53肿瘤抑制网络。DNA损伤和致癌应激以p53依赖的方式强烈诱导miR-34a、miR-34b和miR-34c的表达。当miR-34过表达时,会导致细胞凋亡或细胞衰老,而miR-34功能的降低会减弱p53介导的细胞死亡。这些发现,再加上miR-34在几种人类癌症中表达下调的事实,表明miRNA可以通过在著名的肿瘤抑制途径范围内发挥作用来影响肿瘤发生。