Department of Neurosurgery, Shandong Cancer Hospital, Shandong Academy of Medical Sciences, Jinan 250117, PR China.
Oncol Rep. 2012 Apr;27(4):1200-6. doi: 10.3892/or.2011.1588. Epub 2011 Dec 12.
MicroRNAs (miRNAs) are endogenously small non-coding RNAs which are key post-transcriptional regulators of gene expression. Deregulation of miRNAs is common in human tumorigenesis. We report that miRNA-205 is significantly down-regulated in glioma cell lines and tissue specimens. Ectopic expression of miRNA-205 induces apoptosis, cell cycle arrest, impairs cell viability, clonability and invasive properties of glioma cells. We further demonstrate that miRNA-205 can specifically suppress expression of VEGF-A by directly interacting with the putative miRNA-205 binding site at the 3'-UTR. Identification of VEGF-A as a direct target for miRNA-205 may imply that miRNA-205 is a novel target for glioma therapy. Taken together, the present study for the first time provides evidence that miRNA-205 is a glioma-specific tumor suppressor by targeting VEGF-A.
MicroRNAs (miRNAs) 是内源性的小非编码 RNA,是基因表达的关键转录后调控因子。miRNAs 的失调在人类肿瘤发生中很常见。我们报告说,miRNA-205 在神经胶质瘤细胞系和组织标本中显著下调。miRNA-205 的异位表达诱导神经胶质瘤细胞凋亡、细胞周期停滞、损害细胞活力、克隆形成能力和侵袭特性。我们进一步证明,miRNA-205 可以通过直接与 3'UTR 上的假定 miRNA-205 结合位点相互作用,特异性抑制 VEGF-A 的表达。鉴定 VEGF-A 为 miRNA-205 的直接靶标可能意味着 miRNA-205 是神经胶质瘤治疗的新靶标。总之,本研究首次提供证据表明,miRNA-205 通过靶向 VEGF-A 是一种神经胶质瘤特异性肿瘤抑制因子。