MicroRNA-21 silencing enhances the cytotoxic effect of the antiangiogenic drug sunitinib in glioblastoma

• Published in: Human molecular genetics Vol. 22; no. 5; pp. 904 - 918
• Main Authors: Costa, Pedro M, Cardoso, Ana L, Nóbrega, Clévio, Pereira de Almeida, Luís F, Bruce, Jeffrey N, Canoll, Peter, Pedroso de Lima, Maria C
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.03.2013
• Subjects: Angiogenesis Inhibitors - administration & dosage; Animals; Apoptosis Regulatory Proteins - genetics; Brain Neoplasms - drug therapy; Brain Neoplasms - genetics; Brain Neoplasms - pathology; Cell Line, Tumor; Cell Proliferation; Down-Regulation; Gene Expression Regulation, Neoplastic; Glioblastoma - drug therapy; Glioblastoma - genetics; Glioblastoma - pathology; Humans; Indoles - administration & dosage; Mice; MicroRNAs - genetics; MicroRNAs - metabolism; PTEN Phosphohydrolase - genetics; Pyrroles - administration & dosage; RNA-Binding Proteins - genetics; Signal Transduction; Up-Regulation
• ISSN: 0964-6906; 1460-2083
• DOI: 10.1093/hmg/dds496

Highly malignant glioblastoma (GBM) is characterized by high genetic heterogeneity and infiltrative brain invasion patterns, and aberrant miRNA expression has been associated with hallmark malignant properties of GBM. The lack of effective GBM treatment options prompted us to investigate whether miRNAs would constitute promising therapeutic targets toward the generation of a gene therapy approach with clinical significance for this disease. Here, we show that microRNA-21 (miR-21) is upregulated and microRNA-128 (miR-128) is downregulated in mouse and human GBM samples, a finding that is corroborated by analysis of a large set of human GBM data from The Cancer Genome Atlas. Moreover, we demonstrate that oligonucleotide-mediated miR-21 silencing in U87 human GBM cells resulted in increased levels of the tumor suppressors PTEN and PDCD4, caspase 3/7 activation and decreased tumor cell proliferation. Cell exposure to pifithrin, an inhibitor of p53 transcriptional activity, reduced the caspase activity associated with decreased miR-21 expression. Finally, we demonstrate for the first time that miR-21 silencing enhances the antitumoral effect of the tyrosine kinase inhibitor sunitinib, whereas no therapeutic benefit is observed when coupling miR-21 silencing with the first-line drug temozolomide. Overall, our results provide evidence that miR-21 is uniformly overexpressed in GBM and constitutes a highly promising target for multimodal therapeutic approaches toward GBM.