| Literature DB >> 20665731 |
Maria Angelica Cortez1, Milena Sabrina Nicoloso, Masayoshi Shimizu, Simona Rossi, Gopal Gopisetty, Jennifer R Molina, Carlos Carlotti, Daniela Tirapelli, Luciano Neder, Maria Sol Brassesco, Carlos Alberto Scrideli, Luiz Gonzaga Tone, Maria-Magdalena Georgescu, Wei Zhang, Vinay Puduvalli, George Adrian Calin.
Abstract
Glioblastoma is the most frequent and malignant brain tumor, characterized by an elevated capacity for cellular proliferation and invasion. Recently, it was demonstrated that podoplanin membrane sialo-glycoprotein encoded by PDPN gene is over-expressed and related to cellular invasion in astrocytic tumors; however the mechanisms of regulation are still unknown. MicroRNAs are noncoding RNAs that regulate gene expression and several biological processes and diseases, including cancer. Nevertheless, their roles in invasion, proliferation, and apoptosis of glioblastoma are not completely understood. In this study, we focused on miR-29b and miR-125a, which were predicted to regulate PDPN, and demonstrated that these microRNAs directly target the 3' untranslated region of PDPN and inhibit invasion, apoptosis, and proliferation of glioblastomas. Furthermore, we report that miR-29b and miR-125a are downregulated in glioblastomas and also in CD133-positive cells. Taken together, these results suggest that miR-29b and miR-125a represent potential therapeutic targets in glioblastoma.Entities:
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Year: 2010 PMID: 20665731 PMCID: PMC5559292 DOI: 10.1002/gcc.20808
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006