A Sox2:miR-486-5p axis regulates survival of GBM cells by inhibiting tumor suppressor networks

Hernando Lopez-Bertoni, Ivan S. Kotchetkov, Nicole Mihelson, Bachchu Lal, Yuan Rui, Heather Ames, Maria Lugo-Fagundo, Hugo Guerrero-Cazares, Alfredo Quinones-Hinojosa, Jordan J. Green, John Laterra

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


Glioblastoma multiforme (GBM) and other solid malignancies are heterogeneous and contain subpopulations of tumor cells that exhibit stem-like features. Our recent findings point to a dedifferentiation mechanism by which reprogramming transcription factors Oct4 and Sox2 drive the stem-like phenotype in glioblastoma, in part, by differentially regulating subsets of miRNAs. Currently, the molecular mechanisms by which reprogramming transcription factors and miRNAs coordinate cancer stem cell tumorpropagating capacity are unclear. In this study, we identified miR-486-5p as a Sox2-induced miRNA that targets the tumor suppressor genes PTEN and FoxO1 and regulates the GBM stem-like cells. miR-486-5p associated with the GBM stem cell phenotype and Sox2 expression and was directly induced by Sox2 in glioma cell lines and patient-derived neurospheres. Forced expression of miR-486-5p enhanced the self-renewal capacity of GBM neurospheres, and inhibition of endogenous miR-486-5p activated PTEN and FoxO1 and induced cell death by upregulating proapoptotic protein BIM via a PTEN-dependent mechanism. Furthermore, delivery of miR-486-5p antagomirs to preestablished orthotopic GBM neurosphere-derived xenografts using advanced nanoparticle formulations reduced tumor sizes in vivo and enhanced the cytotoxic response to ionizing radiation. These results define a previously unrecognized and therapeutically targetable Sox2:miR-486-5p axis that enhances the survival of GBM stem cells by repressing tumor suppressor pathways. Significance: This study identifies a novel axis that links core transcriptional drivers of cancer cell stemness to miR-486-5p- dependent modulation of tumor suppressor genes that feeds back to regulate glioma stem cell survival.

Original languageEnglish (US)
Pages (from-to)1644-1655
Number of pages12
JournalCancer research
Issue number8
StatePublished - Apr 15 2020

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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