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Theranostics 2019; 9(17):4860-4877. doi:10.7150/thno.35882 This issue Cite

Research Paper

HIF-1α/Wnt signaling-dependent control of gene transcription regulates neuronal differentiation of glioblastoma stem cells

Daniele Boso¹, Elena Rampazzo^1✉, Carlo Zanon², Silvia Bresolin¹, Francesca Maule¹, Elena Porcù¹, Alice Cani¹, Alessandro Della Puppa³, Luca Trentin¹, Giuseppe Basso^1,2, Luca Persano^1,2✉

1. Department of Woman and Children's Health, University of Padova, Padova, Italy.
2. Istituto di Ricerca Pediatrica - Città della Speranza - IRP, Padova, Italy.
3. Neurosurgery Unit, Padova University Hospital, Padova, Italy.

✉ Corresponding authors: Dr. Elena Rampazzo, PhD, Department of Woman and Children's Health, University of Padova, 35128, Padova, ITALY; Ph: +39 049 821 5485; e-mail: elena.rampazzoit or alternatively: Dr. Luca Persano, PhD, Department of Woman and Children's Health, University of Padova, 35128, Padova, ITALY; Ph: +39 049 821 5487; e-mail: luca.persanoit More

Abstract

HIF-1α has been suggested to interplay with Wnt signaling components in order to activate a neuronal differentiation process in both normal brain and glioblastoma (GBM). Based on these data, we explored the molecular mechanisms underlying the observed capability of GBM cells to acquire a neuronal phenotype upon Wnt signaling stimulation and how the microenvironment, particularly hypoxia, modulates this process.

Methods: here, the employment of ChIP-seq techniques together with co-immunoprecipitation approaches allowed to reconstruct the molecular interactions responsible for activating specific pro-differentiating transcriptional programs in GBM cells. Moreover, gene silencing/over-expression approaches coupled with the functional analysis of cell phenotype were applied to confirm ChIP-driven hypotheses. Finally, we combined the use of publicly available gene expression datasets with protein expression data by immunohistochemistry to test the clinical relevance of obtained results.

Results: our data clearly suggest that HIF-1α is recruited by the β-catenin/TCF1 complex to foster neuronal differentiation gene transcription in hypoxic GBM cells. Conversely, at higher oxygen levels, the increased expression of TCF4 exerts a transcriptional inhibitory function on the same genomic regions, thus counteracting differentiation. Moreover, we demonstrate the existence of a positive correlation between the expression levels of HIF-1α, TCF1 and neuronal phenotype in GBM tumors, accompanied by the over-expression of several Wnt signaling components, finally affecting patient prognosis.

Conclusion: we unveiled a peculiar mechanism by which TCF1 and HIF-1α can induce a reminiscent neuronal differentiation of hypoxic GBM cells, which is hampered, in normoxia, by high levels of TCF4, thus not only de facto controlling the balance between differentiation and stemness, but also impacting on intra-tumoral heterogeneity and eventually patient outcome.

Keywords: Cancer stem cells, glioblastoma, HIF-1α, neuronal differentiation.

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