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Inhibition of DYRK1A destabilizes EGFR and reduces EGFR-dependent glioblastoma growth
Natividad Pozo, … , Juan M. Sepúlveda, Pilar Sánchez-Gómez
Natividad Pozo, … , Juan M. Sepúlveda, Pilar Sánchez-Gómez
Published May 1, 2013
Citation Information: J Clin Invest. 2013;123(6):2475-2487. https://doi.org/10.1172/JCI63623.
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Research Article Oncology

Inhibition of DYRK1A destabilizes EGFR and reduces EGFR-dependent glioblastoma growth

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Abstract

Glioblastomas (GBMs) are very aggressive tumors that are resistant to conventional chemo- and radiotherapy. New molecular therapeutic strategies are required to effectively eliminate the subpopulation of GBM tumor–initiating cells that are responsible for relapse. Since EGFR is altered in 50% of GBMs, it represents one of the most promising targets; however, EGFR kinase inhibitors have produced poor results in clinical assays, with no clear explanation for the observed resistance. We uncovered a fundamental role for the dual-specificity tyrosine phosphorylation–regulated kinase, DYRK1A, in regulating EGFR in GBMs. We found that DYRK1A was highly expressed in these tumors and that its expression was correlated with that of EGFR. Moreover, DYRK1A inhibition promoted EGFR degradation in primary GBM cell lines and neural progenitor cells, sharply reducing the self-renewal capacity of normal and tumorigenic cells. Most importantly, our data suggest that a subset of GBMs depends on high surface EGFR levels, as DYRK1A inhibition compromised their survival and produced a profound decrease in tumor burden. We propose that the recovery of EGFR stability is a key oncogenic event in a large proportion of gliomas and that pharmacological inhibition of DYRK1A could represent a promising therapeutic intervention for EGFR-dependent GBMs.

Authors

Natividad Pozo, Cristina Zahonero, Paloma Fernández, Jose M. Liñares, Angel Ayuso, Masatoshi Hagiwara, Angel Pérez, Jose R. Ricoy, Aurelio Hernández-Laín, Juan M. Sepúlveda, Pilar Sánchez-Gómez

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Figure 1

DYRK1A interference affects the levels of EGFR and the tumorigenic capacity of established GBM cell lines.

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DYRK1A interference affects the levels of EGFR and the tumorigenic capac...
(A) GBM cell lines were infected with the shControl or shDYRK1A lentivirus, and the capacity to form secondary spheres was measured. Bottom Western blot panels illustrate the inhibition of kinase expression. (B) Flow cytometric analysis of the percentage of EGFR-positive cells after lentiviral infection of 2 GBM cell lines. Bottom Western blot panels display the amount of total EGFR protein. (C) Images show representative vimentin staining of tumors formed after implantation of 10,000 puromycin-selected shControl- or shDYRK1A-infected U87 cells. Graphs on the right show the quantification of tumor volume. (D) Number of EGFR-positive cells per tumorigenic field, with representative images shown on the right. (E) Puromycin-selected shControl- or shDYRK1A-infected U87 cells (3 × 106) were implanted into the flanks of nude mice. Tumor size was measured once every 4–5 days. Relative tumor volume = tumor volume measured/tumor volume at day 25. (F) Proportion of BrdU-positive cells in shControl and shDYRK1A tumor tissues. (G) Number of activated caspase 3–positive (Act. casp3-positive) cells in the tumor tissues. Scale bars: 800 μm (C); 50 μm (D). *P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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