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Dysfunctional EGFR and oxidative stress-induced PKD1 signaling drive formation of DCLK1+ pancreatic stem cells.

ABSTRACT: Doublecortin-like kinase 1 (DCLK1)-positive pancreatic cancer stem cells develop at a precancerous stage and may contribute to the lack of efficacy of pancreatic cancer therapy. Although PanIN cells express oncogenic KRas and have an increased activity of epidermal growth factor receptor (EGFR), we demonstrate that, in DCLK1⁺ PanIN cells, EGFR signaling is not propagated to the nucleus. Mimicking blockage of EGFR with erlotinib in PanIN organoid culture or in p48^cre;Kras^G12D mice led to a significant increase in DCLK1⁺ PanIN cells. As a mechanism of how EGFR inhibition leads to formation of DCLK1⁺ cells, we identify an increase in hydrogen peroxide contributing to activation of Protein Kinase D1 (PKD1). Active PKD1 then drives stemness and abundance of DCLK1⁺ cells in lesions. Our data suggest a signaling mechanism that leads to the development of DCLK1⁺ pancreatic cancer stem cells, which can be exploited to target this population in potential therapeutic approaches.

SUBMITTER: Fleming Martinez AK

PROVIDER: S-EPMC7820128 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Mutant KRas-Induced Mitochondrial Oxidative Stress in Acinar Cells Upregulates EGFR Signaling to Drive Formation of Pancreatic Precancerous Lesions.

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DCLK1 marks a morphologically distinct subpopulation of cells with stem cell properties in preinvasive pancreatic cancer.

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2016-04-11 | GSE74429 | GEO

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