Pancreatic ductal adenocarcinoma (PDAC) is a lethal disease, characterized by an intense desmoplastic reaction that compresses blood vessels and limits nutrient supplies. PDAC aggressiveness largely relies on its extraordinary capability to thrive and progress in a challenging tumor microenvironment. Dysregulation of the onco-suppressor miR-15a has been extensively documented in PDAC. Here, we identified the transcription factor Fos-related antigen-2 (Fra-2) as a miR-15a target mediating the adaptive mechanism of PDAC to nutrient deprivation. We report that the IGF1 signaling pathway was enhanced in nutrient deprived PDAC cells and that Fra-2 and IGF1R were significantly overexpressed in miR-15a downmodulated PDAC patients. Mechanistically, we discovered that miR-15a repressed IGF1R expression via Fra-2 targeting. In miR-15a-low context, IGF1R hyperactivated mTOR, modulated the autophagic flux and sustained PDAC growth in nutrient deprivation. In a genetic mouse model, Mir15aKO PDAC showed Fra-2 and Igf1r upregulation and mTOR activation in response to diet restriction. Consistently, nutrient restriction improved the efficacy of IGF1R inhibition in a Fra-2 dependent manner. Overall, our results point to a crucial role of Fra-2 in the cellular stress response due to nutrient restriction typical of pancreatic cancer and support IGF1R as a promising and vulnerable target in miR-15a downmodulated PDAC.

Nutrient restriction-activated Fra-2 promotes tumor progression via IGF1R in miR-15a downmodulated pancreatic ductal adenocarcinoma / Rampioni Vinciguerra, G. L.; Capece, M.; Reggiani Bonetti, L.; Nigita, G.; Calore, F.; Rentsch, S.; Magistri, P.; Ballarin, R.; Di Benedetto, F.; Distefano, R.; Cirombella, R.; Vecchione, A.; Belletti, B.; Baldassarre, G.; Lovat, F.; Croce, C. M.. - In: SIGNAL TRANSDUCTION AND TARGETED THERAPY. - ISSN 2059-3635. - 9:1(2024), pp. N/A-N/A. [10.1038/s41392-024-01740-4]

Nutrient restriction-activated Fra-2 promotes tumor progression via IGF1R in miR-15a downmodulated pancreatic ductal adenocarcinoma

Reggiani Bonetti L.;Magistri P.;Ballarin R.;Di Benedetto F.;
2024

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a lethal disease, characterized by an intense desmoplastic reaction that compresses blood vessels and limits nutrient supplies. PDAC aggressiveness largely relies on its extraordinary capability to thrive and progress in a challenging tumor microenvironment. Dysregulation of the onco-suppressor miR-15a has been extensively documented in PDAC. Here, we identified the transcription factor Fos-related antigen-2 (Fra-2) as a miR-15a target mediating the adaptive mechanism of PDAC to nutrient deprivation. We report that the IGF1 signaling pathway was enhanced in nutrient deprived PDAC cells and that Fra-2 and IGF1R were significantly overexpressed in miR-15a downmodulated PDAC patients. Mechanistically, we discovered that miR-15a repressed IGF1R expression via Fra-2 targeting. In miR-15a-low context, IGF1R hyperactivated mTOR, modulated the autophagic flux and sustained PDAC growth in nutrient deprivation. In a genetic mouse model, Mir15aKO PDAC showed Fra-2 and Igf1r upregulation and mTOR activation in response to diet restriction. Consistently, nutrient restriction improved the efficacy of IGF1R inhibition in a Fra-2 dependent manner. Overall, our results point to a crucial role of Fra-2 in the cellular stress response due to nutrient restriction typical of pancreatic cancer and support IGF1R as a promising and vulnerable target in miR-15a downmodulated PDAC.
2024
9
1
N/A
N/A
Nutrient restriction-activated Fra-2 promotes tumor progression via IGF1R in miR-15a downmodulated pancreatic ductal adenocarcinoma / Rampioni Vinciguerra, G. L.; Capece, M.; Reggiani Bonetti, L.; Nigita, G.; Calore, F.; Rentsch, S.; Magistri, P.; Ballarin, R.; Di Benedetto, F.; Distefano, R.; Cirombella, R.; Vecchione, A.; Belletti, B.; Baldassarre, G.; Lovat, F.; Croce, C. M.. - In: SIGNAL TRANSDUCTION AND TARGETED THERAPY. - ISSN 2059-3635. - 9:1(2024), pp. N/A-N/A. [10.1038/s41392-024-01740-4]
Rampioni Vinciguerra, G. L.; Capece, M.; Reggiani Bonetti, L.; Nigita, G.; Calore, F.; Rentsch, S.; Magistri, P.; Ballarin, R.; Di Benedetto, F.; Dist...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1365723
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