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Caloric restriction leads to druggable LSD1-dependent cancer stem cells expansion
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SYSNO ASEP 0582786 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Caloric restriction leads to druggable LSD1-dependent cancer stem cells expansion Author(s) Pallavi, R. (IT)
Gatti, E. (IT)
Durfort, T. (IT)
Stendardo, M. (IT)
Ravasio, R. (IT)
Leonardi, T. (IT)
Falvo, P. (IT)
Duso, B. A. (IT)
Punzi, S. (IT)
Xieraili, A. (IT)
Polazzi, A. (IT)
Verrelli, D. (IT)
Trastulli, D. (IT)
Ronzoni, S. (IT)
Frascolla, S. (IT)
Perticari, G. (IT)
Elgendy, Mohamed (UMG-J)
Varasi, M. (IT)
Colombo, E. (IT)
Giorgio, M. (IT)
Lanfrancone, L. (IT)
Minucci, S. (IT)
Mazzarella, L. (IT)
Pelicci, P. G. (IT)Number of authors 24 Article number 828 Source Title Nature Communications. - : Nature Publishing Group
Roč. 15, č. 1 (2024)Number of pages 18 s. Language eng - English Country US - United States Keywords growth-factor-i ; expression analysis ; gene-expression ; acute-leukemia ; apoptosis ; differentiation ; activation ; trail ; alpha ; proliferation OECD category Cell biology Method of publishing Open access Institutional support UMG-J - RVO:68378050 UT WOS 001152430000033 DOI 10.1038/s41467-023-44348-y Annotation Caloric Restriction (CR) has established anti-cancer effects, but its clinical relevance and molecular mechanism remain largely undefined. Here, we investigate CR's impact on several mouse models of Acute Myeloid Leukemias, including Acute Promyelocytic Leukemia, a subtype strongly affected by obesity. After an initial marked anti-tumor effect, lethal disease invariably re-emerges. Initially, CR leads to cell-cycle restriction, apoptosis, and inhibition of TOR and insulin/IGF1 signaling. The relapse, instead, is associated with the non-genetic selection of Leukemia Initiating Cells and the downregulation of double-stranded RNA (dsRNA) sensing and Interferon (IFN) signaling genes. The CR-induced adaptive phenotype is highly sensitive to pharmacological or genetic ablation of LSD1, a lysine demethylase regulating both stem cells and dsRNA/ IFN signaling. CR + LSD1 inhibition leads to the re-activation of dsRNA/IFN signaling, massive RNASEL-dependent apoptosis, and complete leukemia eradication in similar to 90% of mice. Importantly, CR-LSD1 interaction can be modeled in vivo and in vitro by combining LSD1 ablation with pharmacological inhibitors of insulin/IGF1 or dual PI3K/MEK blockade. Mechanistically, insulin/IGF1 inhibition sensitizes blasts to LSD1-induced death by inhibiting the anti-apoptotic factor CFLAR. CR and LSD1 inhibition also synergize in patient-derived AML and triple-negative breast cancer xenografts. Our data provide a rationale for epi-metabolic pharmacologic combinations across multiple tumors. Workplace Institute of Molecular Genetics Contact Nikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217 Year of Publishing 2025 Electronic address https://www.nature.com/articles/s41467-023-44348-y
Number of the records: 1