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The long-lasting protective effect of HGF in cardiomyoblasts exposed to doxorubicin requires a positive feed-forward loop mediated by ERK1,2-TIMP1-STAT3

Title: The long-lasting protective effect of HGF in cardiomyoblasts exposed to doxorubicin requires a positive feed-forward loop mediated by ERK1,2-TIMP1-STAT3
Authors: Gallo S.; Spilinga M.; Casanova E.; Bonzano A.; Boccaccio C.; Comoglio P. M.; Crepaldi T.
Contributors: Gallo S.; Spilinga M.; Casanova E.; Bonzano A.; Boccaccio C.; Comoglio P.M.; Crepaldi T.
Publication Year: 2020
Collection: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
Subject Terms: Anthracycline; Apoptosi; Cardiac injury; DNA damage; Erk1,2; HGF; Met receptor; Stat3; Timp1
Description: Previous studies showed that the hepatocyte growth factor (HGF)–Met receptor axis plays long-lasting cardioprotection against doxorubicin anti-cancer therapy. Here, we explored the mechanism(s) underlying the HGF protective effect. DNA damage was monitored by histone H2AX phosphorylation and apoptosis by proteolytic cleavage of caspase 3. In doxorubicin-treated H9c2 cardiomyoblasts, the long-lasting cardioprotection is mediated by activation of the Ras/Raf/Mek/Erk (extracellular signal-regulated kinase 1,2) signaling pathway and requires Stat3 (signal transducer and activator of transcription 3) activation. The HGF protection was abrogated by the Erk1,2 inhibitor, PD98059. This translated into reduced Y705 phosphorylation and impaired nuclear translocation of Stat3, showing crosstalk between Erk1,2 and Stat3 signaling. An array of 29 cytokines, known to activate Stat3, was interrogated to identify the molecule(s) linking the two pathways. The analysis showed a selective increase in expression of the tissue inhibitor of metalloproteinases-1 (Timp1). Consistently, inhibition in cardiomyoblasts of Timp1 translation by siRNAs blunted both Stat3 activation and the cardioprotective effect of HGF. Thus, Timp1 is responsible for the generation of a feed-forward loop of Stat3 activation and helps cardiomyocytes to survive during the genotoxic stress induced by anthracyclines.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/32722178; info:eu-repo/semantics/altIdentifier/wos/WOS:000559068200001; volume:21; issue:15; firstpage:1; lastpage:15; numberofpages:15; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/2318/1770093; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85088812328
DOI: 10.3390/ijms21155258
Availability: https://hdl.handle.net/2318/1770093; https://doi.org/10.3390/ijms21155258
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.6F487AC9
Database: BASE