Candiolo Cancer Institute, FPO-IRCCS, SP142, Km3.95, 10060 Candiolo, TO, Italy.
Department of Oncology, University of Turin, Regione Gonzole 10, 10043 Orbassano, TO, Italy.
Int J Mol Sci. 2020 Jul 24;21(15):5258. doi: 10.3390/ijms21155258.
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.
先前的研究表明,肝细胞生长因子(HGF)-Met 受体轴对阿霉素抗癌治疗具有持久的心脏保护作用。在这里,我们探讨了 HGF 保护作用的机制。通过组蛋白 H2AX 磷酸化监测 DNA 损伤,通过半胱天冬酶 3 的蛋白水解裂解监测细胞凋亡。在阿霉素处理的 H9c2 心肌细胞中,这种持久的心脏保护作用是通过 Ras/Raf/Mek/Erk(细胞外信号调节激酶 1、2)信号通路的激活介导的,并且需要 Stat3(信号转导和转录激活因子 3)的激活。Erk1、2 抑制剂 PD98059 可阻断 HGF 的保护作用。这导致 Y705 磷酸化减少和 Stat3 核易位受损,表明 Erk1、2 和 Stat3 信号之间存在串扰。我们检测了一组已知可激活 Stat3 的 29 种细胞因子,以鉴定连接两条通路的分子。分析显示组织金属蛋白酶抑制剂-1(Timp1)的表达选择性增加。一致地,用 siRNAs 抑制心肌细胞中 Timp1 的翻译,既削弱了 Stat3 的激活,也削弱了 HGF 的心脏保护作用。因此,Timp1 负责 Stat3 激活的正反馈环的产生,并有助于心肌细胞在蒽环类药物诱导的遗传毒性应激下存活。