Quagliariello Vincenzo, Berretta Massimiliano, Bisceglia Irma, Giacobbe Ilaria, Iovine Martina, Giordano Vienna, Arianna Raffaele, Barbato Matteo, Izzo Francesca, Maurea Carlo, Canale Maria Laura, Paccone Andrea, Inno Alessandro, Scherillo Marino, Gabrielli Domenico, Maurea Nicola
Division of Cardiology, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, 80131 Napoli, Italy.
Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy.
Cancers (Basel). 2024 Apr 12;16(8):1487. doi: 10.3390/cancers16081487.
Anthracycline-induced cardiomyopathies and sarcopenia are frequently seen in cancer patients, affecting their overall survival and quality of life; therefore, new cardioprotective and anti-sarcopenic strategies are needed. Vericiguat is a new oral guanylate cyclase activator that reduces heart failure hospitalizations or cardiovascular death. This study highlighted the potential cardioprotective and anti-sarcopenic properties of vericiguat during anthracycline therapy. Human cardiomyocytes and primary skeletal muscle cells were exposed to doxorubicin (DOXO) with or without a pre-treatment with vericiguat. Mitochondrial cell viability, LDH, and Cytochrome C release were performed to study cytoprotective properties. Intracellular Ca content, TUNEL assay, cGMP, NLRP-3, Myd-88, and cytokine intracellular levels were quantified through colorimetric and selective ELISA methods. Vericiguat exerts significant cytoprotective and anti-apoptotic effects during exposure to doxorubicin. A drastic increase in cGMP expression and reduction in NLRP-3, MyD-88 levels were also seen in Vericiguat-DOXO groups vs. DOXO groups ( < 0.001) in both cardiomyocytes and human muscle cells. GCa vericiguat reduces cytokines and chemokines involved in heart failure and sarcopenia. The findings that emerged from this study could provide the rationale for further preclinical and clinical investigations aimed at reducing anthracycline cardiotoxicity and sarcopenia in cancer patients.
蒽环类药物引起的心肌病和肌肉减少症在癌症患者中很常见,会影响他们的总体生存率和生活质量;因此,需要新的心脏保护和抗肌肉减少症策略。维立西呱是一种新型口服鸟苷酸环化酶激活剂,可减少心力衰竭住院或心血管死亡。本研究强调了维立西呱在蒽环类药物治疗期间潜在的心脏保护和抗肌肉减少症特性。将人心肌细胞和原代骨骼肌细胞暴露于多柔比星(DOXO)中,同时或不进行维立西呱预处理。通过检测线粒体细胞活力、乳酸脱氢酶(LDH)和细胞色素C释放来研究细胞保护特性。通过比色法和选择性酶联免疫吸附测定(ELISA)方法对细胞内钙含量、TUNEL检测、环磷酸鸟苷(cGMP)、NLRP-3、髓样分化因子88(MyD-88)和细胞因子细胞内水平进行定量。维立西呱在暴露于多柔比星期间发挥显著的细胞保护和抗凋亡作用。在心肌细胞和人肌肉细胞中,维立西呱-多柔比星组与多柔比星组相比,cGMP表达显著增加,NLRP-3、MyD-88水平降低(P<0.001)。维立西呱降低了参与心力衰竭和肌肉减少症的细胞因子和趋化因子。本研究得出的结果可为进一步的临床前和临床研究提供理论依据,旨在降低癌症患者蒽环类药物的心脏毒性和肌肉减少症。