Genome-wide analysis in PC6 electroacupuncture to ameliorate carfilzomib-induced cardiotoxicity in mice

Carfilzomib公司 心脏毒性 生物 电针 心力衰竭 转录组 Wnt信号通路 药理学 细胞凋亡 射血分数 骨骼肌 内科学 信号转导 硼替佐米 内分泌学 多发性骨髓瘤 癌症研究 微阵列分析技术 蛋白酶体抑制剂 细胞生长 信使核糖核酸 米托蒽醌 生长因子 基因表达 基因表达调控 生物信息学 下调和上调 心肌病 蛋白酶体
作者
Yuxuan Chen,Rou Peng,Yi Qian,Yizhou Lu,L Chen,Meiling Yu,Minjiao Jiang,Wei Wu,S. Lu
出处
期刊:Gene [Elsevier BV]
卷期号:897: 148090-148090 被引量:3
标识
DOI:10.1016/j.gene.2023.148090
摘要

Carfilzomib (CFZ), a proteasome inhibitor commonly used in the treatment of multiple myeloma (MM), exhibits limited clinical application due to its cardiotoxicity. In our study, electroacupuncture (EA) at Neiguan acupoint (PC6) effectively reversed CFZ-induced reduction in ejection fraction (EF) and fractional shortening (FS), demonstrating great potential effect for heart protection. Through comparative analysis of the transcriptome profile from heart samples of mice treated with DMSO control, CFZ injection, and EA stimulation, we identified a total of 770 differentially expressed genes (DEGs) in CFZ (vs. Control) group and 329 DEGs in EA (vs. CFZ) group. Specifically, CFZ (vs. Control) group exhibited 65 up-regulated DEGs and 705 down-regulated DEGs, while EA (vs. CFZ) group displayed 251 up-regulated DEGs and 78 down-regulated DEGs. Metascape analysis revealed that among these treatment groups, there were 137 co-expressed DEGs remarkably enriched in skeletal system development, cellular response to growth factor stimulus, negative regulation of Wnt signaling pathway, and muscle contraction. The expression patterns of miR-8114, Myl4, Col1a1, Tmem163, Myl7, Sln, and Fxyd3, which belong to the top 30 DEGs, were verified by quantitative real-time PCR (RT-qPCR). In summary, this study firstly discloses novel insights into the regulatory mechanisms underlying PC6-based EA therapy against CFZ-induced cardiotoxicity, potentially serving as a theoretical foundation for further clinical applications.
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