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参芪扶正注射液通过泛素化 HIF-1α 促进骨骼肌自噬来改善癌因性疲乏。

Shenqi Fuzheng injection facilitates skeletal muscle mitophagy mediated by the ubiquitination of HIF-1α to ameliorate cancer-associated fatigue.

机构信息

Department of Oncology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

Lingnan Medical Research Center, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

出版信息

J Cell Mol Med. 2024 Jun;28(12):e18455. doi: 10.1111/jcmm.18455.

Abstract

Cancer-related fatigue (CRF) significantly impacts the quality of life of cancer patients. This study investigates the therapeutic potential of Shenqi Fuzheng injection (SFI) in managing CRF, focusing on its mechanistic action in skeletal muscle. We utilized a CRF mouse model to examine the effects of SFI on physical endurance, monitoring activity levels, swimming times and rest periods. Proteomic analysis of the gastrocnemius muscle was performed using isobaric tags and liquid chromatography-tandem mass spectrometry to map the muscle proteome changes post-SFI treatment. Mitochondrial function in skeletal muscle was assessed via ATP bioluminescence assay. Furthermore, the regulatory role of the hypoxia inducible factor 1 subunit alpha (HIF-1α) signalling pathway in mediating SFI's effects was explored through western blotting. In CRF-induced C2C12 myoblasts, we evaluated cell viability (CCK-8 assay), apoptosis (flow cytometry) and mitophagy (electron microscopy). The study also employed pulldown, luciferase and chromatin immunoprecipitation assays to elucidate the molecular mechanisms underlying SFI's action, particularly focusing on the transcriptional regulation of PINK1 through HIF-1α binding at the PINK1 promoter region. Our findings reveal that SFI enhances physical mobility, reduces fatigue symptoms and exerts protective effects on skeletal muscles by mitigating mitochondrial damage and augmenting antioxidative responses. SFI promotes cell viability and induces mitophagy while decreasing apoptosis, primarily through the modulation of HIF-1α, PINK1 and p62 proteins. These results underscore SFI's efficacy in enhancing mitochondrial autophagy, thereby offering a promising approach for ameliorating CRF. The study not only provides insight into SFI's potential therapeutic mechanisms but also establishes a foundation for further exploration of SFI interventions in CRF management.

摘要

癌症相关性乏力(CRF)显著影响癌症患者的生活质量。本研究探讨了参芪扶正注射液(SFI)在管理 CRF 方面的治疗潜力,重点研究其在骨骼肌中的作用机制。我们使用 CRF 小鼠模型来检测 SFI 对身体耐力的影响,监测活动水平、游泳时间和休息时间。使用等压标签和液相色谱-串联质谱法对腓肠肌进行蛋白质组分析,以绘制 SFI 治疗后肌肉蛋白质组变化图谱。通过 ATP 生物发光测定法评估骨骼肌中的线粒体功能。此外,通过 Western blot 探索缺氧诱导因子 1 亚单位 alpha(HIF-1α)信号通路在介导 SFI 作用中的调节作用。在 CRF 诱导的 C2C12 成肌细胞中,我们评估了细胞活力(CCK-8 测定法)、细胞凋亡(流式细胞术)和线粒体自噬(电子显微镜)。该研究还采用下拉、荧光素酶和染色质免疫沉淀测定法阐明了 SFI 作用的分子机制,特别是通过 HIF-1α 在 PINK1 启动子区域的结合对 PINK1 的转录调节。我们的研究结果表明,SFI 通过减轻线粒体损伤和增强抗氧化反应来提高身体活动能力、减轻疲劳症状并对骨骼肌发挥保护作用。SFI 通过调节 HIF-1α、PINK1 和 p62 蛋白来促进细胞活力和诱导线粒体自噬,同时减少细胞凋亡。这些结果突出了 SFI 在增强线粒体自噬方面的疗效,为改善 CRF 提供了一种有前途的方法。该研究不仅提供了 SFI 潜在治疗机制的见解,还为进一步探索 SFI 在 CRF 管理中的干预措施奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a84/11187406/193d502e2d79/JCMM-28-e18455-g006.jpg

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