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自噬加剧癌症恶病质中的肌肉消耗,并损害线粒体功能。

Autophagy Exacerbates Muscle Wasting in Cancer Cachexia and Impairs Mitochondrial Function.

机构信息

Department of Clinical and Biological Sciences, University of Torino, Torino, Italy.

Department of Clinical and Biological Sciences, University of Torino, Torino, Italy.

出版信息

J Mol Biol. 2019 Jul 12;431(15):2674-2686. doi: 10.1016/j.jmb.2019.05.032. Epub 2019 May 28.

Abstract

Cancer cachexia is a multifactorial syndrome characterized by anorexia, weight loss and muscle wasting that impairs patients' quality of life and survival. Aim of this work was to evaluate the impact of either autophagy inhibition (knocking down beclin-1) or promotion (overexpressing TP53INP2/DOR) on cancer-induced muscle wasting. In C26 tumor-bearing mice, stress-induced autophagy inhibition was unable to rescue the loss of muscle mass and worsened muscle morphology. Treating C26-bearing mice with formoterol, a selective β2-agonist, muscle sparing was paralleled by reduced static autophagy markers, although the flux was maintained. Conversely, the stimulation of muscle autophagy exacerbated muscle atrophy in tumor-bearing mice. TP53INP2 further promoted atrogene expression and suppressed mitochondrial dynamics-related genes. Excessive autophagy might impair mitochondrial function through mitophagy. Consistently, tumor-induced mitochondrial dysfunction was detected by reduced ex vivo muscle fiber respiration. Overall, the results evoke a central role for muscle autophagy in cancer-induced muscle wasting.

摘要

癌症恶病质是一种多因素综合征,其特征为厌食、体重减轻和肌肉消耗,从而损害患者的生活质量和生存。本研究旨在评估自噬抑制(敲低 beclin-1)或促进(过表达 TP53INP2/DOR)对癌症引起的肌肉消耗的影响。在 C26 荷瘤小鼠中,应激诱导的自噬抑制不能挽救肌肉质量的损失,反而使肌肉形态恶化。用选择性β2-激动剂福莫特罗治疗 C26 荷瘤小鼠可保留肌肉,同时减少静态自噬标志物,但通量保持不变。相反,在荷瘤小鼠中刺激肌肉自噬会加剧肌肉萎缩。TP53INP2 进一步促进了萎缩基因的表达,并抑制了与线粒体动力学相关的基因。过度的自噬可能通过自噬作用损害线粒体功能。一致地,通过体外肌肉纤维呼吸检测到肿瘤诱导的线粒体功能障碍。总的来说,这些结果提示肌肉自噬在癌症引起的肌肉消耗中起着核心作用。

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