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Cancer cachexia: an overview of diagnostic criteria and therapeutic approaches for the accredited practicing dietitian.癌症恶病质:经认证的执业营养师的诊断标准和治疗方法概述。
J Hum Nutr Diet. 2021 Feb;34(1):243-254. doi: 10.1111/jhn.12811. Epub 2020 Oct 10.
2
Exosomes of oral squamous cell carcinoma cells containing miR-181a-3p induce muscle cell atrophy and apoptosis by transmissible endoplasmic reticulum stress signaling.口腔鳞状细胞癌细胞来源的外泌体通过可传递内质网应激信号诱导肌细胞萎缩和凋亡。
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MicroRNA-mRNA Co-sequencing Identifies Transcriptional and Post-transcriptional Regulatory Networks Underlying Muscle Wasting in Cancer Cachexia.微小RNA-信使核糖核酸共测序鉴定癌症恶病质中肌肉消耗潜在的转录和转录后调控网络。
Front Genet. 2020 May 29;11:541. doi: 10.3389/fgene.2020.00541. eCollection 2020.
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MicroRNA profiling of serum exosomes in patients with osteosarcoma by high-throughput sequencing.高通量测序分析骨肉瘤患者血清外泌体中的 microRNA 谱。
J Investig Med. 2020 Apr;68(4):893-901. doi: 10.1136/jim-2019-001196. Epub 2020 Feb 13.
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miRNAs as Biomarkers in Disease: Latest Findings Regarding Their Role in Diagnosis and Prognosis.miRNAs 作为疾病的生物标志物:关于其在诊断和预后中作用的最新发现。
Cells. 2020 Jan 23;9(2):276. doi: 10.3390/cells9020276.
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Identification of microRNAs in skeletal muscle associated with lung cancer cachexia.鉴定与肺癌恶病质相关的骨骼肌中的 microRNAs。
J Cachexia Sarcopenia Muscle. 2020 Apr;11(2):452-463. doi: 10.1002/jcsm.12512. Epub 2019 Dec 11.
7
MicroRNA expression profiling analysis in serum for nasopharyngeal carcinoma diagnosis.血清中微小 RNA 表达谱分析在鼻咽癌诊断中的应用。
Gene. 2020 Feb 15;727:144243. doi: 10.1016/j.gene.2019.144243. Epub 2019 Nov 16.
8
A panel of miRNAs derived from plasma extracellular vesicles as novel diagnostic biomarkers of lung adenocarcinoma.一组来源于血浆细胞外囊泡的微小 RNA 作为肺腺癌新型诊断生物标志物。
FEBS Open Bio. 2019 Dec;9(12):2149-2158. doi: 10.1002/2211-5463.12753. Epub 2019 Nov 21.
9
HuR counteracts miR-330 to promote STAT3 translation during inflammation-induced muscle wasting.HuR 拮抗 miR-330 促进炎症诱导的肌肉减少症中的 STAT3 翻译。
Proc Natl Acad Sci U S A. 2019 Aug 27;116(35):17261-17270. doi: 10.1073/pnas.1905172116. Epub 2019 Aug 12.
10
Circulating miR-203 derived from metastatic tissues promotes myopenia in colorectal cancer patients.循环 miR-203 来源于转移组织促进结直肠癌患者的肌肉减少症。
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非编码RNA调节癌症恶病质中肌肉消耗的机制。

The mechanism by which noncoding RNAs regulate muscle wasting in cancer cachexia.

作者信息

Zhou Xueer, Hu Shoushan, Zhang Yunan, Du Guannan, Li Yi

机构信息

State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Dept. of Head and Neck Oncology, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.

出版信息

Precis Clin Med. 2021 Apr 23;4(2):136-147. doi: 10.1093/pcmedi/pbab008. eCollection 2021 Jun.

DOI:10.1093/pcmedi/pbab008
PMID:35694153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8982619/
Abstract

Cancer cachexia (CC) is a complex metabolic syndrome that accelerates muscle wasting and affects up to 80% of patients with cancer; however, timely diagnostic methods and effective cures are lacking. Although a considerable number of studies have focused on the mechanism of CC-induced muscle atrophy, few novel therapies have been applied in the last decade. In recent years, noncoding RNAs (ncRNAs) have attracted great attention as many differentially expressed ncRNAs in cancer cachectic muscles have been reported to participate in the inhibition of myogenesis and activation of proteolysis. In addition, extracellular vesicles (EVs), which function as ncRNA carriers in intercellular communication, are closely involved in changing ncRNA expression profiles in muscle and promoting the development of muscle wasting; thus, EV-related ncRNAs may represent potential therapeutic targets. This review comprehensively describes the process of ncRNA transmission through EVs and summarizes the pathways and targets of ncRNAs that lead to CC-induced muscle atrophy.

摘要

癌症恶病质(CC)是一种复杂的代谢综合征,会加速肌肉萎缩,影响多达80%的癌症患者;然而,目前缺乏及时的诊断方法和有效的治疗方法。尽管大量研究聚焦于CC诱导肌肉萎缩的机制,但在过去十年中几乎没有应用新的治疗方法。近年来,非编码RNA(ncRNAs)备受关注,因为据报道,癌症恶病质肌肉中许多差异表达的ncRNAs参与抑制肌生成和激活蛋白水解。此外,细胞外囊泡(EVs)作为细胞间通讯中的ncRNA载体,密切参与改变肌肉中的ncRNA表达谱并促进肌肉萎缩的发展;因此,与EV相关的ncRNAs可能代表潜在的治疗靶点。本综述全面描述了ncRNA通过EVs的传递过程,并总结了导致CC诱导肌肉萎缩的ncRNAs的途径和靶点。