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探索异质性:深入研究癌症恶病质的临床前模型。

Exploring heterogeneity: a dive into preclinical models of cancer cachexia.

机构信息

Cachexia Research Laboratory, Exercise Science Research Center, Department of Health, Human Performance and Recreation, University of Arkansas, Fayetteville, Arkansas, United States.

出版信息

Am J Physiol Cell Physiol. 2024 Aug 1;327(2):C310-C328. doi: 10.1152/ajpcell.00317.2024. Epub 2024 Jun 10.

DOI:10.1152/ajpcell.00317.2024
PMID:38853648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11427020/
Abstract

Cancer cachexia (CC) is a multifactorial and complex syndrome experienced by up to 80% of patients with cancer and implicated in ∼40% of cancer-related deaths. Given its significant impact on patients' quality of life and prognosis, there has been a growing emphasis on elucidating the underlying mechanisms of CC using preclinical models. However, the mechanisms of cachexia appear to differ across several variables including tumor type and model and biologic variables such as sex. These differences may be exacerbated by variance in experimental approaches and data reporting. This review examines literature spanning from 2011 to March 2024, focusing on common preclinical models of CC, including Lewis Lung Carcinoma, pancreatic KPC, and colorectal colon-26 and models. Our analysis reveals considerable heterogeneity in phenotypic outcomes, and investigated mechanisms within each model, with particular attention to sex differences that may be exacerbated through methodological differences. Although searching for unified mechanisms is critical, we posit that effective treatment approaches are likely to leverage the heterogeneity presented by the tumor and pertinent biological variables to direct specific interventions. In exploring this heterogeneity, it becomes critical to consider methodological and data reporting approaches to best inform further research.

摘要

癌症恶病质(CC)是一种多因素、复杂的综合征,高达 80%的癌症患者会经历这种综合征,并与约 40%的癌症相关死亡有关。鉴于其对患者生活质量和预后的重大影响,人们越来越重视使用临床前模型阐明 CC 的潜在机制。然而,恶病质的机制似乎因肿瘤类型和模型以及生物变量(如性别)等多种变量而有所不同。这些差异可能因实验方法和数据报告的差异而加剧。本综述考察了 2011 年至 2024 年 3 月的文献,重点关注常见的 CC 临床前模型,包括 Lewis 肺癌、胰腺 KPC 和结直肠结肠-26 和 模型。我们的分析揭示了表型结果存在相当大的异质性,以及每个模型中调查的机制,特别关注可能通过方法学差异加剧的性别差异。虽然寻找统一的机制至关重要,但我们认为有效的治疗方法可能利用肿瘤和相关生物学变量呈现的异质性来指导特定的干预措施。在探索这种异质性时,必须考虑方法学和数据报告方法,以最好地为进一步的研究提供信息。

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本文引用的文献

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Muscle weakness and mitochondrial stress occur before severe metastasis in a novel mouse model of ovarian cancer cachexia.在一种新型卵巢癌恶病质小鼠模型中,肌肉无力和线粒体应激发生在严重转移之前。
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Advancements and future directions in : a 2024 editorial update.《进展与未来方向:2024年编辑更新》
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Transcriptional analysis of cancer cachexia: conserved and unique features across preclinical models and biological sex.癌症恶病质的转录组学分析:临床前模型和生物性别之间的保守和独特特征。
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Cells. 2024 Sep 27;13(19):1620. doi: 10.3390/cells13191620.
优化胰腺癌小鼠模型以模拟转移和恶病质的人类表型。
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