The metabolic basis of cancer-related fatigue

IF 7.9 1区 医学 Q1 BEHAVIORAL SCIENCES Neuroscience and Biobehavioral Reviews Pub Date : 2025-02-01 DOI:10.1016/j.neubiorev.2025.106035
Robert Dantzer , Brandon Chelette , Elisabeth G. Vichaya , A. Phillip West , Aaron Grossberg
{"title":"The metabolic basis of cancer-related fatigue","authors":"Robert Dantzer ,&nbsp;Brandon Chelette ,&nbsp;Elisabeth G. Vichaya ,&nbsp;A. Phillip West ,&nbsp;Aaron Grossberg","doi":"10.1016/j.neubiorev.2025.106035","DOIUrl":null,"url":null,"abstract":"<div><div>Although we are all familiar with the sensation of fatigue, there are still profound divergences on what it represents and its mechanisms. Fatigue can take various forms depending on the condition in which it develops. Cancer-related fatigue is considered a symptom of exhaustion that is often present at the time of diagnosis, increases in intensity during cancer therapy, and does not always recede after completion of treatment. It is usually attributed to the inflammation induced by damage-associated molecular patterns released by tumor cells during cancer progression and in response to its treatment. In this review, we argue that it is necessary to go beyond the symptoms of fatigue to understand its nature and mechanisms. We propose to consider fatigue as a psychobiological process that regulates the behavioral activities an organism engages in to satisfy its needs, according to its physical ability to do so and to the capacity of its intermediary metabolism to exploit the resources procured by these activities. This last aspect is critical as it implies that these metabolic aspects need to be considered to understand fatigue. Based on the findings we have accumulated over several years of studying fatigue in diverse murine models of cancer, we show that energy metabolism plays a key role in the development and persistence of this condition. Cancer-related fatigue is dependent on the energy requirements of the tumor and the negative impact of cancer therapy on the mitochondrial function of the host. When inflammation is present, it adds to the organism’s energy expenses. The organism needs to adjust its metabolism to the different forms of cellular stress it experiences thanks to specialized communication factors known as mitokines that act locally and at a distance from the cells in which they are produced. They induce the subjective, behavioral, and metabolic components of fatigue by acting in the brain. Therefore, the targeting of mitokines and their brain receptors offers a window of opportunity to treat fatigue when it is no longer adaptive but an obstacle to the quality of life of cancer survivors.</div></div>","PeriodicalId":56105,"journal":{"name":"Neuroscience and Biobehavioral Reviews","volume":"169 ","pages":"Article 106035"},"PeriodicalIF":7.9000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience and Biobehavioral Reviews","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0149763425000351","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Although we are all familiar with the sensation of fatigue, there are still profound divergences on what it represents and its mechanisms. Fatigue can take various forms depending on the condition in which it develops. Cancer-related fatigue is considered a symptom of exhaustion that is often present at the time of diagnosis, increases in intensity during cancer therapy, and does not always recede after completion of treatment. It is usually attributed to the inflammation induced by damage-associated molecular patterns released by tumor cells during cancer progression and in response to its treatment. In this review, we argue that it is necessary to go beyond the symptoms of fatigue to understand its nature and mechanisms. We propose to consider fatigue as a psychobiological process that regulates the behavioral activities an organism engages in to satisfy its needs, according to its physical ability to do so and to the capacity of its intermediary metabolism to exploit the resources procured by these activities. This last aspect is critical as it implies that these metabolic aspects need to be considered to understand fatigue. Based on the findings we have accumulated over several years of studying fatigue in diverse murine models of cancer, we show that energy metabolism plays a key role in the development and persistence of this condition. Cancer-related fatigue is dependent on the energy requirements of the tumor and the negative impact of cancer therapy on the mitochondrial function of the host. When inflammation is present, it adds to the organism’s energy expenses. The organism needs to adjust its metabolism to the different forms of cellular stress it experiences thanks to specialized communication factors known as mitokines that act locally and at a distance from the cells in which they are produced. They induce the subjective, behavioral, and metabolic components of fatigue by acting in the brain. Therefore, the targeting of mitokines and their brain receptors offers a window of opportunity to treat fatigue when it is no longer adaptive but an obstacle to the quality of life of cancer survivors.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
癌症相关疲劳的代谢基础。
虽然我们都熟悉疲劳的感觉,但在它代表什么和它的机制上仍然存在深刻的分歧。疲劳可以有不同的形式,这取决于它的发展条件。癌症相关疲劳被认为是一种疲惫的症状,通常在诊断时出现,在癌症治疗期间强度增加,并且在治疗完成后并不总是消退。它通常归因于肿瘤细胞在癌症进展过程中释放的与损伤相关的分子模式引起的炎症以及对其治疗的反应。在这篇综述中,我们认为有必要超越疲劳的症状来了解其性质和机制。我们建议将疲劳视为一种心理生物学过程,根据机体的生理能力和中间代谢利用这些活动所获得的资源的能力,调节机体为满足其需求而进行的行为活动。最后一个方面是至关重要的,因为它意味着需要考虑这些代谢方面来理解疲劳。基于我们多年来在不同癌症小鼠模型中对疲劳的研究积累的发现,我们表明能量代谢在这种情况的发展和持续中起着关键作用。癌症相关疲劳取决于肿瘤的能量需求和癌症治疗对宿主线粒体功能的负面影响。当炎症出现时,它会增加机体的能量消耗。生物体需要调整其新陈代谢以适应不同形式的细胞应激,这要归功于被称为分裂因子的特殊通讯因子,它在局部起作用,并与产生它们的细胞保持一定距离。它们通过作用于大脑,诱发疲劳的主观、行为和代谢成分。因此,靶向分裂因子及其脑受体为治疗疲劳提供了一个机会之窗,当疲劳不再具有适应性时,它是癌症幸存者生活质量的障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
14.20
自引率
3.70%
发文量
466
审稿时长
6 months
期刊介绍: The official journal of the International Behavioral Neuroscience Society publishes original and significant review articles that explore the intersection between neuroscience and the study of psychological processes and behavior. The journal also welcomes articles that primarily focus on psychological processes and behavior, as long as they have relevance to one or more areas of neuroscience.
期刊最新文献
Serotonergic psychedelics as epigenetic modulators: A paradigm shift in Alzheimer's disease therapeutics. On human synchrony: a systematic review of the origins of physiological and neural synchrony in parent-infant dyads (0-12 months). Energy Deficit Hyperactivity Disorder (EDHD): A Neurobiological Energy Dysregulation Model for ADHD. Rethinking Anorexia Nervosa Through the Lens of Control, Compulsion and Reward: Neurobiological Insights Into Addiction-Like Features via the Dopaminergic, Endocannabinoid, and Orexinergic Systems - A Narrative Review. Seeing without eyes: Relation between visual mental imagery and visual hallucinations.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1