Cancer cachexia: A tumor-driven disorder of whole-body homeostasis

Cancer cachexia is a systemic metabolic syndrome driven by tumor-induced disruption of whole-body homeostasis. Characterized by skeletal muscle atrophy and adipose tissue loss, cachexia leads to functional decline, impaired quality of life, reduced treatment tolerance, and poor survival across multiple malignancies. Emerging evidence indicates that cachexia arises from complex and dynamic interactions between tumors and host organ systems, including immune, metabolic, endocrine, and neural networks, that collectively reshape energy balance, immune function, and tissue integrity. Despite its profound clinical impact, effective therapies remain limited, reflecting incomplete mechanistic understanding and the absence of integrated clinical frameworks. Here, we review recent advances in cachexia biology, including tumor-host signaling, multiorgan metabolic remodeling, and neuroendocrine regulation. We further propose a tumor-centric framework in which cachexia represents a progressive collapse of systemic homeostasis and outline translational strategies to guide mechanism-informed therapeutic interventions.

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Publication Details

Journal
Cancer Cell
Published
2026-04-16
DOI
https://doi.org/10.1016/j.ccell.2026.03.012
Primary Topic
Nutrition and Health in Aging
Type
article
Field-Weighted Citation Impact
0.00

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article

Cancer cachexia: A tumor-driven disorder of whole-body homeostasis

Tobias Janowitz, Denis C. Guttridge, Min Li, Ryan D. Nipp et al.
Cancer Cell
Nutrition and Health in Aging
article

Cancer cachexia: A tumor-driven disorder of whole-body homeostasis

Tobias Janowitz, Denis C. Guttridge, Min Li, Ryan D. Nipp, Yuqing Zhang, Yi-Ping Li
article en

Abstract

Cancer cachexia is a systemic metabolic syndrome driven by tumor-induced disruption of whole-body homeostasis. Characterized by skeletal muscle atrophy and adipose tissue loss, cachexia leads to functional decline, impaired quality of life, reduced treatment tolerance, and poor survival across multiple malignancies. Emerging evidence indicates that cachexia arises from complex and dynamic interactions between tumors and host organ systems, including immune, metabolic, endocrine, and neural networks, that collectively reshape energy balance, immune function, and tissue integrity. Despite its profound clinical impact, effective therapies remain limited, reflecting incomplete mechanistic understanding and the absence of integrated clinical frameworks. Here, we review recent advances in cachexia biology, including tumor-host signaling, multiorgan metabolic remodeling, and neuroendocrine regulation. We further propose a tumor-centric framework in which cachexia represents a progressive collapse of systemic homeostasis and outline translational strategies to guide mechanism-informed therapeutic interventions.

Cancer CellVol. 44(5)
Medical University of South Carolina (US), Cold Spring Harbor Laboratory (US), University of Oklahoma Health Sciences Center (US), The University of Texas Health Science Center at Houston (US)
William and Ella Owens Medical Research Foundation, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 26%
Nutrition and Health in Aging
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