Literature DB >> 33783983

Phenotypic features of cancer cachexia-related loss of skeletal muscle mass and function: lessons from human and animal studies.

Agnès Martin1, Damien Freyssenet1.   

Abstract

Cancer cachexia is a complex multi-organ catabolic syndrome that reduces mobility, increases fatigue, decreases the efficiency of therapeutic strategies, diminishes the quality of life, and increases the mortality of cancer patients. This review provides an exhaustive and comprehensive analysis of cancer cachexia-related phenotypic changes in skeletal muscle at both the cellular and subcellular levels in human cancer patients, as well as in animal models of cancer cachexia. Cancer cachexia is characterized by a major decrease in skeletal muscle mass in human and animals that depends on the severity of the disease/model and the localization of the tumour. It affects both type 1 and type 2 muscle fibres, even if some animal studies suggest that type 2 muscle fibres would be more prone to atrophy. Animal studies indicate an impairment in mitochondrial oxidative metabolism resulting from a decrease in mitochondrial content, an alteration in mitochondria morphology, and a reduction in mitochondrial metabolic fluxes. Immuno-histological analyses in human and animal models also suggest that a faulty mechanism of skeletal muscle repair would contribute to muscle mass loss. An increase in collagen deposit, an accumulation of fat depot outside and inside the muscle fibre, and a disrupted contractile machinery structure are also phenotypic features that have been consistently reported in cachectic skeletal muscle. Muscle function is also profoundly altered during cancer cachexia with a strong reduction in skeletal muscle force. Even though the loss of skeletal muscle mass largely contributes to the loss of muscle function, other factors such as muscle-nerve interaction and calcium handling are probably involved in the decrease in muscle force. Longitudinal analyses of skeletal muscle mass by imaging technics and skeletal muscle force in cancer patients, but also in animal models of cancer cachexia, are necessary to determine the respective kinetics and functional involvements of these factors. Our analysis also emphasizes that measuring skeletal muscle force through standardized tests could provide a simple and robust mean to early diagnose cachexia in cancer patients. That would be of great benefit to cancer patient's quality of life and health care systems. © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

Entities:  

Keywords:  Cancer cachexia; Fibre type; Fibrosis; Force; Metabolism; Regeneration; Skeletal muscle

Year:  2021        PMID: 33783983     DOI: 10.1002/jcsm.12678

Source DB:  PubMed          Journal:  J Cachexia Sarcopenia Muscle        ISSN: 2190-5991            Impact factor:   12.910


  11 in total

1.  Tumours block protective muscle and nerve signals to cause cachexia.

Authors:  Teresa A Zimmers
Journal:  Nature       Date:  2021-10       Impact factor: 69.504

2.  Inflammation and Wasting of Skeletal Muscles in Kras-p53-Mutant Mice with Intraepithelial Neoplasia and Pancreatic Cancer-When Does Cachexia Start?

Authors:  Wulf Hildebrandt; Jan Keck; Simon Schmich; Gabriel A Bonaterra; Beate Wilhelm; Hans Schwarzbach; Anna Eva; Mirjam Bertoune; Emily P Slater; Volker Fendrich; Ralf Kinscherf
Journal:  Cells       Date:  2022-05-11       Impact factor: 7.666

3.  Pectoralis major muscle atrophy is associated with mitochondrial energy wasting in cachectic patients with gastrointestinal cancer.

Authors:  Adeline Dolly; Thierry Lecomte; Nicolas Tabchouri; Morgane Caulet; Nicolas Michot; Benjamin Anon; Romain Chautard; Yoann Desvignes; Mehdi Ouaissi; Gaëlle Fromont-Hankard; Jean-François Dumas; Stéphane Servais
Journal:  J Cachexia Sarcopenia Muscle       Date:  2022-03-22       Impact factor: 12.063

4.  Silibinin Alleviates Muscle Atrophy Caused by Oxidative Stress Induced by Cisplatin through ERK/FoxO and JNK/FoxO Pathways.

Authors:  Meng-Yi Chi; Hong Zhang; Ya-Xian Wang; Xi-Peng Sun; Quan-Jun Yang; Cheng Guo
Journal:  Oxid Med Cell Longev       Date:  2022-01-20       Impact factor: 6.543

5.  Phosphorylation of Dynamin-Related Protein 1 (DRP1) Regulates Mitochondrial Dynamics and Skeletal Muscle Wasting in Cancer Cachexia.

Authors:  Xiangyu Mao; Yihua Gu; Xiangyu Sui; Lei Shen; Jun Han; Haiyu Wang; Qiulei Xi; Qiulin Zhuang; Qingyang Meng; Guohao Wu
Journal:  Front Cell Dev Biol       Date:  2021-08-05

Review 6.  Cachectic muscle wasting in acute myeloid leukaemia: a sleeping giant with dire clinical consequences.

Authors:  Dean G Campelj; Cara A Timpani; Emma Rybalka
Journal:  J Cachexia Sarcopenia Muscle       Date:  2021-12-08       Impact factor: 12.910

7.  Activin A Causes Muscle Atrophy through MEF2C-Dependent Impaired Myogenesis.

Authors:  Audrey Loumaye; Pascale Lause; Xiaoling Zhong; Teresa A Zimmers; Laure B Bindels; Jean-Paul Thissen
Journal:  Cells       Date:  2022-03-25       Impact factor: 6.600

8.  Cachexia index as a potential biomarker for cancer cachexia and a prognostic indicator in diffuse large B-cell lymphoma.

Authors:  Se-Il Go; Mi Jung Park; Sungwoo Park; Myoung Hee Kang; Hoon-Gu Kim; Jung Hun Kang; Jung Hoon Kim; Gyeong-Won Lee
Journal:  J Cachexia Sarcopenia Muscle       Date:  2021-10-21       Impact factor: 12.910

9.  Chemotherapy impairs skeletal muscle mitochondrial homeostasis in early breast cancer patients.

Authors:  Joris Mallard; Elyse Hucteau; Anne-Laure Charles; Laura Bender; Claire Baeza; Mathilde Pélissie; Philippe Trensz; Carole Pflumio; Michal Kalish-Weindling; Bernard Gény; Roland Schott; Fabrice Favret; Xavier Pivot; Thomas J Hureau; Allan F Pagano
Journal:  J Cachexia Sarcopenia Muscle       Date:  2022-04-04       Impact factor: 12.063

Review 10.  Pathological features of tissues and cell populations during cancer cachexia.

Authors:  Daniela Di Girolamo; Shahragim Tajbakhsh
Journal:  Cell Regen       Date:  2022-04-20
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