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Table 1 Mediators and mechanisms of skeletal muscle loss in cancer cachexia: correlation of findings in animal models and humans

From: Molecular pathways leading to loss of skeletal muscle mass in cancer cachexia – can findings from animal models be translated to humans?

 

Animal models

Humans

TNF-α

++

+/−

Yoshida hepatoma/sarcoma, LLC, Leydig cell tumor, Morris hepatoma

Various types of solid tumors

TRAF-6

+

+

LLC

Gastric cancer

IL-6

++

+/−

C26, Morris hepatoma, ApcMin/+

Various types of solid tumors

IL-1

+

+/−

Methylcholanthrene-induced Sarcoma, Prostate ADK

Various types of solid tumors

INF-γ

+

+/−

MAC16

Various types of solid tumors

Myostatin/ TGF-ß

++

+

C26, MAC16

Gastric cancer

PIF

+

+/−

MAC16

GIT cancers

Angiotensin II

+

+

C26

NSCLC, congestive heart failure

Ubiquitin-Proteasome system

++

+

C26, Yoshida hepatoma, LLC

GIT cancers

Autophagy-lysosomal system

+

+

C26, Yoshida hepatoma, LLC

Lung cancer

IGF-1/Pi3K/Akt/mTOR

+/−

+/−

C26, ApcMin/+

Various types of solid tumors

MRFs (Myo D, Pax7)

+

+

C26

Pancreatic cancer

  1. + role confirmed in few studys
  2. ++ role confirmed in many studys
  3. +/− role not confirmed/inconsistent results
  4. Abbreviations: TNF tumor necrosis factor, LLC Lewis lung cell carcinoma, TRAF TNF-receptor adaptor protein, IL interleukin, INF interferon, TGF transforming growth factor, PIF proteolysis inducing factor, IGF insulin like growth factor, MRF muscle growth and regeneration factor