Ontology highlight
ABSTRACT: Background
Cancer cachexia-induced skeletal muscle fibrosis (SMF) impairs muscle regeneration, alters the muscle structure and function, reduces the efficacy of anticancer drugs, diminishes the patient's quality of life and shortens overall survival. RUNX family transcription factor 2 (Runx2), a transcription factor, and collagen type I alpha 1 chain (COL1A1), the principal constituent of SMF, have been linked previously, with Runx2 shown to directly modulate COL1A1 mRNA levels. l-Carnitine, a marker of cancer cachexia, can alleviate fibrosis in liver and kidney models; however, its role in cancer cachexia-associated fibrosis and the involvement of Runx2 in the process remain unexplored.Methods
Female C57 mice (48 weeks old) were inoculated subcutaneously with MC38 cells to
SUBMITTER: Lu Z
PROVIDER: S-EPMC11446711 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature