Synthetic polyamine BPA-C8 inhibits TGF-β1-mediated conversion of human dermal fibroblast to myofibroblasts and establishment of galectin-1-rich extracellular matrix in vitro
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- Keywords
- actin, cancer, galectin, polycations, tenascin,
- MeSH
- Actins metabolism MeSH
- Fibroblasts drug effects pathology MeSH
- Galectin 1 metabolism MeSH
- Rats MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Myofibroblasts drug effects pathology MeSH
- Tumor Cells, Cultured MeSH
- Neoplasms drug therapy metabolism pathology MeSH
- Polyamines chemistry pharmacology MeSH
- Dermis cytology drug effects MeSH
- Transforming Growth Factor beta1 metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Actins MeSH
- Galectin 1 MeSH
- Polyamines MeSH
- Transforming Growth Factor beta1 MeSH
Cancer-associated fibroblasts (CAFs) play a role in the progression of malignant tumors. They are formed by conversion of fibroblasts to smooth muscle α-actin-positive (SMA-positive) myofibroblasts. Polyamines are known to change the arrangement of the actin cytoskeleton by binding to the anionic actin. We tested the effect of the synthetic polyamine BPA-C8 on the transition of human dermal fibroblasts to myofibroblasts induced either by TGF-β1 alone or by TGF-β1 together with adhesion/growth-regulatory galectin-1. Pre-existing CAFs, myofibroblasts from pancreatitis, and rat smooth muscle cells were also exposed to BPA-C8. BPA-C8 impaired myofibroblast formation from activated fibroblasts, but it had no effect on cells already expressing SMA. BPA-C8 also reduced the occurrence of an extracellular matrix around the activated fibroblasts. The reported data thus extend current insights into polyamine activity, adding interference with tumor progression to the tumor-promoting processes warranting study.
References provided by Crossref.org
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