Comparative analysis of IL-8 and CXCL-1 production by normal and cancer stromal fibroblasts
Jazyk angličtina Země Česko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
23890481
PII: file/5691/FB2013A0018.pdf
Knihovny.cz E-zdroje
- MeSH
- buňky stromatu metabolismus MeSH
- chemokin CXCL1 metabolismus MeSH
- fibroblasty metabolismus MeSH
- hojení ran fyziologie MeSH
- interleukin-8 metabolismus MeSH
- keratinocyty fyziologie MeSH
- kokultivační techniky MeSH
- kultivační média speciální MeSH
- kultivované buňky MeSH
- lidé MeSH
- nádorové proteiny metabolismus MeSH
- nádory hypofaryngu metabolismus patologie MeSH
- nádory kůže metabolismus patologie MeSH
- rychlost sekrece MeSH
- škára cytologie MeSH
- spinocelulární karcinom metabolismus patologie MeSH
- upregulace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- chemokin CXCL1 MeSH
- CXCL1 protein, human MeSH Prohlížeč
- interleukin-8 MeSH
- kultivační média speciální MeSH
- nádorové proteiny MeSH
It has been shown that fibroblasts within the stroma of malignant tumours can affect the tumour's biological character, influencing such properties as local aggressiveness and metastasis potential. This influence is asserted via paracrine secretion of multiple cell factors, including chemokines. This study demonstrates that both normal keratinocytes and cancer cells can stimulate the secretion of chemokines IL-8 and CXCL-1 from normal dermal fibroblasts and stromal fibroblasts from squamous cell carcinoma. The effect of epithelia on normal fibroblasts leads to a transient secretory change, in contrast to stromal fibroblasts which generate a more prolonged one. This observation demonstrates that stimulated expression of both IL-8 and CXCL-1 is not specific to cancer, supporting the hypothesis that similar mechanisms exist between wound healing and oncogenesis. It also shows that stromal fibroblasts isolated from a tumour have significantly different features from normal fibroblasts.
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