Upregulation of IL-6, IL-8 and CXCL-1 production in dermal fibroblasts by normal/malignant epithelial cells in vitro: Immunohistochemical and transcriptomic analyses
Language English Country Great Britain, England Media print
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
23043537
DOI
10.1111/boc.201200018
Knihovny.cz E-resources
- MeSH
- Chemokine CXCL1 biosynthesis genetics MeSH
- Epithelial-Mesenchymal Transition genetics MeSH
- Epithelial Cells metabolism pathology MeSH
- Fibroblasts metabolism pathology MeSH
- Immunohistochemistry MeSH
- Interleukin-6 biosynthesis genetics MeSH
- Interleukin-8 biosynthesis genetics MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- Neoplasm Proteins biosynthesis genetics MeSH
- Neoplasms, Glandular and Epithelial metabolism pathology MeSH
- Gene Expression Regulation, Neoplastic * MeSH
- Dermis metabolism pathology MeSH
- Gene Expression Profiling MeSH
- Transcriptome genetics MeSH
- Up-Regulation genetics MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Chemokine CXCL1 MeSH
- CXCL1 protein, human MeSH Browser
- CXCL8 protein, human MeSH Browser
- IL6 protein, human MeSH Browser
- Interleukin-6 MeSH
- Interleukin-8 MeSH
- Neoplasm Proteins MeSH
BACKGROUND INFORMATION: Considering an analogy between wound healing and tumour progression, we studied chemokine and cytokine transcription and expression in normal fibroblasts by co-culture and in situ. RESULTS: Whole-genome transcriptome profiling revealed strong upregulation for the interleukin (IL)-6, IL-8 and the chemokine CXCL-1 in in vitro co-cultures of normal fibroblasts with either normal or malignant epithelial cells compared to fibroblast cultures. The same ILs/chemokines were distinctly upregulated in clinical samples of squamous cell carcinoma when compared with paired normal mucosae. Analysis of culture supernatants showed that during the course of co-culture of the fibroblasts with the epithelial cells, IL-6, IL-8 and CXCL-1 were secreted to the culture medium. Experiments with addition of any of the proteins to the culture medium supported the notion that these ILs/chemokines strongly contributed to maintenance of a low-differentiation phenotype of epithelial cells, evaluated by the detection of keratin-8. Simultaneous addition of all factors increased the extent of the effect. These studies were extended by experiments with epithelial cells, either cultured in medium conditioned by preceding use for malignant keratinocytes without and in the presence of normal or cancer-associated fibroblasts or medium containing antibodies against IL-6, IL-8 and CXCL-1. CONCLUSIONS: Our results indicate an analogy between wound healing and tumour growth, support the importance of epithelial-mesenchymal interaction in this model system and establish a potential bio-inspired anticancer therapy.
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