Transforming growth factor-beta1 increases survival of human melanoma through stroma remodeling

Transforming growth factor (TGF)-beta is growth inhibitory for normal epithelial cells and melanocytes but can stimulate mesenchymal cells. Resistance to its inhibitory effects is characteristic of human melanoma, the growth of which may instead be promoted by TGF-beta, because its production is inc...

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Published in:Cancer research (Chicago, Ill.) Ill.), 2001-11, Vol.61 (22), p.8306-8316
Main Authors: Berking, C, Takemoto, R, Schaider, H, Showe, L, Satyamoorthy, K, Robbins, P, Herlyn, M
Format: Article
Language:English
Subjects:
Animals
Cell Communication - physiology
Cell Death - physiology
Cell Survival - physiology
Extracellular Matrix Proteins - biosynthesis
Female
Fibroblasts - pathology
Fibroblasts - physiology
Gene Expression
Gene Expression Profiling
Humans
Immunohistochemistry
Male
Melanoma - metabolism
Melanoma - pathology
Melanoma - secondary
Mice
Mice, SCID
Stromal Cells - metabolism
Stromal Cells - pathology
Transduction, Genetic
Transforming Growth Factor beta - biosynthesis
Transforming Growth Factor beta - genetics
Transforming Growth Factor beta - physiology
Transforming Growth Factor beta1
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Summary:Transforming growth factor (TGF)-beta is growth inhibitory for normal epithelial cells and melanocytes but can stimulate mesenchymal cells. Resistance to its inhibitory effects is characteristic of human melanoma, the growth of which may instead be promoted by TGF-beta, because its production is increased with melanoma progression. Whether TGF-beta has an autocrine function for melanoma cells or is important for paracrine stimulation of the tumor stroma is not known. In this study, TGF-beta1 was expressed in melanoma cells via adenoviral gene transfer, and tumor growth was analyzed in vitro, in human skin grafts, and in mixtures with fibroblasts that were injected s.c. into immunodeficient mice. The TGF-beta1 produced by the melanoma cells activated the fibroblasts to produce matrix within and around the tumor mass, whereas control tumors showed less stroma and more cell death. High expression of collagen, fibronectin, tenascin, and alpha2 integrin was detected in the TGF-beta1-expressing tumors by immunohistochemistry. Number and size of lung metastases were significantly increased. cDNA expression array analysis of TGF-beta1-transduced fibroblasts embedded in type I collagen and of TGF-beta1-transduced melanoma cells demonstrated induction of types XV, XVIII, and VI collagens, tenascin, plasminogen activator inhibitor-I, vascular endothelial growth factor, cysteine-rich fibroblast growth factor receptor-1, and platelet-derived growth factor receptor-beta, which could be linked to promotion of growth and survival in melanoma. These data suggest that remodeling of the neighboring stroma, which provides a supporting scaffolding and a positive feedback stimulation of tumor growth, is an important function of TGF-beta1 in melanoma.
ISSN:0008-5472