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Expression of basic fibroblast growth factor (bFGF) in Kaposi's sarcoma: an immunohistologic study
K Schulze-Osthoff1, S Goerdt, C Sorg
1Institute of Experimental Dermatology, University of Münster, F.R.G.
The Journal of Investigative Dermatology
|August 1, 1990
Summary
Basic fibroblast growth factor (bFGF) was not found in Kaposi's sarcoma (KS) tumor cells, challenging the autocrine growth hypothesis. This suggests KS proliferation may not be driven by self-produced bFGF.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Kaposi's sarcoma (KS) is a malignancy associated with various forms, including AIDS-related, classical, and pseudo-KS.
- Previous in vitro studies suggested that autocrine secretion of basic fibroblast growth factor (bFGF) might drive KS tumor cell proliferation.
Purpose of the Study:
- To investigate the in vivo expression of basic fibroblast growth factor (bFGF) in different types of Kaposi's sarcoma (KS).
- To determine if KS tumor cells exhibit autocrine secretion of bFGF.
Main Methods:
- Immunoperoxidase staining was performed on cryostat sections of ten KS cases (five AIDS-KS, one classical KS, four pseudo-KS).
- Affinity-purified anti-bFGF antibodies were used to detect bFGF antigen expression.
- Staining patterns were compared between KS tumor cells and normal skin biopsies.
Main Results:
- Basic fibroblast growth factor (bFGF) was strongly expressed in basal and suprabasal keratinocytes of normal skin.
- bFGF was generally absent or showed only very faint staining in the endothelial cells and spindle cells of the KS neoplasms.
- These findings contrast with previous in vitro observations.
Conclusions:
- The in vivo data strongly suggest that KS tumor cell proliferation is unlikely to be explained by an autocrine secretion mechanism of bFGF.
- The study provides evidence against the previously proposed autocrine hypothesis for KS growth.
- Further research is needed to elucidate the actual mechanisms driving KS proliferation in vivo.