Pharmacologic treatment of desmoid tumors in familial adenomatous polyposis: results of an in vitro study.

Abstract

BACKGROUND:

Desmoid tumors (DTs), the result of an abnormal proliferation of connective tissue, occur frequently in familial adenomatous polyposis. Treatment of DT is difficult because of the high rate of recurrence after operation. Recently, antiestrogens and nonsteroidal antiinflammatory drugs have been used with good results as inhibitors of DT cell proliferation.

METHODS:

In this report we performed in vitro studies on cultured desmoid cells and skin fibroblasts of four patients who underwent surgical resection of DT and normal skin biopsy. We evaluated the expression of estrogen receptors and the mitogenic effect of 17 beta-estradiol and sulindac, a nonsteroidal antiinflammatory compound, on cell proliferation and collagen synthesis of desmoid cells.

RESULTS:

Proliferation and collagen synthesis of desmoid cells were stimulated by 17 beta-estradiol, and tamoxifen, an antiestrogenic compound, inhibited this effect. Desmoid cells also expressed estrogen receptors. Moreover, growth of desmoid cells from one of the patients was inhibited by sulindac.

CONCLUSIONS:

The in vitro evaluation of drug responsiveness in patients operated on for DT could be used as both a prognostic tool in the natural history of DT and in addressing pharmacologic therapy in this disorder.

• Authors: F Tonelli, R Valanzano, M L Brandi
• Journal: Surgery (Surgery) Vol. 115 Issue 4 Pg. 473-9 (Apr 1994) ISSN: 0039-6060 [Print] United States
• PMID: 8165538 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Receptors, Estrogen
• Sulindac
• Estradiol
• Collagen

Topics

• Adenomatous Polyposis Coli (drug therapy, metabolism, pathology)
• Adolescent
• Adult
• Cell Division (drug effects)
• Child
• Collagen (biosynthesis)
• Estradiol (pharmacology)
• Fibromatosis, Aggressive (drug therapy, metabolism, pathology)
• Humans
• Receptors, Estrogen (metabolism)
• Sulindac (pharmacology)
• Tumor Cells, Cultured