The desmoplastic response to human breast carcinoma is a host myo®broblast-mediated collagenous response exhibiting synergistic e ects on tumor progression. Although many paracrine interactions between breast carcinoma cells and myo®broblasts have been characterized, the event(s) which initiate desmoplasia have remained unde®ned. Our studies utilized c-ras H transfected MCF-7 cells which overexpress ras p2l and which are weakly tumorigenic in ovariectomized nude mice. The xenografts are desmoplastic and comprised of 30% myo®broblasts and 60 mg/g of interstitial collagen. In situ hybridization studies of these xenografts reveal a stromal gene expression pattern (stromelysin-3, IGF-II and TIMP-1) identical to that observed in human tumor desmoplasia. 17-b estradiol increases c-ras H MCF-7 growth but abolishes desmoplasia. c-ras H MCF-7 in vitro constitutively produce myo®broblast mitogenic activity which competes with PDGF in a receptor binding assay. This myo®broblast mitogenic activity is unaltered by 17-b estradiol/tamoxifen pretreatment in vitro. Transfection of c-ras H MCF-7 with a PDGF-A dominant negative mutant, 1308, produced by site-directed mutagenesis (serine?cysteine 129 ) reduces both homo-and heterodimer secretion of PDGF by as much as 90% but does not interfere with the secretion of other growth factors. Clones with low PDGF, though tumorigenic, are nondesmoplastic. Our results suggest that breast carcinomasecreted PDGF is the major initiator of tumor desmoplasia. Oncogene (2000) 19, 4337 ± 4345.