According to the autocrine hypothesis of cell growth,
tumors, in contrast to normal tissue, might simultaneously express both a
growth factor and its receptor, resulting in autoregulation and autostimulation of growth. In a related hypothesis, expression of either a
growth factor or receptor might allow a
tumor to escape exogenous controls on growth, and thereby correlate with malignant potential. Using immunohistochemistry, we investigated these hypotheses in 69 human soft tissue
tumors (STT) by assaying for the expression of
nerve growth factor and
receptor, epidermal growth factor and receptor and
platelet-derived growth factor. Both benign (B) and malignant (M) STT expressed a variety of factors and receptors. However, the frequency of any
growth factor expression (90% M versus 55% B, p = 0.002) and of multiple factors (59% M versus 24% B, p = 0.006) was significantly greater in malignant
tumors. Similarly, expression of any
growth factor receptor (73% M versus 31% B, p = 0.001) and of multiple receptors (35% M versus 3% B, p = 0.002) was significantly more frequent in malignant STT. In terms of the autocrine hypothesis,
growth factor/receptor co-expression was significantly more common in malignant STT (63% M versus 17% B, p = 0.0002). We conclude that (a) expression of both single and multiple
growth factors and receptors was significantly more frequent in malignant STT; (b) support for an autocrine growth mechanism through simultaneous factor/receptor co-expression can be found in both benign and malignant STT; (c) co-expression, however, was more frequent in the malignant
tumors; and (d) overall,
growth factor and receptor expression, as well as co-expression, was related to
biologic potential among human soft tissue
tumors.