Specific effects of ras oncogene expression on the growth and histogenesis of human epidermal keratinocytes.

Little progress has been made in identifying specific regulatory pathways that might be affected in cells by a mutationally activated p21ras when its expression does not lead to complete transformation. We wished to determine whether a normal, diploid human epithelial cell in which activation of ras had occurred could be identified in culture and, furthermore, whether expression of a mutant p21ras in such an otherwise normal cell would result in abnormal histogenic behavior in vivo. Thus, we introduced the v-Ha-ras gene into an early passage culture of normal human epidermal keratinocytes via a defective retrovirus. We examined these genetically engineered cells for changes in growth and differentiation, both in culture and in the epithelium formed when cultures were grafted to the skin of nude mice. We have found that keratinocytes expressing p21v-ras are independent of epidermal growth factor (EGF)--a factor which is normally essential for progressive colony growth, but that they are otherwise indistinguishable in culture from normal cells. v-ras keratinocytes also secrete a factor possessing some specific biological activities of members of the fibroblast growth factor (FGF) family, but which is distinct from acidic and basic FGF. In short-term dermal grafts the v-ras cells form a non-invasive and normally differentiating epidermis. However, the cells express elevated levels of keratin 19, which is a characteristic of fetal epidermis and of premalignant lesions of some stratified squamous epithelia.