Cancer cell expression of urokinase-type plasminogen activator receptor mRNA in squamous cell carcinomas of the skin

In this study we have used in situ hybridization with radiolabeled antisens e RNA probes to examine the expression of mRNA for urokinase-type plasminog en activator and its receptor in histologic samples of squamous cell (n = 7 ) and basal cell (n = 7) carcinomas of the skin. Messenger RNA for both uro kinase-type plasminogen activator and its receptor were expressed in all of the squamous cell carcinomas, but could not be detected in the basal cell carcinomas. In all of the seven squamous cell carcinomas a signal for uroki nase-type plasminogen activator receptor mRNA was detected focally in well- differentiated cancer cells surrounding keratinized pearls, and in four spe cimens urokinase-type plasminogen activator receptor mRNA was in addition e xpressed by cancer cells at the edge of invasively growing strands of tumor . Urokinase-type plasminogen activator mRNA expression was found in virtual ly all the cancer cells of the squamous cell carcinomas, and importantly we found, by hybridizations for urokinase-type plasminogen activator and its receptor mRNA on adjacent sections of squamous cell carcinomas, that it was exactly the invading cancer cells that simultaneously expressed both these components required for plasmin-mediated proteolysis at the cell surface. We have previously shown that both urokinase-type plasminogen activator and its receptor mRNA are expressed by the leading-edge keratinocytes in regen erating epidermis during mouse skin wound healing, and that wound healing i s impaired in mice made deficient in plasminogen by targeted gene disruptio n. We propose that there are similarities between the mechanisms of generat ion and regulation of extracellular proteolysis during skin re-epithelializ ation and squamous cell carcinoma invasion. The ability of the squamous car cinoma cells to mimic the ''invasive'' phenotype of re-epithelializing kera tinocytes may be one of the factors that make squamous cell carcinomas more aggressive tumors than basal cell carcinomas.