Previous studies from our laboratory have demonstrated that human mela
noma cell lines and tumors expressed high levels of the extracellular
protein SPARC. In order to demonstrate its role in human melanoma prog
ression, IIB-MEL-LES human melanoma cells were transfected with SPARC
full length c-DNA in the antisense orientation. In vivo studies demons
trated that all the control mice injected with parental cells develope
d tumors, while none of the mice injected with cells obtained from thr
ee different clones with diminished levels of SPARC expression, develo
ped tumors. These studies suggest that SPARC may play a key role in hu
man melanoma progression.