Our previous studies have found that reducing expression of myeloid
zinc finger-1 (MZF-1) inhibited
protein kinase C alpha (PKCalpha) expression and decreased cell migration and invasion in human
hepatocellular carcinoma (HCC). In this study, we further investigated the role of MZF-1 in
tumorigenesis. The SK-Hep-1 HCC cells were transfected with the
antisense oligonucleotide (ODN) of MZF-1. The pretreated cells was then detected the
mRNA and
protein levels by RT-PCR and western blotting, and the cell growth was assayed by MTT. Meanwhile, the pretreated-SK-Hep-1 HCC cells were implanted subcutaneously into nude mice to observe the
tumor growth and calculated
tumor inhibitory rate. The results showed that, at the dosage of 5 microM, the antisense ODN MZF-1 suppressed both MZF-1 and PKCalpha productions by SK-Hep-1 HCC cells after cationic
liposome-mediated transfection, to 15% and 30% in control cultures of 0 microM dosage, respectively. The growth of SK-Hep-1 HCC cells was inhibited by the 2-5 microM doses of the antisense ODN MZF-1, whereas the control
reagent, the sense ODN MZF-1, showed no effects. In BALB/nude mice, SK-Hep-1 HCC cells pretreated with the 5 microM antisense ODN MZF-1 formed
tumors much smaller than the cells with sense ODN. The mean of inhibitory rate of
tumor growth was 71.2 +/- 8.6%, and the
tumor formation time was prolonged from 14 days to 26 days. These findings suggested the usefulness of antisense ODN MZF-1 as a new
reagent for
cancer therapy.