Abstract:Objective To transfect siRNA into Hep2 cells for knocking down plateletderived growth factor (PDGFB) mRNA, and to detect its effect on the proliferation of Hep2 cells. Methods Four groups of PDGFB targeted siRNA were transfected into Hep2 cells with lipofectamine 2000 as vector. The expression of PDGFB mRNA and PDGFB protein was detected by realtime PCR and Western Blot respectively. MTT was used for detecting the inhibitory rates of proliferation. Results Realtime PCR showed that the expression of PDGFB mRNAs in siRNA2, siRNA3, and siRNA4 groups was inhibited with the highest inhibitory rate in siRNA2 group. The differences of the expression levels of PDGFB mRNAs in siRNA2, siRNA3, and siRNA4 groups and those of the siRNA2, the negative control and the empty liposome groups were statistically significant (P<0.05). Western Blot showed that the expression of PDGFB protein in siRNA1, siRNA2, and siRNA3 groups declined with the lowest expression in siRNA2 group. The expression of PDGFB protein in siRNA4, the negative control and the empty liposome groups were not inhibited. The MTT assay showed that siRNA1, siRNA2, and siRNA3 could inhibit cell proliferation with the most obvious inhibitory effect on siRNA2. The differences of the inhibitory rates of cell proliferation in siRNA1, siRNA2, and siRNA3 groups and those of the siRNA4, the negative control and the empty liposome groups were statistically significant (P<0.05). Conclusion siRNAs targeting PDGFB can downregulate the expression of PDGFB gene and the knockdown of PDGFB mRNA can inhibit the proliferation of Hep2 cells effectually.