Liver Cancer
Copyright ©The Author(s) 2003.
World J Gastroenterol. Mar 15, 2003; 9(3): 474-478
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.474
Figure 1
Figure 1 pRcHCNS3-5’digested with Xbal. Lane M:DNA marker (GenerulerTM 100bpDNA). Lane: 1, 2, 3, 4 plasmid pRcHCNS3-5’ with 886bp fragment. ( × 100).
Figure 2
Figure 2 Colony formation of pRcHCNS3-5’ transfected QSG7701 cells in G418 ( × 100).
Figure 3
Figure 3 PCR analysis of DNA from QSG7701 transfected with pRcHCNS3-5’ and pRcCMV; Lane M: 100bp marker; Lane 1: pRcHCNS3-5’ transfected cells; Lane 2: pRcCMV transfected cells; Lane 3: QSG parental cells.
Figure 4
Figure 4 Immunohistochemistry analysis (S-P) of HCV N protein expression in pRcHCNS3-5’ transfected cells (up) and the negative control without positive signal (down) (×400).
Figure 5
Figure 5 Proliferation rate of cells transfected with pRcHCNS3-5’, pRcCMV and parental QSG7701cells.
Figure 6
Figure 6 Tumor development in nude mice, 6a, 6b, 6c and 6d show inoculated with pRcHCNS3-5’transfecting QSG7701 cells, HepG2 cells, QSG7701 cells transfected with pRcCMV and pa-rental QSG7701 cells, respectively.
Figure 7
Figure 7 pRcHCNS3-5’ induced hepatacellular carcinoma (7a HE×100, 7b HE×400), HCV NS3 (7c) and c-myc (7d) protein expressing in the tumor tissue by immunohistochemistry (S-P), the positive signals are both in cytoplasm ( × 400).