Liver Cancer
Copyright ©The Author(s) 2004.
World J Gastroenterol. May 15, 2004; 10(10): 1402-1408
Published online May 15, 2004. doi: 10.3748/wjg.v10.i10.1402
Figure 1
Figure 1 Cultured human liver cancer vascular endothelia. A: Morphology of cultured human liver cancer vascular endothelial cells; B: Uptake of Ac-LDL; C: Electron microscope for fenestration.
Figure 2
Figure 2 Immunofluorescence analysis of endothelial cells stained with the sera diluted 1:5000 isolated from the mice immunized with HLCVECs. A: HLCVECs; B: Activated HUVECs; C: HUVECs.
Figure 3
Figure 3 Inhibition of the HLCVECs proliferation by HLCVECs immunized murine serum from 1 of 6 immunized mice and 1 of 4 non-immunized mice. Points are the average of three wells.
Figure 4
Figure 4 Cell cycle analysis of HLCVECs after treatment with immune sera or non-immune sera. A: HLCVECs treated with immune sera for 6 h; B: HLCVECs treated with non-immune sera for 6 h.
Figure 5
Figure 5 Positive dots of phage clone of screening by immune sera. A: The first cycle of screening by immune sera; B: The second cycle of screening by immune sera.
Figure 6
Figure 6 Electrophoresis analysis of enzymatic digestion of SEREX positive clones. M, λHind III marker, from above to below: 20130, 9416, 6557, 4316, 2322, 2027, 564 bp; Lanes 1-8, positive clones digested with EcoR I and Xhol I.