Rapid Communication
Copyright ©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Feb 14, 2006; 12(6): 966-970
Published online Feb 14, 2006. doi: 10.3748/wjg.v12.i6.966
Figure 1
Figure 1 Expression of E-cadherin in SV40-immortalized Ges-1 and gastric cancer cell lines. Negative staining of E-cadherin in Ges-1 and MGC-803 was shown on immunofluorescent micrographs.
Figure 2
Figure 2 Expression of N-cadherin in SV40-immortalized Ges-1 and gastric cancer cell lines. A: Distribution of N-cadherin fluorescence on cell membranes in Ges-1 and gastric cancer cell lines; B: A band of 135 ku N-cadherin protein detected by Western blotting of N-cadherin; C: N-cadherin mRNA expression shown by RT-PCR.
Figure 3
Figure 3 Expression of α- and β-catenins in Ges-1 and gastric cancer cell lines. A: Distribution of α- and β-catenin fluorescence on cell membranes and cell-cell borders in Ges-1 and MGC-803; B: Reactive bands at 102 ku and 94 ku of α- and β-catenins in Ges-1 and cancer cell lines.
Figure 4
Figure 4 Expression of E-cadherin transcription repressors (snail, slug) and N-cadherin activator (twist) in Ges-1 and gastric cancer cell lines.