Original Article
Copyright ©2010 Baishideng.
World J Gastroenterol. Aug 21, 2010; 16(31): 3897-3904
Published online Aug 21, 2010. doi: 10.3748/wjg.v16.i31.3897
Figure 1
Figure 1 Immunohistochemical expression of protein S100A4. A: Protein S100A4 expression in normal colorectal epithelium. In all normal colonic epithelium, protein S100A4 immunoreactivity was clearly absent at both cytoplasm and nucleus; B: Negative expression of protein S100A4 in colorectal cancer (CRC); C: Positive expression of protein S100A4 in CRC. Cytoplasm of cancer cells was diffusely stained brown (all at × 200 magnification).
Figure 2
Figure 2 Immunohistochemical expression of E-cadherin. A: E-cadherin expression in normal colorectal epithelium. Normal epithelial cells strongly and homogeneously expressed E-cadherin at intercellular boundaries; B: Preserved expression of E-cadherin in colorectal cancer (CRC); C: Reduced expression of E-cadherin in CRC. Staining of cancer cell at intercellular border was weak and heterogeneous (all at × 200 magnification).
Figure 3
Figure 3 Immunohistochemical expression of p53. A: p53 expression in normal colorectal epithelium. In all normal colonic epithelium, p53 immunoreactivity was clearly absent at nucleus; B: Negative expression of p53 in colorectal cancer (CRC); C: Positive expression of p53 in CRC. More than 10% of cancer cells were stained strongly at their nuclei (all at × 200 magnification).
Figure 4
Figure 4 Kaplan-Meier survival curves demonstrating statistically significant differences according to the expression of protein S100A4 (log-rank test, P = 0. 044). Censored observations are shown as tick marks.