Brief Article
Copyright ©2014 Baishideng Publishing Group Co.
World J Gastroenterol. May 14, 2014; 20(18): 5505-5510
Published online May 14, 2014. doi: 10.3748/wjg.v20.i18.5505
Figure 1
Figure 1 Morphology of apoptotic cells in gastrointestinal cancer seen under light microscopy. The number of apoptotic cells increased following a 3-d period of As2O3 treatment. Typical apoptotic changes were seen in GIC cells after As2O3 treatment, including cellular shrinkage, cell nucleus fragmentation, chromatin condensation, and the appearance of apoptotic bodies. A: Before As2O3 treatment; B: After As2O3 treatment (HE × 40).
Figure 2
Figure 2 Human gastrointestinal cancer cells were observed by transferase dUTP nick end labelling assay, and identified by brown-stained nuclei. The number of apoptotic cells was counted in order to calculate the apoptotic index. A: Gastric cancer before As2O3 treatment; B: Gastric cancer after As2O3 treatment: C: Colon cancer before As2O3 treatment; D: Colon cancer after As2O3 treatment (× 400).
Figure 3
Figure 3 p53 protein expression in human gastrointestinal cancer cells as indicated by brown-stained nuclei. A: Gastric cancer before As2O3 treatment; B: Gastric cancer after As2O3 treatment; C: Colon cancer before As2O3 treatment; D: Colon cancer after As2O3 treatment (× 400).
Figure 4
Figure 4 Bcl-2 protein expression in human gastrointestinal cancer cells as indicated by brown-stained cytoplasm. A: Gastric cancer before As2O3 treatment; B: Gastric cancer after As2O3 treatment; C: Colon cancer before As2O3 treatment; D: Colon cancer after As2O3 treatment (× 400).
Figure 5
Figure 5 Linear correlation analyses between apoptotic index and Bcl-2 expression in gastric cancer (A) and colon cancer (B) (%). Data are given as mean ± SD. No significant correlation was detected.