Methods: Serum levels of CypB in gastric cancer patients and healthy volunteers were measured by ELISA. The expression patterns of CypB were observed in gastric cancer and adjacent non-tumor tissue using immunohistochemistry. MTT, colony formation and cell cycle assays were used to examine the effects of knock-down CypB on the cell growth, proliferation. DNA aptamers specific to CypB were islolated
by SELEX. Binding affinity (Kd) was determined in direct binding assay by flow cytometry analysis. Results: CypB is over-expressed in both serum and tissues of gastric cancer patients. Knock-down of CypB can inhibit gastric cancer cell Daporinad in vivo growth, proliferation, cell cycle progress and tumorigenesis. Two aptmers which can bind to CypB protein with high affinity and specificity were isolated through SELEX. Conclusion: These findings indiccate CypB could be a potential biomarker and therapeutic target for Ensartinib concentration gastric cancer. CypB-specific aptamers were succusfully isolated, which may be used in further study and future application of CypB. Key Word(s): 1. CypB; 2. gastric cancer; 3. aptamer; 4. SELEX; Presenting
Author: WANG AIYING Additional Authors: ZHU DAN Corresponding Author: WANG AIYING Affiliations: Peking University Third Hospital Objective: This study was to evaluate expression of Bax, Cyt- C and Ki – 67 in DMH induced rat small intestinal and colorectal tumor. Methods: 7 small tumors and 28 colon tumors specimens from 25 male Wistar rats induced by DMH, 9 control only rats, were detected by 上海皓元 Pathology and immunohistochemistry detection. The immunohistochemical detection expression of Bax, Cyt −C and Ki – 67 in the tumor and normal tissue, the statistical processing using chi-square test. Results: (1) the positive expression of Bax in the normal tissue and tumor of small intestine were 88.89% and 14.29% respectively; (2) positive expression of Bax in normal tissue and tumor of colon were 44.44% and 89.29% respectively; (3) Cyt – C positive expression
were 100% and 42.86% in normal small intestine and tumors; (4) Cyt C positive expression were 88.89% and 32.14% respectively in normal colon and tumor; (5) normal intestine without positive expression of Ki – 67, small intestine tumor 71.43% positive expression; (6) positive expression of Ki – 67 was 22.22% in normal colon, and 67.86% in colon cancer. Above all have significant difference between groups (P < 0.05). Conclusion: Cyt-C down regulation and Ki- 67 up regulation may promote the occurrence of small and large intestinan tumor. In the normal small intestinal tissue, the expression of Bax was higher than normal colon tissues, Cyt – C high expression and no expression of Ki – 67, may explains the significant difference in tumor incurrence between small intestine and colon. Key Word(s): 1. intestinal tumor; 2. Bax; 3. Cyt-C; 4.