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논문 기본 정보

자료유형
학술저널
저자정보
Tu, Bo (Department of Ultrasonic Medicine, The First Affiliated Hospital of Chongqing Medical University) Ma, Ting-Ting (Key Laboratory of Laboratory Medical Diagnostics of Education Ministry, Chongqing Medical University) Peng, Xiao-Qiong (Department of Ultrasonic Medicine, The First Affiliated Hospital of Chongqing Medical University) Wang, Qin (Key Laboratory of Laboratory Medical Diagnostics of Education Ministry, Chongqing Medical University) Yang, Hong (Department of Ultrasonic Medicine, The First Affiliated Hospital of Chongqing Medical University) Huang, Xiao-Ling (Department of Ultrasonic Medicine, The First Affiliated Hospital of Chongqing Medical University)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제15권 제20호
발행연도
2014.1
수록면
8,829 - 8,836 (8page)

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Background: Cyclooxygenase-2 (COX-2), considered to have tumor-promoting potential, is highly expressed in a variety of tumors, including breast cancer. Since the functions and action mechanisms of COX-2 in breast cancer have not been fully elucidated, in the present study, the effects of target inhibiting COX-2 with recombinant adenovirus Ad-COX-2-shRNA on malignant biological behavior were investigated in representative cell lines. Materials and Methods: Breast cancer MDA-MB-231 and MCF-7 cells were transfected with Ad-COX-2-shRNA and COX-2 expression was tested by RT-PCR and Western blotting. Changes in proliferation, apoptosis and invasion of breast cancer cells were detected with various assays including MTT, colony forming, flowcytometry and Transwell invasion tests. The expression of related proteins involved in the cell cycle, apoptosis, invasion and signaling pathways was assessed by Western blotting. Results: COX-2 expression was significantly reduced in both breast cancer cell lines infected with Ad-COX-2-shRNA, with obvious inhibition of proliferation, colony forming rate, G2/M phase passage and invasion, as well as induction of apoptosis, in MDA-MB-231 and MCF-7 cells, respectively. At the same time, proteins related to the cell cycle, anti-apoptosis and invasion were significantly downregulated. In addition, c-myc expression and phosphorylation activation of Wnt/${\beta}$-catenin and p38MAPK pathways were reduced by the Ad-COX-2-shRNA. Conclusions: COX-2 expression is associated with proliferation, apoptosis and invasion of breast cancer cells, and its mechanisms of action involve regulating expression of c-myc through the p38MAPK and Wnt/${\beta}$-catenin pathways.

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