Kuo Po-Lin, Hsu Ya-Ling, Sung Shu-Chiao, Ni Wen-Chiu, Lin Ta-Chen, Lin Chun-Ching
Department of Biotechnology, Cell Biology Laboratory, Institute of Cosmetic Science, Chia-Nan University of Pharmacy and Science, Tainan, Taiwan, ROC.
Anticancer Drugs. 2007 Jun;18(5):555-62. doi: 10.1097/CAD.0b013e3280262437.
Pterocarnin A, isolated from the bark of Pterocarya stenoptera (Juylandaceae), was investigated for its antiproliferative activity in human breast adenocarcinoma MCF-7 cells. To identify the anticancer mechanism of pterocarnin A, we assayed its effects on apoptosis, cell cycle distribution, and levels of p53, p21/WAF1, Fas/APO-1 receptor and Fas ligand. The results showed that pterocarnin A induced apoptosis of MCF-7 cells without mediation of p53 and p21/WAF1. We suggest that the Fas/Fas ligand apoptotic system is the main pathway of pterocarnin A-mediated apoptosis of MCF-7 cells. Our study reports here for the first time that the activity of the Fas/Fas ligand apoptotic system may participate in the antiproliferative activity of pterocarnin A in MCF-7 cells.
从枫杨(胡桃科)树皮中分离得到的翼皮花椒素A,对其在人乳腺腺癌MCF-7细胞中的抗增殖活性进行了研究。为确定翼皮花椒素A的抗癌机制,我们检测了其对细胞凋亡、细胞周期分布以及p53、p21/WAF1、Fas/APO-1受体和Fas配体水平的影响。结果表明,翼皮花椒素A可诱导MCF-7细胞凋亡,且不依赖p53和p21/WAF1的介导。我们认为Fas/Fas配体凋亡系统是翼皮花椒素A介导MCF-7细胞凋亡的主要途径。我们的研究首次报道,Fas/Fas配体凋亡系统的活性可能参与了翼皮花椒素A对MCF-7细胞的抗增殖活性。