diphenyl difluoroketone a potent chemotherapy candidate for human hepatocellular carcinoma二苯difluoroketone人类肝细胞癌化疗一个强有力的候选人.pdfVIP

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diphenyl difluoroketone a potent chemotherapy candidate for human hepatocellular carcinoma二苯difluoroketone人类肝细胞癌化疗一个强有力的候选人.pdf

diphenyl difluoroketone a potent chemotherapy candidate for human hepatocellular carcinoma二苯difluoroketone人类肝细胞癌化疗一个强有力的候选人

Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma 1. 1. 2 1 1 1 Yingjian Liang , Dalong Yin , Limin Hou , Tongsen Zheng , Jiabei Wang , Xianzhi Meng , Zhaoyang 1 1 1 1 1 Lu , Xuan Song , Shangha Pan , Hongchi Jiang , Lianxin Liu * 1 Key Laboratory of Hepatosplenic Surgery, Department of General Surgery, The First Affiliated Hospital of Harbin Medical University, Ministry of Education, Harbin, Heilongjiang Province, People’s Republic of China, 2 Department of Emergency Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, People’s Republic of China Abstract Diphenyl difluoroketone (EF24), a molecule having structural similarity to curcumin, was recently reported to inhibit proliferation of various cancer cells significantly. Here we try to determine the effect and mechanism of EF24 on hepatocellular carcinoma. 2 mM EF24 was found to inhibit the proliferation of PLC/PRF/5, Hep3B, HepG2, SK-HEP-1 and Huh 7 cell lines. However, even 8 mM EF24 treatment did not affect the proliferation of normal liver LO2 cells. Accordingly, 20 mg/kg/d EF24 inhibited the growth of the tumor xenografts conspicuously while causing no apparent change in liver, spleen or body weight. In addition, significant apoptosis and G2/M phase cell cycle arrest were found using flow cytometry. Besides, caspases and PARP activation and features typical of apoptosis including fragmented nuclei with condensed chromatin were also observed. Furthermore, the mechanism was targeted at the reducti

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