Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma

被引:28
作者
Liang, Yingjian [1 ]
Yin, Dalong [1 ]
Hou, Limin [2 ]
Zheng, Tongsen [1 ]
Wang, Jiabei [1 ]
Meng, Xianzhi [1 ]
Lu, Zhaoyang [1 ]
Song, Xuan [1 ]
Pan, Shangha [1 ]
Jiang, Hongchi [1 ]
Liu, Lianxin [1 ]
机构
[1] Harbin Med Coll, Key Lab Hepatosplen Surg, Dept Gen Surg, Minist Educ,Affiliated Hosp 1, Harbin, Heilongjiang Pr, Peoples R China
[2] Harbin Med Coll, Dept Emergency Surg, Affiliated Hosp 1, Harbin, Heilongjiang Pr, Peoples R China
关键词
HEPATOMA G2 CELLS; FACTOR-KAPPA-B; ANTICANCER ACTIVITY; CURCUMIN ANALOGS; CANCER-CELLS; APOPTOSIS; EF24; ANGIOGENESIS; DOXORUBICIN; RECEPTOR;
D O I
10.1371/journal.pone.0023908
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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 mu M EF24 was found to inhibit the proliferation of PLC/PRF/5, Hep3B, HepG2, SK-HEP-1 and Huh 7 cell lines. However, even 8 mu M 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 G(2)/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 reduction of nuclear factor kappa b (NF-kappa kB) pathway and the NF-kappa B-regulated gene products Bcl-2, COX-2, Cyclin B1. Our study has offered a strategy that EF24 being a therapeutic agent for hepatocellular carcinoma.
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页数:9
相关论文
共 40 条
[1]
EF24, a novel synthetic curcumin analog, induces apoptosis in cancer cells via a redox-dependent mechanism [J].
Adams, BK ;
Cai, JY ;
Armstrong, J ;
Herold, M ;
Lu, YJ ;
Sum, AM ;
Snyder, JR ;
Liotta, DC ;
Jones, DR ;
Shoji, M .
ANTI-CANCER DRUGS, 2005, 16 (03) :263-275
[2]
Synthesis and biological evaluation of novel curcumin analogs as anti-cancer and anti-angiogenesis agents [J].
Adams, BK ;
Ferstl, EM ;
Davis, MC ;
Herold, M ;
Kurtkaya, S ;
Camalier, RF ;
Hollingshead, MG ;
Kaur, G ;
Sausville, EA ;
Rickles, FR ;
Snyder, JP ;
Liotta, DC ;
Shoji, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (14) :3871-3883
[3]
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[4]
Curcumin and cancer: An "old-age" disease with an "age-old" solution [J].
Anand, Preetha ;
Sundaram, Chitra ;
Jhurani, Sonia ;
Kunnumakkara, Ajaikumar B. ;
Aggarwal, Bharat B. .
CANCER LETTERS, 2008, 267 (01) :133-164
[5]
[Anonymous], 1995, N ENGL J MED, V332, P1256
[6]
Antoon J.W., 2011, CANC BIOL THER, V11
[7]
Bae MK, 2006, ONCOL REP, V15, P1557
[8]
Bruix J, 1997, HEPATOLOGY, V25, P259
[9]
Curcurnin induces apoptosis through mitochondrial hyperpolarization and mtDNA damage in human hepatoma G2 cells [J].
Cao, Jun ;
Liu, Yong ;
Jia, Li ;
Zhou, Hui-Min ;
Kong, Ying ;
Yang, Guang ;
Jiang, Li-Ping ;
Li, Qiu-Juan ;
Zhong, Lai-Fu .
FREE RADICAL BIOLOGY AND MEDICINE, 2007, 43 (06) :968-975
[10]
Mitochondrial and nuclear DNA damage induced by curcumin in human hepatoma G2 cells [J].
Cao, Jun ;
Jia, Li ;
Zhou, Hui-Min ;
Liu, Yong ;
Zhong, Lai-Fu .
TOXICOLOGICAL SCIENCES, 2006, 91 (02) :476-483