Cargando…
Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma
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 µM EF24 was found to inhibit the prolife...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162018/ https://www.ncbi.nlm.nih.gov/pubmed/21901145 http://dx.doi.org/10.1371/journal.pone.0023908 |
_version_ | 1782210780052062208 |
---|---|
author | Liang, Yingjian Yin, Dalong Hou, Limin Zheng, Tongsen Wang, Jiabei Meng, Xianzhi Lu, Zhaoyang Song, Xuan Pan, Shangha Jiang, Hongchi Liu, Lianxin |
author_facet | Liang, Yingjian Yin, Dalong Hou, Limin Zheng, Tongsen Wang, Jiabei Meng, Xianzhi Lu, Zhaoyang Song, Xuan Pan, Shangha Jiang, Hongchi Liu, Lianxin |
author_sort | Liang, Yingjian |
collection | PubMed |
description | 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 µM EF24 was found to inhibit the proliferation of PLC/PRF/5, Hep3B, HepG2, SK-HEP-1 and Huh 7 cell lines. However, even 8 µM 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-κB) pathway and the NF-κB–regulated gene products Bcl-2, COX-2, Cyclin B1. Our study has offered a strategy that EF24 being a therapeutic agent for hepatocellular carcinoma. |
format | Online Article Text |
id | pubmed-3162018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31620182011-09-07 Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma Liang, Yingjian Yin, Dalong Hou, Limin Zheng, Tongsen Wang, Jiabei Meng, Xianzhi Lu, Zhaoyang Song, Xuan Pan, Shangha Jiang, Hongchi Liu, Lianxin PLoS One Research Article 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 µM EF24 was found to inhibit the proliferation of PLC/PRF/5, Hep3B, HepG2, SK-HEP-1 and Huh 7 cell lines. However, even 8 µM 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-κB) pathway and the NF-κB–regulated gene products Bcl-2, COX-2, Cyclin B1. Our study has offered a strategy that EF24 being a therapeutic agent for hepatocellular carcinoma. Public Library of Science 2011-08-25 /pmc/articles/PMC3162018/ /pubmed/21901145 http://dx.doi.org/10.1371/journal.pone.0023908 Text en Liang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Liang, Yingjian Yin, Dalong Hou, Limin Zheng, Tongsen Wang, Jiabei Meng, Xianzhi Lu, Zhaoyang Song, Xuan Pan, Shangha Jiang, Hongchi Liu, Lianxin Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title | Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title_full | Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title_fullStr | Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title_full_unstemmed | Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title_short | Diphenyl Difluoroketone: A Potent Chemotherapy Candidate for Human Hepatocellular Carcinoma |
title_sort | diphenyl difluoroketone: a potent chemotherapy candidate for human hepatocellular carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162018/ https://www.ncbi.nlm.nih.gov/pubmed/21901145 http://dx.doi.org/10.1371/journal.pone.0023908 |
work_keys_str_mv | AT liangyingjian diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT yindalong diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT houlimin diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT zhengtongsen diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT wangjiabei diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT mengxianzhi diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT luzhaoyang diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT songxuan diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT panshangha diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT jianghongchi diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma AT liulianxin diphenyldifluoroketoneapotentchemotherapycandidateforhumanhepatocellularcarcinoma |