Residential College | false |
Status | 已發表Published |
Furanodiene induces G2/M cell cycle arrest and apoptosis through MAPK signaling and mitochondria-caspase pathway in human hepatocellular carcinoma cells | |
Xiao,Yu1,2; Yang,Feng Qing1; Li,Shao Ping1; Gao,Jian Li1; Hu,Guang1; Lao,Sin Cheng1; Conceição,Emilia Leong1; Fung,Kwok Pui3,4; Wang,Yi Tao1,5; Lee,Simon Ming Yuen1,4 | |
2007 | |
Source Publication | Cancer Biology and Therapy |
ISSN | 1538-4047 |
Volume | 6Issue:7Pages:1044-1050 |
Abstract | Furanodiene (CHO), a pure compound isolated from Traditional Chinese medicine, Curcuma wenyujin, named Ezhu in Chinese, which structure was determined on the basis of NMR, MS and UV spectrum. In this study, we attempted to characterize in detail the signaling cascades resulted from furanodiene-induced apoptosis in human hepatoma HepG2 cells. Furanodiene inhibited HepG2 cell growth by causing cell cycle arrest at G/M and inducing apoptosis as evidenced by DNA fragmentation assay. We found that furanodiene induced mitochondrial transmembrane depolarization, release of mitochondrial cytochrome c, activation of caspases-3 and the cleavage of PARP. The furanodiene mediated mitochondria-caspase apoptotic pathway also involved activation of p38 and inhibition of ERK mitogen-activated protein kinase (MAPK) signaling. These results for the first time have identified the biological activity of furanodiene against HepG2 cells and provide rationales for further development of essential oil of Ezhu and its ingredients such as furanodiene on treatment of liver diseases. ©2007 Landes Bioscience. |
Keyword | Apoptosis Caspase-3 Cytochrome c Erk Furanodiene Hepg2 Mitochondrial P38 |
DOI | 10.4161/cbt.6.7.4317 |
URL | View the original |
Indexed By | SCIE |
Language | 英語English |
WOS Research Area | Oncology |
WOS Subject | Oncology |
WOS ID | WOS:000250805900020 |
Scopus ID | 2-s2.0-42449136597 |
Fulltext Access | |
Citation statistics | |
Document Type | Journal article |
Collection | DEPARTMENT OF PHARMACEUTICAL SCIENCES Institute of Chinese Medical Sciences |
Corresponding Author | Lee,Simon Ming Yuen |
Affiliation | 1.Institute of Chinese Medical Sciences,University of Macau,Taipa,Macao 2.Science and Technology Department,Sichuan Provincial People's Hospital,Sichuan Academy of Medical Science,Chengdu,China 3.Department of Biochemistry,Chinese University of Hong Kong,Hong Kong,Hong Kong 4.Institute of Chinese Medical,Chinese University of Hong Kong,Hong Kong,Hong Kong 5.Institute of Chinese Medicine Sciences,University of Macau,Taipa,Macao |
First Author Affilication | Institute of Chinese Medical Sciences |
Corresponding Author Affilication | Institute of Chinese Medical Sciences |
Recommended Citation GB/T 7714 | Xiao,Yu,Yang,Feng Qing,Li,Shao Ping,et al. Furanodiene induces G2/M cell cycle arrest and apoptosis through MAPK signaling and mitochondria-caspase pathway in human hepatocellular carcinoma cells[J]. Cancer Biology and Therapy, 2007, 6(7), 1044-1050. |
APA | Xiao,Yu., Yang,Feng Qing., Li,Shao Ping., Gao,Jian Li., Hu,Guang., Lao,Sin Cheng., Conceição,Emilia Leong., Fung,Kwok Pui., Wang,Yi Tao., & Lee,Simon Ming Yuen (2007). Furanodiene induces G2/M cell cycle arrest and apoptosis through MAPK signaling and mitochondria-caspase pathway in human hepatocellular carcinoma cells. Cancer Biology and Therapy, 6(7), 1044-1050. |
MLA | Xiao,Yu,et al."Furanodiene induces G2/M cell cycle arrest and apoptosis through MAPK signaling and mitochondria-caspase pathway in human hepatocellular carcinoma cells".Cancer Biology and Therapy 6.7(2007):1044-1050. |
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