Interaction of Ganoderma triterpenes with doxorubicin and proteomic characterization of the possible molecular targets of Ganoderma triterpenes
Yue, Qing-Xi; Xie, Fu-Bo; Guan, Shu-Hong; Ma, Chao; Yang, Min; Jiang, Bao-Hong; Liu, Xuan; Guo, De-An
刊名CANCER SCIENCE
2008-07
卷号99期号:7页码:1461-1470
ISSN号1347-9032
DOI10.1111/j.1349-7006.2008.00824.x
文献子类Article
英文摘要Triterpenes are the main components with cytotoxicity in Ganoderma lucidum, which is used popularly as a complementary treatment for cancer therapy in traditional Chinese medicine. To investigate the possible interaction between chemotherapeutic agents and triterpenes extracted from G. lucidum, the cytotoxicity of doxorubicin (DOX) combined with Ganoderma triterpenes (GTS) or lucidenic acid N (LCN), a purified compound, was examined in HeLa cells. The combinations targeting DOX with GTS or LCN resulted in a synergistic interaction in HeLa cells. Moreover, to identify the molecular targets of GTS, two-dimensional gel electrophoresis-based comparative proteomics was carried out and proteins with altered expression levels after GTS treatment in HeLa cells were identified by matrix-assisted laser desorption/ionization time-of-flight tandem mass spectrometry. The results of our proteomic study indicated that the GTS treatment caused regulated expression of 14 proteins, which play important roles in cell proliferation, the cell cycle, apoptosis, and oxidative stress. Flow cytometric analysis confirmed that GTS could induce weak G(0) - G(1) phase arrest and combined use of GTS with DOX could induce apoptosis in cells. Furthermore, GTS enhanced the reactive oxygen species (ROS)-producing effect of DOX, and a ROS scavenger could affect the synergism between GTS and DOX. In cells with high Ku80 protein expression, the synergism between GTS and DOX was also partly affected. Importantly, in cells with high Ku80 expression that were treated with a ROS scavenger, the synergism between GTS and DOX totally disappeared. These results suggest that the synergism between GTS and DOX might be based on GTS-induced sensitization of cells to chemotherapeutics through enhanced oxidative stress, DNA damage, and apoptosis.
WOS关键词PROSTATE-CANCER CELLS ; OXIDATIVE STRESS ; CYCLE ARREST ; INHIBITS PROLIFERATION ; COLORECTAL-CANCER ; IN-VITRO ; LUCIDUM ; PROTEIN ; APOPTOSIS ; GROWTH
WOS研究方向Oncology
语种英语
出版者WILEY-BLACKWELL
WOS记录号WOS:000256351900024
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/272873]  
专题上海中药现代化研究中心
通讯作者Liu, Xuan
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai Res Ctr Modernizat Tradit Chinese Med, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Yue, Qing-Xi,Xie, Fu-Bo,Guan, Shu-Hong,et al. Interaction of Ganoderma triterpenes with doxorubicin and proteomic characterization of the possible molecular targets of Ganoderma triterpenes[J]. CANCER SCIENCE,2008,99(7):1461-1470.
APA Yue, Qing-Xi.,Xie, Fu-Bo.,Guan, Shu-Hong.,Ma, Chao.,Yang, Min.,...&Guo, De-An.(2008).Interaction of Ganoderma triterpenes with doxorubicin and proteomic characterization of the possible molecular targets of Ganoderma triterpenes.CANCER SCIENCE,99(7),1461-1470.
MLA Yue, Qing-Xi,et al."Interaction of Ganoderma triterpenes with doxorubicin and proteomic characterization of the possible molecular targets of Ganoderma triterpenes".CANCER SCIENCE 99.7(2008):1461-1470.
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