Antitumor effects of novel compound, guttiferone K, on colon cancer by p21Waf1/Cip1-mediated G0/G1 cell cycle arrest and apoptosis
文献类型：期刊论文
| 作者 | Kan, Winnie Lai Ting1; Yin, Chun1; Xu, Hong Xi2; Xu, Gang3 ; To, Kenneth Kin Wah4; Cho, Chi Hin1; Rudd, John Anthony1; Lin, Ge1
|
| 刊名 | INTERNATIONAL JOURNAL OF CANCER
 |
| 出版日期 | 2013-02-01 |
| 卷号 | 132期号:3页码:707-716 |
| 关键词 | guttiferone K anti-tumor colon cancer apoptosis cell cycle |
| ISSN号 | 0020-7136 |
| 通讯作者 | Lin, G (reprint author), Chinese Univ Hong Kong, Sch Biomed Sci, Fac Med, Room 505A,5-F Lo Kwee Seong Integrated Biomed Sci, Shatin, Hong Kong, Peoples R China.，xuhongxi88@gmail.com ; linge@cuhk.edu.hk |
| 英文摘要 | Low selectivity is one of the major problems of currently used anticancer drugs, therefore, there is a high demand for novel, selective antitumor agents. In this study, the anticancer effects and mechanisms of guttiferone K (GUTK), a novel polyprenylated acylphloroglucinol derivative isolated from Garcinia cowa Roxb., were examined for its development as a novel drug targeting colon cancer. GUTK concentration- and time-dependently reduced the viability of human colon cancer HT-29 cells (IC50 value 5.39 +/- 0.22 mu M) without affecting the viability of normal human colon epithelial CCD 841 CoN cells and induced G0/G1 cell cycle arrest in HT-29 cells by down-regulating cyclins D1, D3 and cyclin-dependent kinases 4 and 6, while selectively restoring p21Waf1/Cip1 and p27Kip1 to levels comparable to those observed in normal colon cells, without affecting their levels in normal cells. GUTK (10.0 mu M) induced cleavage of PARP, caspases-3, -8 and -9 and chromatin condensation to stimulate caspase-3-mediated apoptosis. The addition of a JNK inhibitor, SP600125, partially reversed GUTK-induced caspase-3 activity, indicating the possible involvement of JNK in GUTK-induced apoptosis. Furthermore, GUTK (10 mg/kg, i.p.) significantly decreased the tumor volume in a syngeneic colon tumor model when used alone or in combination with 5-fluorouracil without toxicity to the mice. Immunohistochemical staining of the tumor sections revealed a mechanism involving an increase in cleaved caspase-3 and a decrease in cell proliferation marker Ki-67. Our results support GUTK as a promising novel, potent and selective antitumor drug candidate for colon cancer. |
| WOS标题词 | Science & Technology ; Life Sciences & Biomedicine |
| 学科主题 | Oncology |
| 类目[WOS] | Oncology |
| 研究领域[WOS] | Oncology |
| 关键词[WOS] | ACID INHIBITS PROLIFERATION ; GAMBOGIC ACID ; TRANSFERRIN RECEPTOR ; GARCINIA-HANBURYI ; P27 EXPRESSION ; IN-VITRO ; CARCINOMA ; XANTHONES ; PROTEIN ; DEATH |
| 收录类别 | SCI |
| 资助信息 | CUHK Direct Grant from The Chinese University of Hong Kong [2041445]; NSF fund from the National Natural Science Foundation of China [81173485] |
| 语种 | 英语 |
| WOS记录号 | WOS:000311620100028 |
| 公开日期 | 2013-03-18 |
| 源URL | [http://ir.kib.ac.cn/handle/151853/16218]  |
| 专题 | 昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室 |
| 作者单位 | 1.Chinese Univ Hong Kong, Sch Biomed Sci, Fac Med, Shatin, Hong Kong, Peoples R China 2.Shanghai Univ Tradit Chinese Med, Sch Pharm, Shanghai, Peoples R China 3.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming, Peoples R China 4.Chinese Univ Hong Kong, Sch Pharm, Fac Med, Shatin, Hong Kong, Peoples R China |
| 推荐引用方式 GB/T 7714 | Kan, Winnie Lai Ting,Yin, Chun,Xu, Hong Xi,et al. Antitumor effects of novel compound, guttiferone K, on colon cancer by p21Waf1/Cip1-mediated G0/G1 cell cycle arrest and apoptosis[J]. INTERNATIONAL JOURNAL OF CANCER,2013,132(3):707-716. |
| APA | Kan, Winnie Lai Ting.,Yin, Chun.,Xu, Hong Xi.,Xu, Gang.,To, Kenneth Kin Wah.,...&Lin, Ge.(2013).Antitumor effects of novel compound, guttiferone K, on colon cancer by p21Waf1/Cip1-mediated G0/G1 cell cycle arrest and apoptosis.INTERNATIONAL JOURNAL OF CANCER,132(3),707-716. |
| MLA | Kan, Winnie Lai Ting,et al."Antitumor effects of novel compound, guttiferone K, on colon cancer by p21Waf1/Cip1-mediated G0/G1 cell cycle arrest and apoptosis".INTERNATIONAL JOURNAL OF CANCER 132.3(2013):707-716. |
入库方式： OAI收割
来源：昆明植物研究所
浏览0
下载0
收藏0
其他版本
除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。