Cordycepin inhibits pancreatic cancer cell growth in vitro and in vivo via targeting FGFR2 and blocking ERK signaling
文献类型:期刊论文
作者 | Li Xue-Ying1,3,4; Tao Hong1,3; Jin Can1,3; Du Zhen-Yun1,3; Liao Wen-Feng1,3; Tang Qing-Jiu2; Ding Kan1,3 |
刊名 | CHINESE JOURNAL OF NATURAL MEDICINES |
出版日期 | 2020-04-01 |
卷号 | 18期号:5页码:345-355 |
ISSN号 | 2095-6975 |
关键词 | Cordycepin FGFR2 Apoptosis Pancreatic cancer Ras/Erk |
DOI | 10.1016/S1875-5364(20)30041-8 |
通讯作者 | Tang Qing-Jiu() ; Ding Kan(dingkan@simm.ac.cn) |
英文摘要 | Cordycepin (3'-deoxyadenosine) from Cordyceps militaris has been reported to have anti-tumor effects. However, the molecular target and mechanism underlying cordycepin impeding pancreatic cancer cell growth in vitro and in vivo remain vague. In this study, we reported functional target molecule of cordycepin which inhibited pancreatic cancer cells growth in vitro and in vivo. Cordycepin was confirmed to induce apoptosis by activating caspase-3, caspase-9 and cytochrome c. Further studies suggested that MAPK pathway was blocked by cordycepin via inhibiting the expression of Ras and the phosphorylation of Erk. Moreover, cordycepin caused S-phase arrest and DNA damage associated with activating Chk2 (checkpoint kinase 2) pathway and downregulating cyclin A2 and CDK2 phosphorylation. Very interestingly, we showed that cordycepin could bind to FGFR2 (K-D = 7.77 x 10(-9)) very potently to inhibit pancreatic cancer cells growth by blocking Ras/ErK pathway. These results suggest that cordycepin could potentially be a leading compound which targeted FGFR2 to inhibit pancreatic cells growth by inducing cell apoptosis and causing cell cycle arrest via blocking FGFR/Ras/ERK signaling for anti-pancreatic cancer new drug development. |
WOS关键词 | CYTOCHROME-C RELEASE ; INDUCED APOPTOSIS ; PROTEIN ; ACTIVATION ; PATHWAY ; STATISTICS ; GENE ; BAX |
资助项目 | Strategic Priority Research Program of the Chinese Academy of Sciences[XDA12010302] ; National Natural Science Foundation of China[31230022] ; Program of Shanghai Subject Chief Scientist[16XD1404500] |
WOS研究方向 | Integrative & Complementary Medicine ; Pharmacology & Pharmacy |
语种 | 英语 |
出版者 | CHINESE JOURNAL NATURAL MEDICINES |
WOS记录号 | WOS:000536286200002 |
源URL | [http://119.78.100.183/handle/2S10ELR8/280098] |
专题 | 中国科学院上海药物研究所 |
通讯作者 | Tang Qing-Jiu; Ding Kan |
作者单位 | 1.Univ Chinese Acad Sci, Beijing 100049, Peoples R China 2.Shanghai Acad Agr Sci, Inst Edible Fungi, Shanghai 201203, Peoples R China 3.Chinese Acad Sci, Glycochemistry & Glycobiol Lab, Key Lab Receptor Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 4.Nanchang Univ, Coll Pharm, Nanchang 330006, Jiangxi, Peoples R China |
推荐引用方式 GB/T 7714 | Li Xue-Ying,Tao Hong,Jin Can,et al. Cordycepin inhibits pancreatic cancer cell growth in vitro and in vivo via targeting FGFR2 and blocking ERK signaling[J]. CHINESE JOURNAL OF NATURAL MEDICINES,2020,18(5):345-355. |
APA | Li Xue-Ying.,Tao Hong.,Jin Can.,Du Zhen-Yun.,Liao Wen-Feng.,...&Ding Kan.(2020).Cordycepin inhibits pancreatic cancer cell growth in vitro and in vivo via targeting FGFR2 and blocking ERK signaling.CHINESE JOURNAL OF NATURAL MEDICINES,18(5),345-355. |
MLA | Li Xue-Ying,et al."Cordycepin inhibits pancreatic cancer cell growth in vitro and in vivo via targeting FGFR2 and blocking ERK signaling".CHINESE JOURNAL OF NATURAL MEDICINES 18.5(2020):345-355. |
入库方式: OAI收割
来源:上海药物研究所
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