咖啡因
结直肠癌
转移
绿原酸
癌症
肿瘤转化
癌症研究
磷酸化
医学
MAPK/ERK通路
咖啡酸
药理学
生物化学
内科学
化学
癌变
食品科学
抗氧化剂
作者
Nam Joo Kang,Ki Won Lee,Bo Hyun Kim,Ann M. Bode,Hyo‐Jeong Lee,Yong-Seok Heo,Lisa A. Boardman,Paul J. Limburg,Hyong Joo Lee,Zigang Dong
出处
期刊:Carcinogenesis
[Oxford University Press]
日期:2011-02-11
卷期号:32 (6): 921-928
被引量:119
标识
DOI:10.1093/carcin/bgr022
摘要
Epidemiological studies suggest that coffee consumption reduces the risk of cancers, including colon cancer, but the molecular mechanisms and target(s) underlying the chemopreventive effects of coffee and its active ingredient(s) remain unknown. Based on serving size or daily units, coffee contains larger amounts of phenolic phytochemicals than tea or red wine. Coffee or chlorogenic acid inhibited CT-26 colon cancer cell-induced lung metastasis by blocking phosphorylation of ERKs. Coffee or caffeic acid (CaA) strongly suppressed mitogen-activated MEK1 and TOPK activities and bound directly to either MEK1 or TOPK in an ATP-noncompetitive manner. Coffee or CaA, but not caffeine, inhibited ERKs phosphorylation, AP-1 and NF-κB transactivation and subsequently inhibited TPA-, EGF- and H-Ras-induced neoplastic transformation of JB6 P+ cells. Coffee consumption was also associated with a significant attenuation of ERKs phosphorylation in colon cancer patients. These results suggest that coffee and CaA target MEK1 and TOPK to suppress colon cancer metastasis and neoplastic cell transformation.
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