标题:Inhibition of angiogenesis and invasion by DMBT is mediated by downregulation of VEGF and MMP-9 through Akt pathway in MDA-MB-231 breast cancer cells
作者:Tang, Linlin; Ma, Xiaowen; Tian, Qi; Cheng, Yanna; Yao, Hong; Liu, Zhaopeng; Qu, Xianjun; Han, Xiuzhen
作者机构:[Tang, Linlin; Ma, Xiaowen; Tian, Qi; Cheng, Yanna; Yao, Hong; Qu, Xianjun; Han, Xiuzhen] Shandong Univ, Sch Pharmaceut Sci, Dept Pharmacol, Jinan 250 更多
通讯作者:Han, XZ
通讯作者地址:[Han, XZ]Shandong Univ, Sch Pharmaceut Sci, Dept Pharmacol, 44 West Wenhua Rd, Jinan 250012, Peoples R China.
来源:FOOD AND CHEMICAL TOXICOLOGY
出版年:2013
卷:56
页码:204-213
DOI:10.1016/j.fct.2013.02.032
关键词:Trehalose derivatives; DMBT; VEGF; MMP-9; Akt
摘要:Invasion, either directly or via metastasis formation, is the main cause of death in cancer patients, development of efficient anti-invasive agents is an important research challenge. In order to obtain more potent inhibitors, a series of brartemicin analogs were synthesized and evaluated for their inhibitory activity against invasion. Among the synthetic analogs tested, DMBT, 6,6'-bis (2,3-dimethoxybenzoyl)-a,a-n-trehalose, was found to be the most potent anti-invasive agent. But the effects of DMBT on breast cancer cells were not known. In this study, the effects of DMBT on invasion and metastasis in MDA-MB-231 cells were investigated. MTT assay showed that no obvious inhibitory or cytotoxic effect of DMBT was found. DMBT could inhibit invasion, migration and tube formation of HUVECs. Gelatin zymography showed that DMBT inhibited secretion and activity of MMP-9. Western blotting demonstrated that DMBT effectively suppressed the expression of VEGF, p-VEGFR-2, p-EGFR, and p-Akt. These results suggested that DMBT could inhibit invasion and angiogenesis by downregulation of VEGF and MMP-9, resulting from the inhibition of Akt pathway. DMBT might be a promising lead molecule for the anti-metastasis and serve as a therapeutic agent to inhibit breast cancer cell invasion and metastasis. (C) 2013 Elsevier Ltd. All rights reserved.
收录类别:SCOPUS;SCIE
WOS核心被引频次:21
Scopus被引频次:22
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84875359127&doi=10.1016%2fj.fct.2013.02.032&partnerID=40&md5=ac3687c45254b491b81c5a8b0718e44b
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