标题:Acetyl-11-keto-β-boswellic acid (AKBA) inhibits human gastric carcinoma growth through modulation of the Wnt/β-catenin signaling pathway
作者:Zhang,Y.-S.;Xie,J.-Z.;Zhong,J.-L.;Li,Y.-Y.;Wang,R.-Q.;Qin,Y.-Z.;Lou,H.-X.;Gao,Z.-H.;Qu,X.-J.
作者机构:[Zhang, Y.-S] Department of Pharmacology, School of Pharmaceutical Sciences, Shandong University, Jinan, China;[ Xie, J.-Z] Shandong Center for Drug E 更多
通讯作者:Gao, ZH
通讯作者地址:[Gao, ZH]McGill Univ, Dept Pathol, Montreal, PQ, Canada.
来源:Biochimica et Biophysica Acta. General Subjects
出版年:2013
卷:1830
期:6
页码:3604-3615
DOI:10.1016/j.bbagen.2013.03.003
关键词:Acetyl-11-keto-β-boswellic acid (AKBA);Apoptosis;Gastric carcinoma;Inhibitory effect;Wnt/β-catenin
摘要:Background Acetyl-11-keto-beta-boswellic acid (AKBA) is a derivative of boswellic acid, an active component of Boswellia serrata gum resin. We examined the effect of AKBA on human gastric carcinoma growth and explored the underlying molecular mechanisms. Methods Inhibition of cancer cell growth was estimated by colorimetric and clonogenic assays. Cell cycle distribution was analyzed by flow cytometry and apoptosis determined using Annexin V-FITC/PI staining and DNA ladder quantification. After three weeks of oral AKBA administration in nude mice bearing cancer xenografts, animals were sacrificed and xenografts removed for TUNEL staining and western blot analysis. Results AKBA exhibited anti-cancer activity in vitro and in vivo. With oral application in mice, AKBA significantly inhibited SGC-7901 and MKN-45 xenografts without toxicity. This effect might be associated with its roles in cell cycle arrest and apoptosis induction. The results also showed activation of p21Waf1/Cip1 and p53 in mitochondria and increased cleaved caspase-9, caspase-3, and PARP and Bax/Bcl-2 ratio after AKBA treatment. Further analysis suggested that these effects might arise from AKBA\'s modulation of the aberrant Wnt/β-catenin signaling pathway. Upon AKBA treatment, β-catenin expression in nuclei was inhibited, and membrane β-catenin was activated. In the same sample, active GSK3β was increased and its non-active form decreased. Levels of cyclin D1, PCNA, survivin, c-Myc, MMP-2, and MMP-7, downstream targets of Wnt/β-catenin, were inhibited. Conclusions AKBA effects on human gastric carcinoma growth were associated with its activity in modulating the Wnt/β-catenin signaling pathway. General significance AKBA could be useful in the treatment of gastric cancers.
收录类别:SCOPUS;SCIE
WOS核心被引频次:16
Scopus被引频次:16
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84876008661&doi=10.1016%2fj.bbagen.2013.03.003&partnerID=40&md5=a4b7167577462ff9245110e06a36f3ab
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