K604, a specific acyl-CoA:cholesterol acyltransferase 1 inhibitor, suppresses proliferation of U251-MG glioblastoma Cells

被引:30
作者
Ohmoto, Takuji [1 ]
Nishitsuji, Kazuchika [1 ]
Yoshitani, Nobuyuki [1 ]
Mizuguchi, Makoto [1 ]
Yanagisawa, Yuto [2 ,3 ]
Saito, Hiroyuki [2 ,3 ]
Sakashita, Naomi [1 ]
机构
[1] Univ Tokushima, Grad Sch, Inst Hlth Biosci, Dept Human Pathol, Tokushima 7708503, Japan
[2] Univ Tokushima, Inst Hlth Biosci, Dept Phys Pharmaceut, Tokushima 7708505, Japan
[3] Univ Tokushima, Grad Sch Pharmaceut Sci, Tokushima 7708505, Japan
基金
日本学术振兴会;
关键词
acyl-CoA:cholesterol acyltransferase 1; glioblastoma; acyl-CoA:cholesterol acyltransferase inhibitor; cell proliferation; cholesteryl ester; A-CHOLESTEROL ACYLTRANSFERASE; LIPID RAFTS; COENZYME; ACTIVATION; SURVIVAL; GLIOMA; CD44; KINASE; PALMITOYLATION; MIGRATION;
D O I
10.3892/mmr.2015.4200
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma is the most aggressive type of brain tumor and has a poor prognosis. Increased levels of cholesteryl ester and simultaneous expression of acyl-CoA:cholesterol acyltransferase 1 (ACAT1) in tumor cells indicated that cholesterol esterification is critical to tumor growth. The present study confirmed that human glioblastoma tissues as well as the glioblastoma cell line U251-MG showed significant expression of ACAT1. ACAT1 expression in U251-MG cells increased in a cell proliferation-dependent manner. K604, a selective ACAT1 inhibitor, suppressed the proliferation of U251-MG cells and downregulated the activation of Akt and extracellular signal-regulated kinase in proliferating glioblastoma cells. These results suggested that ACAT1 may be a therapeutic target for the treatment of glioblastoma, with K604 as an effective therapeutic agent.
引用
收藏
页码:6037 / 6042
页数:6
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