Angiopoietin-like 4 enhances metastasis and inhibits apoptosis via inducing bone morphogenetic protein 7 in colorectal cancer cells

被引:29
|
作者
Li, Xuquan
Chen, Tao
Shi, Qiang
Li, Jian
Cai, Shilun
Zhou, Pinghong
Zhong, Yunshi
Yao, Liqing
机构
[1] Fudan Univ, Zhongshan Hosp, Endoscopy Ctr, Shanghai 200032, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Endoscopy Res Inst, Shanghai 200032, Peoples R China
基金
美国国家科学基金会;
关键词
ANGPTL4; BMP7; Metastasis; Apoptosis; Colorectal cancer; HEPATOCELLULAR-CARCINOMA; VASCULAR-PERMEABILITY; COLON-CANCER; EXPRESSION; ANGPTL4; INVASION; BMP7; ANGIOGENESIS; MIGRATION; INTERACTS;
D O I
10.1016/j.bbrc.2015.09.104
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiopoietin-like 4 (ANGPTL4), a secretory glycoprotein, plays an important role in cancer metastasis. In the present study, we aim to investigate the roles and mechanisms of ANGPTL4 in the regulation of colorectal cancer metastasis. We found that expression level of ANGPTL4 was increased in colorectal cancer tissues, compared with that in normal tissues. Moreover, liver metastasis was significantly associated with higher expression of ANGPTL4. In vitro studies further showed that overexpression of ANGPTL4 enhanced cell migration, invasion and inhibited apoptosis. At the molecular level, ANGPTL4 overexpression resulted in an up-regulation of bone morphogenetic protein 7 (BMP7). Indeed, knockdown of BMP7 by small interfering RNA (siRNA) oligos reversed the roles of ANGPTL4 overexpression in HCT116 cells. Finally, in vivo studies further confirmed the metastatic roles of ANGPTL4 by inducing BMP7. Therefore, our study demonstrated that ANGPTL4 might promote metastasis and might inhibit apoptosis of colorectal cancer cells by up-regulation of BMP7. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:128 / 134
页数:7
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