MACC-1 Promotes Endothelium-Dependent Angiogenesis in Gastric Cancer by Activating TWIST1/VEGF-A Signal Pathway

被引:43
作者
Wang, Lin [1 ]
Zhou, Rui [1 ]
Zhao, Yang [1 ]
Dong, Shaoting [1 ]
Zhang, Jingwen [1 ]
Luo, Yuhao [1 ]
Huang, Na [1 ]
Shi, Min [1 ]
Bin, Jianping [2 ]
Liao, Yulin [2 ]
Liao, Wangjun [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Oncol, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Cardiol, Guangzhou, Guangdong, Peoples R China
来源
PLOS ONE | 2016年 / 11卷 / 06期
基金
中国国家自然科学基金;
关键词
GROWTH-FACTOR; TUMOR ANGIOGENESIS; VASCULOGENIC MIMICRY; VEGF-A; MESENCHYMAL TRANSITION; BREAST-CANCER; IN-VIVO; METASTASIS; EXPRESSION; TWIST1;
D O I
10.1371/journal.pone.0157137
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Endothelium-dependent angiogenesis is thought to be a crucial step in cancer progression. We previously reported that metastasis-associated in colon cancer-1 (MACC1) contributed to the vasculogenic mimicry in gastric cancer (GC), but it remains unknown whether MACC1 promotes endothelium-dependent angiogenesis of GC and whether TWIST1 is involved in this process. In the present study, we detected MACC1 expression and microvessel density (MVD) by immunohistochemistry in 159 patients with stage I-III GC, and investigated the role of TWIST1 and vascular endothelial growth factor A (VEGF-A) in MACC1-induced endothelium-dependent angiogenesis using nude mice with GC xenografts, and human umbilical vein endothelial cells (HUVECs) that were co-cultured with conditioned media from overexpression and interference MACC1 GC cells. We found that MACC1 expression was positively correlated with an increased MVD and tumor recurrence in GC patients. In GC xenograft models, MACC1 elevated MVD and upregulated the expression of VEGF-A as well as accelerated tumor growth. In addition, MACC1 obviously increased the expression of TWIST1 and induced tube-like formation of HUVECs, whereas attenuation of TWIST1 suppressed the protein expression of VEGF-A and repealed the effect of MACC1 on tube formation. Our findings shed light on the function of MACC1 in endothelium-dependent angiogenesis of GC and suggest potential prognostic and therapeutic value.
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页数:17
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