Wang Lin, Zhou Rui, Zhao Yang, Dong Shaoting, Zhang Jingwen, Luo Yuhao, Huang Na, Shi Min, Bin Jianping, Liao Yulin, Liao Wangjun
Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
PLoS One. 2016 Jun 9;11(6):e0157137. doi: 10.1371/journal.pone.0157137. eCollection 2016.
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induced tube-like formation of HUVECs, whereas attenuation of TWIST1 suppressed the protein expression of VEGF-A and repealed the effect of MACC1 on tube formation.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.
内皮细胞依赖性血管生成被认为是癌症进展中的关键步骤。我们之前报道过,结肠癌转移相关蛋白1(MACC1)促成了胃癌(GC)中的血管生成拟态,但MACC1是否促进GC的内皮细胞依赖性血管生成以及TWIST1是否参与此过程仍不清楚。在本研究中,我们通过免疫组织化学检测了159例I-III期GC患者的MACC1表达和微血管密度(MVD),并使用GC异种移植裸鼠以及与过表达和干扰MACC1的GC细胞的条件培养基共培养的人脐静脉内皮细胞(HUVEC),研究了TWIST1和血管内皮生长因子A(VEGF-A)在MACC1诱导的内皮细胞依赖性血管生成中的作用。我们发现MACC1表达与GC患者MVD增加和肿瘤复发呈正相关。在GC异种移植模型中,MACC1提高了MVD,上调了VEGF-A的表达,并加速了肿瘤生长。此外,MACC1明显增加了TWIST1的表达并诱导了HUVEC的管状形成,而TWIST1的减弱则抑制了VEGF-A的蛋白表达并消除了MACC1对管状形成的影响。我们的研究结果揭示了MACC1在GC内皮细胞依赖性血管生成中的功能,并提示了潜在的预后和治疗价值。