Yin Jie, Cui Yuxin, Li Liting, Ji Jiafu, Jiang Wen G
Cardiff China Medical Research Collaborative, Cardiff University School of Medicine, Cardiff, U.K.
Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing, P.R. China.
Anticancer Res. 2017 Aug;37(8):4489-4497. doi: 10.21873/anticanres.11845.
Increased expression of erythropoietin-producing human hepatoma (EPHB4) leads to enhanced cell migration, growth and adhesion in tumor cells. However, little is known regarding the effects of EPHB4 in gastric cancer. The present study aimed to examine the clinical relevance of EPHB4 and its association with the prognosis of gastric cancer.
EPHB4 transcript expression in 324 gastric cancer samples with paired adjacent normal gastric tissues was determined using quantitative polymerase chain reaction and the results were statistically analyzed against patient clinicopathological data. AGS and HGC27 cell lines were transfected with EPHB4 siRNA and the effects examined by functional analysis.
EPHB4 mRNA levels in gastric cancer tissues were significantly elevated when compared to non-cancerous tissues (p=0.0110). Tissue samples from male patients exhibited lower expression than those from female patients (p=0.0110). Non-cardiac gastric tumors (fundus, corpus and pylorus) expressed a higher number of EPHB4 transcripts in comparison to cardiac gastric tumors (p<0.001). Increased expression of EPHB4 was significantly associated with poorer overall (p=0.0051) and progression-free (p=0.0262) survival. EPHB4 knockdown appeared to reduce post-wound migration of AGS cells (p=0.0057) and increase migration of HGC27 cells (p=0.0337). EPHB4 knockdown significantly increased adhesive ability in HGC27 (p<0.0001).
The expression of EPHB4 was increased in gastric cancer and increased EPHB4 expression was correlated with poor survival. Knockdown of EPHB4 promoted adhesion and exerted diverse effects on migration of gastric cancer cells. Further investigations may highlight its predictive and therapeutic potential in gastric cancer.
促红细胞生成素产生性人肝癌(EPHB4)表达增加会导致肿瘤细胞的迁移、生长和黏附增强。然而,关于EPHB4在胃癌中的作用知之甚少。本研究旨在探讨EPHB4的临床相关性及其与胃癌预后的关系。
采用定量聚合酶链反应测定324例胃癌样本及其配对的相邻正常胃组织中EPHB4转录本的表达,并针对患者的临床病理数据进行统计学分析。用EPHB4小干扰RNA转染AGS和HGC27细胞系,并通过功能分析检测其效果。
与非癌组织相比,胃癌组织中EPHB4 mRNA水平显著升高(p = 0.0110)。男性患者的组织样本表达低于女性患者(p = 0.0110)。与贲门部胃癌相比,非贲门部胃癌(胃底、胃体和幽门)表达的EPHB4转录本数量更多(p < 0.001)。EPHB4表达增加与较差的总生存期(p = 0.0051)和无进展生存期(p = 0.0262)显著相关。敲低EPHB似乎会减少AGS细胞的创伤后迁移(p = 0.0057),并增加HGC27细胞的迁移(p = 0.0337)。敲低EPHB4显著增加了HGC27细胞的黏附能力(p < 0.0001)。
EPHB4在胃癌中表达增加,且EPHB4表达增加与不良预后相关。敲低EPHB4可促进黏附,并对胃癌细胞的迁移产生不同影响。进一步的研究可能会突出其在胃癌中的预测和治疗潜力。