Wang Xian, Zhang Tiran, Yu Rong
Image Center, Mudanjiang Cancer Hospital, Heilongjiang, PR China.
Department of Thyroid and Breast Surgery, Xinghua People's Hospital, Taizhou, Jiangsu, PR China.
Histol Histopathol. 2025 Mar;40(3):343-356. doi: 10.14670/HH-18-779. Epub 2024 Jun 12.
Gastric cancer represents an aggressive malignancy and a leading contributor to cancer death. Ephrin-A4 (EFNA4) has been proposed to be related to the immune microenvironment and prognosis of gastric cancer. This study was undertaken to discuss the participation and mechanism of EFNA4 in the development of gastric cancer. RT-qPCR and western blot examined EFNA4 and Pygopus2 (Pygo2) expression in gastric cancer cells. After transfection of EFNA4 interference plasmids or co-transfection of EFNA4 interference plasmids and Pygo2 overexpression plasmids, cell proliferation was detected by the CCK-8 method and EDU staining. Wound healing, Transwell, TUNEL, and endothelial cell tube formation assays detected cell migration, invasion, apoptosis, and angiogenesis, respectively. Western blot examined the expression of metastasis-, apoptosis-, angiogenesis-, and Wnt signaling-associated proteins. Cell stemness was estimated by the sphere formation assay, RT-qPCR, and western blot. Through the experimental data, it was noticed that EFNA4 expression was increased in gastric cancer cells. Knockdown of EFNA4 suppressed the proliferation, migration, invasion, angiogenesis as well as stemness while aggravating the apoptosis of gastric cancer cells. Also, EFNA4 depletion reduced Pygo2 protein expression and then inactivated Wnt/β-catenin signaling. Further elevation of Pygo2 reversed the impacts of EFNA4 silencing on Wnt/β-catenin signaling, cell proliferation, apoptosis, migration, invasion, angiogenesis as well as stemness in gastric cancer. Accordingly, the knockdown of EFNA4 might downregulate Pygo2 and inactivate Wnt/β-catenin signaling to exert protective effects against gastric cancer.
胃癌是一种侵袭性恶性肿瘤,也是导致癌症死亡的主要原因。有人提出, Ephrin-A4(EFNA4)与胃癌的免疫微环境和预后有关。本研究旨在探讨EFNA4在胃癌发生发展中的作用及机制。采用RT-qPCR和蛋白质免疫印迹法检测胃癌细胞中EFNA4和Pygopus2(Pygo2)的表达。转染EFNA4干扰质粒或共转染EFNA4干扰质粒与Pygo2过表达质粒后,采用CCK-8法和EDU染色检测细胞增殖情况。划痕实验、Transwell实验、TUNEL实验和内皮细胞成管实验分别检测细胞迁移、侵袭、凋亡和血管生成情况。蛋白质免疫印迹法检测与转移、凋亡、血管生成和Wnt信号相关蛋白的表达。通过成球实验、RT-qPCR和蛋白质免疫印迹法评估细胞干性。通过实验数据发现,胃癌细胞中EFNA4表达增加。敲低EFNA4可抑制胃癌细胞的增殖、迁移、侵袭、血管生成以及干性,同时加重细胞凋亡。此外,EFNA4缺失降低了Pygo2蛋白表达,进而使Wnt/β-连环蛋白信号失活。Pygo2的进一步上调逆转了EFNA4沉默对胃癌细胞中Wnt/β-连环蛋白信号通路、细胞增殖、凋亡、迁移、侵袭、血管生成以及干性的影响。因此,敲低EFNA4可能下调Pygo2并使Wnt/β-连环蛋白信号失活,从而对胃癌发挥保护作用。