Mao Xiang, Wang Jun, Luo Fen
Department of General Surgery, Huashan Hospital, Shanghai, 200040, China.
Department of General Surgery, Huashan Hospital, No. 12, Middle Urumqi Road, Shanghai, 200040, China.
Open Life Sci. 2023 Aug 10;18(1):20220476. doi: 10.1515/biol-2022-0476. eCollection 2023.
This study aimed to investigate whether α-fetoprotein (AFP) could affect the malignant behavior of AFP-producing gastric cancer (AFP-GC) and to explore the relationship between AFP and mesenchymal-epithelial transition factor (c-Met) in AFP-GC. In this study, 23 patients with AFP-GC (AFP[+]) and 18 patients with common gastric cancer (AFP[-]) were evaluated for the c-Met expression using immunohistochemical analysis. The AFP-GC cell line, GCIY, was used. The AFP endoribonuclease-prepared small interfering RNA (siRNA) and eukaryotic AFP overexpression vector were used to increase/knockdown the expression of AFP. Afterward, the c-Met expression was evaluated by polymerase chain reaction and western blot. The proliferation, migration, and invasion of GCIY cells were estimated before and after the AFP overexpression/knockdown. The c-Met expression in both groups was the same ( > 0.05), and AFP[+] group had a higher positive incidence of the c-Met expression than the AFP[-] group ( < 0.01). Furthermore, the c-Met expression frequency was decreased by AFP knockdown and increased by AFP overexpression ( < 0.01). The cell counting kit-8 cell proliferation assay, cell invasion, and migration assays confirmed that the AFP could affect the malignant biological behavior of AFP-GC. These findings suggest that AFP contributes to the malignant biological properties of AFP-GC and the high expression of c-Met in AFP-GC.
本研究旨在探讨甲胎蛋白(AFP)是否会影响产AFP胃癌(AFP-GC)的恶性行为,并探究AFP与AFP-GC中间质上皮转化因子(c-Met)之间的关系。本研究采用免疫组化分析评估了23例AFP-GC患者(AFP[+])和18例普通胃癌患者(AFP[-])的c-Met表达情况。使用了AFP-GC细胞系GCIY。利用AFP核糖核酸酶制备的小干扰RNA(siRNA)和真核AFP过表达载体来增加/敲低AFP的表达。随后,通过聚合酶链反应和蛋白质免疫印迹法评估c-Met的表达。在AFP过表达/敲低前后评估GCIY细胞的增殖、迁移和侵袭能力。两组的c-Met表达情况相同(>0.05),但AFP[+]组c-Met表达的阳性发生率高于AFP[-]组(<0.01)。此外,AFP敲低可降低c-Met表达频率,AFP过表达则使其增加(<0.01)。细胞计数试剂盒-8细胞增殖试验、细胞侵袭和迁移试验证实,AFP可影响AFP-GC的恶性生物学行为。这些研究结果表明,AFP促成了AFP-GC的恶性生物学特性以及AFP-GC中c-Met的高表达。