Department of Stomatology, Tianjin Third Central Hospital, Hedong District, Tianjin, PR China.
Histol Histopathol. 2024 Apr;39(4):463-470. doi: 10.14670/HH-18-637. Epub 2023 Jun 6.
Eukaryotic translation initiation factor 5A2 (EIF5A2) has been reported to be involved in metastasis and chemotherapy resistance in many human cancers. However, the effect and mechanism of EIF5A2 in oral cancer cells are unknown. Here, we investigated the effects of targeting EIF5A2 on chemotherapy resistance in oral cancer cells .
By using a lentiviral system, we investigated the effects of targeting EIF5A2 on the invasion, migration, growth, and chemosensitivity of SCC-9 cells to CDDP . Through the method of gene intervention, we explore the role of pro-apoptotic Bim and epithelial and mesenchymal marker E-cadherin protein in this process and the regulation of EIF5A2 on Bim and E-cadherin.
Targeting EIF5A2 reduces invasion and migration in SCC-9 cells partly through upregulation of E-cadherin expression; Targeting EIF5A2 promotes cell apoptosis and inhibits cell survival as well as increasing chemosensitivity in SCC-9 cells through upregulation of Bim expression.
EIF5A2 may be a novel potential therapeutic target for oral cancer by upregulation of Bim and E-cadherin.
真核翻译起始因子 5A2(EIF5A2)已被报道参与多种人类癌症的转移和化疗耐药。然而,EIF5A2 在口腔癌细胞中的作用和机制尚不清楚。在这里,我们研究了靶向 EIF5A2 对口腔癌细胞化疗耐药性的影响。
我们通过慢病毒系统研究了靶向 EIF5A2 对 SCC-9 细胞对 CDDP 的侵袭、迁移、生长和化疗敏感性的影响。通过基因干预的方法,我们探讨了促凋亡蛋白 Bim 和上皮-间充质标志物 E-钙黏蛋白在这一过程中的作用,以及 EIF5A2 对 Bim 和 E-钙黏蛋白的调节作用。
靶向 EIF5A2 可部分通过上调 E-钙黏蛋白表达降低 SCC-9 细胞的侵袭和迁移;靶向 EIF5A2 通过上调 Bim 表达促进细胞凋亡、抑制细胞存活并增加 SCC-9 细胞的化疗敏感性。
通过上调 Bim 和 E-钙黏蛋白,EIF5A2 可能成为口腔癌的一种新的潜在治疗靶点。