Department of Neurology, Xiangyang First People's Hospital of Hubei University, Xiangyang, Hubei, China.
Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820980104. doi: 10.1177/1533033820980104.
Our study was designed to investigate the role of B4GalT1 in glioblastoma, in vitro and in vivo, to detect whether B4GalT1 knockdown could regulate the development of glioblastoma, and further observe the relationship between B4GalT1 knockdown and the apoptosis and autophagy of glioblastoma. To begin, we looked at TCGA and GEPIA systems to predict the potential function of B4GalT1. Western blot and RT-PCR were used to analyze the expression, or mRNA level, of B4GalT1 at different tissue or cell lines. Next, the occurrence and development of glioblastoma, in vitro and in vivo, was observed by using B4GalT1 knocked down by lentivirus. Finally, the apoptosis and autophagy of glioblastoma was observed in vitro and in vivo. Results show that B4GalT1 was a highly variable gene, and GEPIA and TCGA systems show B4GalT1 expression in GBM tumor tissue was higher than in normal tissue. Pair-wise gene correlation analysis revealed a probable relationship between B4GalT1 and autophagy related proteins. The B4GalT1 expression and mRNA level were increased in tumor cells, or U87 cells. B4GalT1 knocked down by lentivirus could inhibit glioblastoma development, in vitro and in vivo, by reducing tumor weight and volume, increasing survival, and weakening tumor cells proliferation, migration, invasion. B4GalT1 knockdown could increase apoptosis and autophagy of glioblastoma in vitro and in vivo. Our study demonstrates that B4GalT1 may be able to regulate apoptosis and autophagy of glioblastoma. Bax, Bcl-2, cleaved caspase-3, Beclin-1, and LC3 s may be the downstream target factors of B4GalT1 in apoptosis and autophagy, which may provide a new strategy to reduce glioblastoma development by regulating apoptosis and autophagy.
我们的研究旨在探讨 B4GalT1 在胶质母细胞瘤中的作用,包括在体外和体内的作用,以检测 B4GalT1 敲低是否能调节胶质母细胞瘤的发展,并进一步观察 B4GalT1 敲低与胶质母细胞瘤凋亡和自噬的关系。首先,我们通过 TCGA 和 GEPIA 系统来预测 B4GalT1 的潜在功能。通过 Western blot 和 RT-PCR 分析不同组织或细胞系中 B4GalT1 的表达或 mRNA 水平。接下来,通过慢病毒敲低 B4GalT1 观察胶质母细胞瘤的发生和发展,包括在体外和体内。最后,观察胶质母细胞瘤在体外和体内的凋亡和自噬。结果表明,B4GalT1 是一个高度可变的基因,GEPIA 和 TCGA 系统显示 B4GalT1 在 GBM 肿瘤组织中的表达高于正常组织。基因相关性分析显示,B4GalT1 与自噬相关蛋白可能存在一定的关系。肿瘤细胞或 U87 细胞中 B4GalT1 的表达和 mRNA 水平均升高。慢病毒敲低 B4GalT1 可以通过减少肿瘤重量和体积、增加存活率、减弱肿瘤细胞增殖、迁移和侵袭,抑制体外和体内胶质母细胞瘤的发展。B4GalT1 敲低可以增加体外和体内胶质母细胞瘤的凋亡和自噬。我们的研究表明,B4GalT1 可能能够调节胶质母细胞瘤的凋亡和自噬。Bax、Bcl-2、cleaved caspase-3、Beclin-1 和 LC3s 可能是 B4GalT1 在凋亡和自噬中的下游靶标因子,这可能为通过调节凋亡和自噬来减少胶质母细胞瘤的发展提供新的策略。