Juknevičienė Milda, Balnytė Ingrida, Valančiūtė Angelija, Alonso Marta Marija, Preikšaitis Aidanas, Sužiedėlis Kęstutis, Stakišaitis Donatas
Department of Histology and Embryology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.
Department of Pediatrics, Clínica Universidad de Navarra, University of Navarra, 31008 Pamplona, Spain.
Biomedicines. 2024 Jun 25;12(7):1416. doi: 10.3390/biomedicines12071416.
Valproic acid (VPA) has anticancer, anti-inflammatory, and epigenetic effects. The study aimed to determine the expression of carcinogenesis-related , , , and in adult glioblastoma U87 MG and T98G cells and the effects of 0.5 mM, 0.75 mM, and 1.5 mM doses of VPA. RNA gene expression was determined by RT-PCR. was used as a control. U87 and T98G control cells do not express or was expressed in U87 control but not in T98G control cells. The expression in the U87 control was significantly lower than in the T98G control. T98G control cells showed significantly higher expression than U87 control cells. VPA treatment did not affect expression in U87 cells, whereas treatment dose-dependently increased expression in T98G cells. Treatment with 1.5 mM VPA induced expression in U87 cells, while treatment of T98G cells with VPA did not affect expression. Treatment of U87 cells with VPA significantly increased expression. VPA increases expression depending on the VPA dose. expression was significantly increased only in the U87 1.5 mM VPA group. Tested VPA doses significantly increased expression in T98G cells. When approaching treatment tactics, assessing the cell's sensitivity to the agent is essential.
丙戊酸(VPA)具有抗癌、抗炎和表观遗传作用。该研究旨在确定成人间变性星形细胞瘤U87 MG和T98G细胞中与致癌作用相关的[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]和[此处原文缺失具体基因名称]的表达情况,以及0.5 mM、0.75 mM和1.5 mM剂量的VPA的作用。通过逆转录聚合酶链反应(RT-PCR)测定RNA基因表达。[此处原文缺失用作对照的具体内容]用作对照。U87和T98G对照细胞不表达[此处原文缺失具体基因名称],[此处原文缺失具体基因名称]在U87对照细胞中表达,但在T98G对照细胞中不表达。U87对照细胞中的[此处原文缺失具体基因名称]表达明显低于T98G对照细胞。T98G对照细胞显示出比U87对照细胞明显更高的[此处原文缺失具体基因名称]表达。VPA处理不影响U87细胞中的[此处原文缺失具体基因名称]表达,而处理在T98G细胞中剂量依赖性地增加[此处原文缺失具体基因名称]表达。用1.5 mM VPA处理诱导U87细胞中的[此处原文缺失具体基因名称]表达,而用VPA处理T98G细胞不影响[此处原文缺失具体基因名称]表达。用VPA处理U87细胞显著增加[此处原文缺失具体基因名称]表达。VPA根据VPA剂量增加[此处原文缺失具体基因名称]表达。仅在U87 1.5 mM VPA组中[此处原文缺失具体基因名称]表达显著增加。测试的VPA剂量显著增加T98G细胞中的[此处原文缺失具体基因名称]表达。在制定治疗策略时,评估细胞对药物的敏感性至关重要。