细胞色素P450
CYP3A4型
肝细胞癌
CYP1A2
P-糖蛋白
基因表达
运输机
药物代谢
ATP结合盒运输机
生物
药理学
CYP2E1
Abcg2型
癌症研究
信使核糖核酸
基因
多重耐药
分子生物学
抗药性
药品
内分泌学
新陈代谢
遗传学
作者
Katsuhito Nagai,Shuhei Fukuno,Takeshi Miura,Eri Yasuda-Imanishi,Hiroki Konishi
出处
期刊:Drug research
[Georg Thieme Verlag KG]
日期:2023-08-17
卷期号:73 (08): 473-475
摘要
Bardoxolone methyl (BX) is expected to be an innovate therapeutic agent for chronic kidney disease (CKD). The aim of the present study was to examine whether the expression of subtypes of cytochrome P450 (CYP) and ABC transporters was altered in human hepatocellular carcinoma HepG2 cells by exposure to BX. The expression of mRNAs for CYP1A2, CYP2E1, P-glycoprotein, multidrug resistance-associated protein 1-3, and breast cancer resistance protein was significantly increased by exposure of HepG2 cells to BX, while the expression of CYP3A4 mRNA was significantly decreased under the same conditions. BX had no significant effect on the expression of mRNAs for CYP2C9 and CYP2C19 in HepG2 cells. In conclusion, this study demonstrated that the gene expression of several CYPs and ABC transporters in HepG2 cells was altered when exposed to BX, suggesting the need to pay careful attention to drug-drug interactions in patients receiving BX for CKD treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI