CYP17A1型
CYP3A4型
前列腺癌
醋酸阿比特龙酯
单核苷酸多态性
生物
癌症研究
SNP公司
基因
内科学
细胞色素P450
雄激素剥夺疗法
药理学
基因型
内分泌学
肿瘤科
癌症
医学
遗传学
新陈代谢
作者
Sisi Qin,Duan Liu,Manish Kohli,Liguo Wang,Peter T. Vedell,David W. Hillman,Nifang Niu,Jia Yu,Richard M. Weinshilboum,Liewei Wang,Liewei Wang,Liewei Wang
摘要
The testis‐specific Y‐encoded‐like protein ( TSPYL ) gene family includes TSPYL1 to TSPYL6 . We previously reported that TSPYL5 regulates cytochrome P450 (CYP) 19A1 expression. Here we show that TSPYLs, especially TSPYL 1, 2, and 4, can regulate the expression of many CYP genes, including CYP17A1, a key enzyme in androgen biosynthesis, and CYP3A4, an enzyme that catalyzes the metabolism of abiraterone, a CYP17 inhibitor. Furthermore, a common TSPYL1 single nucleotide polymorphism (SNP), rs3828743 (G/A) (Pro62Ser), abolishes TSPYL1's ability to suppress CYP3A4 expression, resulting in reduced abiraterone concentrations and increased cell proliferation. Data from a prospective clinical trial of 87 metastatic castration‐resistant prostate cancer patients treated with abiraterone acetate/prednisone showed that the variant SNP genotype (A) was significantly associated with worse response and progression‐free survival. In summary, TSPYL genes are novel CYP gene transcription regulators, and genetic alteration within these genes significantly influences response to drug therapy through transcriptional regulation of CYP450 genes.
科研通智能强力驱动
Strongly Powered by AbleSci AI