羧酸酯酶1和2基因多态性在药物代谢中的研究进展

被引:7
作者
刘帅兵 [1 ,2 ]
缪丽燕 [1 ,2 ]
机构
[1] 苏州大学附属第一医院临床药理研究室
[2] 苏州大学药学院
关键词
羧酸酯酶1; 羧酸酯酶2; 药物代谢; 单核苷酸多态性;
D O I
10.19577/j.cnki.issn10074406.2015.03.017
中图分类号
R96 [药理学];
学科分类号
100706 [药理学];
摘要
人类羧酸酯酶属于α/β水解酶家族,负责许多内源性和外源性化合物的水解,广泛位于药物代谢的主要组织,例如肝脏和小肠等。人羧酸酯酶主要有羧酸酯酶1(CES1)和2(CES2)。单核苷酸多态性(SNPs)对药物代谢酶的表达和(或)活性有重要的影响,这可能解释部分药物反应的个体差异。本篇综述主要介绍了由CES1和CES2单核苷酸多态性导致的CES酶多态性。对于含有酯键的药物,一些有意义的SNP可能影响CES酶的功能从而影响其药动学,进而对其药理和毒理作用发挥重要影响。
引用
收藏
页码:206 / 210
页数:5
相关论文
共 18 条
[1]
羧酸酯酶基因1多态性鉴定及其与抗结核药物肝毒性相关性研究.[J].吴雪琼;朱冬林;张俊仙;钟逾;席云;安慧茹;梁艳;阳幼荣;.中华内科杂志.2012, 07
[2]
The effects of CES1A2 A(-816)C and CYP2C19 loss-of-function polymorphisms on clopidogrel response variability among Chinese patients with coronary heart disease [J].
Xie, Cheng ;
Ding, Xiaoliang ;
Gao, Jie ;
Wang, Haipeng ;
Hang, Yongfu ;
Zhang, Hua ;
Zhang, Jingjing ;
Jiang, Bin ;
Miao, Liyan .
PHARMACOGENETICS AND GENOMICS, 2014, 24 (04) :204-210
[3]
CES1A -816C as a Genetic Marker to Predict Greater Platelet Clopidogrel Response in Patients with Percutaneous Coronary Intervention [J].
Zou, Jian-Jun ;
Chen, Shao-Liang ;
Fan, Hong-Wei ;
Tan, Jie ;
He, Bang-Shun ;
Xie, Hong-Guang .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2014, 63 (02) :178-183
[4]
Genetic Determinants of Dabigatran Plasma Levels and Their Relation to Bleeding [J].
Pare, Guillaume ;
Eriksson, Niclas ;
Lehr, Thorsten ;
Connolly, Stuart ;
Eikelboom, John ;
Ezekowitz, Michael D. ;
Axelsson, Tomas ;
Haertter, Sebastian ;
Oldgren, Jonas ;
Reilly, Paul ;
Siegbahn, Agneta ;
Syvanen, Ann-Christine ;
Wadelius, Claes ;
Wadelius, Mia ;
Zimdahl-Gelling, Heike ;
Yusuf, Salim ;
Wallentin, Lars .
CIRCULATION, 2013, 127 (13) :1404-+
[5]
The functional G143E variant of carboxylesterase 1 is associated with increased clopidogrel active metabolite levels and greater clopidogrel response [J].
Lewis, Joshua P. ;
Horenstein, Richard B. ;
Ryan, Kathleen ;
O'Connell, Jeffrey R. ;
Gibson, Quince ;
Mitchell, Braxton D. ;
Tanner, Keith ;
Chai, Sumbul ;
Bliden, Kevin P. ;
Tantry, Udaya S. ;
Peer, Cody J. ;
Figg, William D. ;
Spencer, Shawn D. ;
Pacanowski, Michael A. ;
Gurbel, Paul A. ;
Shuldiner, Alan R. .
PHARMACOGENETICS AND GENOMICS, 2013, 23 (01) :1-8
[6]
Association of carboxylesterase 1A genotypes with irinotecan pharmacokinetics in Japanese cancer patients [J].
Sai, Kimie ;
Saito, Yoshiro ;
Tatewaki, Naoko ;
Hosokawa, Masakiyo ;
Kaniwa, Nahoko ;
Nishimaki-Mogami, Tomoko ;
Naito, Mikihiko ;
Sawada, Jun-ichi ;
Shirao, Kuniaki ;
Hamaguchi, Tetsuya ;
Yamamoto, Noboru ;
Kunitoh, Hideo ;
Tamura, Tomohide ;
Yamada, Yasuhide ;
Ohe, Yuichiro ;
Yoshida, Teruhiko ;
Minami, Hironobu ;
Ohtsu, Atsushi ;
Matsumura, Yasuhiro ;
Saijo, Nagahiro ;
Okuda, Haruhiro .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 70 (02) :222-233
[7]
Carboxylesterase 1 gene polymorphism and methylphenidate response in ADHD.[J].Zsofia Nemoda;Nora Angyal;Zsanett Tarnok;Julia Gadoros;Maria Sasvari-Szekely.Neuropharmacology.2009, 7
[8]
Influence of carboxylesterase 2 genetic polymorphisms on mycophenolic acid pharmacokinetics in Japanese renal transplant recipients [J].
Fujiyama, N. ;
Miura, M. ;
Satoh, S. ;
Inoue, K. ;
Kagaya, H. ;
Saito, M. ;
Habuchi, T. ;
Suzuki, T. .
XENOBIOTICA, 2009, 39 (05) :407-414
[9]
Structure and characterization of human carboxylesterase 1A1, 1A2, and 1A3 genes [J].
Fukami, Tatsuki ;
Nakajima, Miki ;
Maruichi, Taiga ;
Takahashi, Shiori ;
Takamiya, Masataka ;
Aoki, Yasuhiro ;
McLeod, Howard L. ;
Yokoi, Tsuyoshi .
PHARMACOGENETICS AND GENOMICS, 2008, 18 (10) :911-920
[10]
Role of carboxylesterase 1 and impact of natural genetic variants on the hydrolysis of trandolapril.[J].Hao-Jie Zhu;David I. Appel;Julie A. Johnson;Kenneth D. Chavin;John S. Markowitz.Biochemical Pharmacology.2008, 7