Genetic markers inCYP2C19andCYP2B6for prediction of cyclophosphamide's 4-hydroxylation, efficacy and side effects in Chinese patients with systemic lupus erythematosus

Author:

Shu Wenying12,Guan Su3,Yang Xiuyan4,Liang Liuqin4,Li Jiali1,Chen Zhuojia1,Zhang Yu1,Chen Lingyan1,Wang Xueding1,Huang Min1

Affiliation:

1. Institute of Clinical Pharmacology, School of Pharmaceutical Sciences; Sun Yat-sen University; Guangzhou 510006

2. Department of Pharmacy; Cancer Center of Guangzhou Medical University; Guangzhou 510182

3. School of Bioscience and Biotechnology; South China University of Technology; Guangzhou 510006

4. Department of Rheumatology and Clinical Immunology; The First Affiliated Hospital of Sun Yat-sen University; Guangzhou 510080 China

Funder

National Natural Science Foundation of China

National Major Scientific and Technological Special Project

Fundamental Research Funds for the Central Universities

Guangzhou Medical University Scientific Research Program for Young Scientists

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference47 articles.

1. Cyclophosphamide: new approaches for systemic lupus erythematosus;Petri;Lupus,2004

2. Strategies for preservation of ovarian and testicular function after immunosuppression;Pendse;Am J Kidney Dis,2004

3. Relationship of glutathione S-transferase genotypes with side-effects of pulsed cyclophosphamide therapy in patients with systemic lupus erythematosus;Zhong;Br J Clin Pharmacol,2006

4. Role of polymorphic human CYP2B6 in cyclophosphamide bioactivation;Xie;Pharmacogenomics J,2003

5. Development of a substrate-activity based approach to identify the major human liver P-450 catalysts of cyclophosphamide and ifosfamide activation based on cDNA-expressed activities and liver microsomal P-450 profiles;Roy;Drug Metab Dispos,1999

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