Intracellular pharmacokinetics of gemcitabine, its deaminated metabolite 2′,2′-difluorodeoxyuridine and their nucleotides

Author:

Derissen Ellen J. B.12ORCID,Huitema Alwin D. R.13,Rosing Hilde1,Schellens Jan H. M.45,Beijnen Jos H.15

Affiliation:

1. Department of Pharmacy & Pharmacology; Antoni van Leeuwenhoek Hospital - The Netherlands Cancer Institute and MC Slotervaart; Louwesweg 6, 1066 EC Amsterdam The Netherlands

2. Department of Clinical Pharmacology and Pharmacy; VU University Medical Center; De Boelelaan 1117 1081 HV Amsterdam The Netherlands

3. Department of Clinical Pharmacy; University Medical Center Utrecht; Heidelberglaan 100 3584 CX Utrecht The Netherlands

4. Department of Clinical Pharmacology; The Netherlands Cancer Institute; Plesmanlaan 121 1066 CX Amsterdam The Netherlands

5. Science Faculty, Utrecht Institute for Pharmaceutical Sciences (UIPS), Division of Pharmaco-epidemiology & Clinical Pharmacology; Utrecht University; P.O. Box 80082 3508 TB Utrecht The Netherlands

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference47 articles.

1. Functional nucleoside transporters are required for gemcitabine influx and manifestation of toxicity in cancer cell lines;Mackey;Cancer Res,1998

2. Recent molecular advances in studies of the concentrative Na+-dependent nucleoside transporter (CNT) family: identification and characterization of novel human and mouse proteins (hCNT3 and mCNT3) broadly selective for purine and pyrimidine nucleosides;Ritzel;Mol Membr Biol,2001

3. Clinical pharmacology and pharmacogenetics of gemcitabine;Wong;Drug Metab Rev,2009

4. Excision of 2′,2′-difluorodeoxycytidine (gemcitabine) monophosphate residues from DNA;Gandhi;Cancer Res,1996

5. Action of 2′,2′-difluorodeoxycytidine on DNA synthesis;Huang;Cancer Res,1991

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