New targets for pyrimidine antimetabolites for the treatment of solid tumours. 2: Deoxycytidine kinase
- PMID: 7980770
- DOI: 10.1007/BF01880661
New targets for pyrimidine antimetabolites for the treatment of solid tumours. 2: Deoxycytidine kinase
Erratum in
- Pharm World Sci 1994 Jun 10;16(3):168
Abstract
Deoxycytidine kinase is an enzyme required for the activation of, for example, cytarabine, the most widely used agent for the chemotherapy of haematological malignancies. However, deoxycytidine kinase also plays an important role in the activation of several new agents used in the treatment of leukaemia, such as cladribine. Recently, a new cytidine analogue, gemcitabine, has shown impressive activity as a single agent against several solid malignancies (ovarian cancer, non-small cell lung cancer), demonstrating that in solid tumours deoxycytidine kinase can be an important target for the activation of antimetabolites. Studies on the regulation of deoxycytidine kinase have shown that the enzyme has a complicated regulation (feedback inhibition by the product and regulation by ribonucleotides). Modulation of deoxycytidine kinase activity has already been shown to be an effective way to improve the effect of cytarabine and will probably be a target for new therapies.
Similar articles
-
[Metabolism, mechanism of action and resistance to cytotoxic nucleoside analogues].Bull Cancer. 2005 Mar;92(3):239-48. Bull Cancer. 2005. PMID: 15820918 Review. French.
-
Deoxycytidine kinase is downregulated under hypoxic conditions and confers resistance against cytarabine in acute myeloid leukaemia.Eur J Haematol. 2016 Sep;97(3):239-44. doi: 10.1111/ejh.12711. Epub 2015 Dec 28. Eur J Haematol. 2016. PMID: 26613208
-
Retroviral transfer of deoxycytidine kinase into tumor cell lines enhances nucleoside toxicity.Cancer Res. 1996 May 15;56(10):2343-7. Cancer Res. 1996. PMID: 8625309
-
Nucleoside analogues in the treatment of haematological malignancies.Expert Opin Pharmacother. 2001 Jun;2(6):929-43. doi: 10.1517/14656566.2.6.929. Expert Opin Pharmacother. 2001. PMID: 11585009 Review.
-
Impact of cytidine deaminase activity on intrinsic resistance to cytarabine in carcinoma cells.Oncol Rep. 2004 Nov;12(5):1115-20. Oncol Rep. 2004. PMID: 15492802
Cited by
-
In vivo toxicity study of N-1-sulfonylcytosine derivatives and their mechanisms of action in cervical carcinoma cell line.Invest New Drugs. 2012 Jun;30(3):981-90. doi: 10.1007/s10637-011-9657-x. Epub 2011 Mar 22. Invest New Drugs. 2012. PMID: 21424699
-
Structural and kinetic characterization of human deoxycytidine kinase variants able to phosphorylate 5-substituted deoxycytidine and thymidine analogues.Biochemistry. 2010 Aug 10;49(31):6784-90. doi: 10.1021/bi100839e. Biochemistry. 2010. PMID: 20614893 Free PMC article.
-
Molecular basis of 2',3'-dideoxycytidine-induced drug resistance in human cells.Mol Cell Biochem. 2002 Feb;231(1-2):173-7. doi: 10.1023/a:1014441209108. Mol Cell Biochem. 2002. PMID: 11952160
-
Drug resistance against gemcitabine and topotecan mediated by constitutive hsp70 overexpression in vitro: implication of quercetin as sensitiser in chemotherapy.Br J Cancer. 1996 Jul;74(2):172-7. doi: 10.1038/bjc.1996.334. Br J Cancer. 1996. PMID: 8688318 Free PMC article.
-
Increased sensitivity to gemcitabine of P-glycoprotein and multidrug resistance-associated protein-overexpressing human cancer cell lines.Br J Cancer. 2003 Jun 16;88(12):1963-70. doi: 10.1038/sj.bjc.6601011. Br J Cancer. 2003. PMID: 12799644 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources