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The Role of Membrane Transporters in Cellular Resistance to Anticancer Nucleoside Drugs

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Part of the book series: Cancer Treatment and Research ((CTAR,volume 112))

Abstract

Physiologic nucleosides and most therapeutic nucleoside analogs do not readily cross plasma membranes by passive diffusion due to their low solubility in lipid bilayers, and their cellular uptake is mediated by integral membrane proteins. Nucleoside transporters serve as the cellular entry point for nucleoside salvage pathways. Some cell types use these pathways exclusively because they lack the ability to synthesize purine and pyrimidine nucleotides. Other cell types use salvage pathways in addition to their de novo synthesis pathways. Nucleotides are key activated intermediates for many essential cellular biosynthetic pathways, including the synthesis of DNA and RNA

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Clarke, M.L., Mackey, J.R., Baldwin, S.A., Young, J.D., Cass, C.E. (2002). The Role of Membrane Transporters in Cellular Resistance to Anticancer Nucleoside Drugs. In: Andersson, B., Murray, D. (eds) Clinically Relevant Resistance in Cancer Chemotherapy. Cancer Treatment and Research, vol 112. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1173-1_2

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