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Study of intracellular anabolism of 5-fluorouracil and incorporation in nucleic acids based on an LC-HRMS method

摘要5-Fluorouracil(5-FU)is an anticancer drug extensively used for different cancers.Intracellular metabolic activation leads to several nucleoside and nucleotide metabolites essential to exert its cytotoxic activity on multiple cellular targets such as enzymes,DNA and RNA.In this paper,we describe the development of a method based on liquid chromatography coupled with high resolution mass spectrometry suitable for the simultaneous determination of the ten anabolic metabolites(nucleoside,nucleotide and sugar nucleotide)of 5-FU.The chromatographic separation was optimized on a porous graphitic carbon column allowing the analysis of the metabolites of 5-FU as well as endogenous nucleotides.The detection was performed on an Orbitrap? tandem mass spectrometer.Linearity of the method was verified in intra-cellular content and in RNA extracts.The limit of detection was equal to 12 pg injected on column for nucleoside metabolites of 5-FU and 150 pg injected on column for mono-and tri-phosphate nucleotide metabolites.Matrix effect was evaluated in cellular contents,DNA and RNA extracts for nucleoside and nucleotides metabolites.The method was successfully applied to i)measure the proportion of each anabolic metabolite of 5-FU in cellular contents,ii)follow the consequence of inhibition of enzymes on the endogenous nucleotide pools,iii)study the incorporation of metabolites of 5-FU into RNA and DNA,and iv)to determine the incorporation rate of 5-FUrd into 18 S and 28 S sub-units of rRNA.

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作者 Christelle Machon [1] Frédéric Catez [2] Nicole Dalla Venezia [2] Floriane Vanhalle [3] Laetitia Guyot [3] Anne Vincent [2] Maxime Garcia [2] Béatrice Roy [4] Jean-Jacques Diaz [2] Jér?me Guitton [5] 学术成果认领
作者单位 Laboratoire de Chimie Analytique, Faculté de Pharmacie de Lyon, Université Lyon 1, 8 Avenue Rockefeller, Lyon, 69373, France;Laboratoire de Biochimie et de Pharmaco-toxicologie, Centre Hospitalier Lyon -Sud-HCL, Pierre Benite, 69495, France;Inserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France. Centre Léon Bérard, F-69008 Lyon, France, Universitéde Lyon 1, F-69000 Lyon, France [1] Inserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France. Centre Léon Bérard, F-69008 Lyon, France, Universitéde Lyon 1, F-69000 Lyon, France [2] Laboratoire de Biochimie et de Pharmaco-toxicologie, Centre Hospitalier Lyon -Sud-HCL, Pierre Benite, 69495, France [3] Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS, Université de Montpellier, ENSCM, Campus Triolet, Montpellier, France [4] Laboratoire de Biochimie et de Pharmaco-toxicologie, Centre Hospitalier Lyon -Sud-HCL, Pierre Benite, 69495, France;Inserm U1052, CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France. Centre Léon Bérard, F-69008 Lyon, France, Universitéde Lyon 1, F-69000 Lyon, France;Laboratoire de toxicologie, Faculté de pharmacie de Lyon, 8 avenue Rockefeller, F-69373 Lyon, France [5]
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发布时间 2021-03-30(万方平台首次上网日期,不代表论文的发表时间)
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药物分析学报(英文)

药物分析学报(英文)

2021年11卷1期

77-87页

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