Literature DB >> 28318037

Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency.

Carlos Lopez-Gomez1, Rebecca J Levy1, Maria J Sanchez-Quintero1, Martí Juanola-Falgarona1, Emanuele Barca1,2, Beatriz Garcia-Diaz1,3, Saba Tadesse1, Caterina Garone1,4, Michio Hirano1.   

Abstract

OBJECTIVE: Thymidine kinase 2 (TK2), a critical enzyme in the mitochondrial pyrimidine salvage pathway, is essential for mitochondrial DNA (mtDNA) maintenance. Mutations in the nuclear gene, TK2, cause TK2 deficiency, which manifests predominantly in children as myopathy with mtDNA depletion. Molecular bypass therapy with the TK2 products, deoxycytidine monophosphate (dCMP) and deoxythymidine monophosphate (dTMP), prolongs the life span of Tk2-deficient (Tk2-/- ) mice by 2- to 3-fold. Because we observed rapid catabolism of the deoxynucleoside monophosphates to deoxythymidine (dT) and deoxycytidine (dC), we hypothesized that: (1) deoxynucleosides might be the major active agents and (2) inhibition of deoxycytidine deamination might enhance dTMP+dCMP therapy.
METHODS: To test these hypotheses, we assessed two therapies in Tk2-/- mice: (1) dT+dC and (2) coadministration of the deaminase inhibitor, tetrahydrouridine (THU), with dTMP+dCMP.
RESULTS: We observed that dC+dT delayed disease onset, prolonged life span of Tk2-deficient mice and restored mtDNA copy number as well as respiratory chain enzyme activities and levels. In contrast, dCMP+dTMP+THU therapy decreased life span of Tk2-/- animals compared to dCMP+dTMP.
INTERPRETATION: Our studies demonstrate that deoxynucleoside substrate enhancement is a novel therapy, which may ameliorate TK2 deficiency in patients. Ann Neurol 2017;81:641-652.
© 2017 American Neurological Association.

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Year:  2017        PMID: 28318037      PMCID: PMC5926768          DOI: 10.1002/ana.24922

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  25 in total

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3.  Heart mitochondrial TTP synthesis and the compartmentalization of TMP.

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4.  Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation.

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Review 5.  Defects in mitochondrial DNA replication and human disease.

Authors:  William C Copeland
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Review 6.  Thymidine kinase 2 enzyme kinetics elucidate the mechanism of thymidine-induced mitochondrial DNA depletion.

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8.  Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient mice.

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9.  Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency.

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10.  Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.

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Journal:  Neurology       Date:  2002-10-22       Impact factor: 9.910

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10.  Synergistic Deoxynucleoside and Gene Therapies for Thymidine Kinase 2 Deficiency.

Authors:  Carlos Lopez-Gomez; Maria J Sanchez-Quintero; Eung Jeon Lee; Giulio Kleiner; Saba Tadesse; Jun Xie; Hasan Orhan Akman; Guangping Gao; Michio Hirano
Journal:  Ann Neurol       Date:  2021-08-13       Impact factor: 11.274

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