The 5′-nucleotidases as regulators of nucleotide and drug metabolism

被引:225
作者
Hunsucker, SA
Mitchell, BS
Spychala, J
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Pharmacol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
关键词
nucleotidase; nucleoside metabolism; nucleoside analogues;
D O I
10.1016/j.pharmthera.2005.01.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 5'-nucleotidases are a family of enzymes that catalyze the dephosphorylation of nucleoside monophosphates and regulate cellular nucleotide and nucleoside levels. While the nucleoside kinases responsible for the initial phosphorylation of salvaged nucleosides have been well studied, many of the catabolic nucleotidases have only recently been cloned and characterized. Aside from maintaining balanced riboand deoxyribonucleotide pools, substrate cycles that are formed with kinase and nucleotidase activities are also likely to regulate the activation of nucleoside analogues, a class of anticancer and antiviral agents that rely on the nucleoside kinases for phosphorylation to their active forms. Both clinical and in vitro studies suggest that an increase in nucleotidase activity can inhibit nucleoside analogue activation and result in drug resistance. The physiological role of the 5'-nucleotidases will be covered in this review, as will the evidence that these enzymes can mediate resistance to nucleoside analogues. (c) 2005 Published by Elsevier Inc.
引用
收藏
页码:1 / 30
页数:30
相关论文
共 254 条
  • [1] Ahmad I, 2000, CLIN CANCER RES, V6, P1328
  • [2] CD73 engagement promotes lymphocyte binding to endothelial cells via a lymphocyte function-associated antigen-1-dependent mechanism
    Airas, L
    Niemelä, J
    Jalkanen, S
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 165 (10) : 5411 - 5417
  • [3] Differential regulation and function of CD73, a glycosyl-phosphatidylinositol-linked 70-kD adhesion molecule, on lymphocytes and endothelial cells
    Airas, L
    Niemela, J
    Salmi, M
    Puurunen, T
    Smith, DJ
    Jalkanen, S
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 136 (02) : 421 - 431
  • [4] CD73 IS INVOLVED IN LYMPHOCYTE BINDING TO THE ENDOTHELIUM - CHARACTERIZATION OF LYMPHOCYTE VASCULAR ADHESION PROTEIN-2 IDENTIFIES IT AS CD73
    AIRAS, L
    HELLMAN, J
    SALMI, M
    BONO, P
    PUURUNEN, T
    SMITH, DJ
    JALKANEN, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) : 1603 - 1608
  • [5] Bovine cytosolic 5′-nucleotidase acts through the formation of an aspartate 52-phosphoenzyme intermediate
    Allegrin, S
    Sealoni, A
    Ferrara, L
    Pesi, R
    Pinna, P
    Sgarrella, F
    Camici, M
    Eriksson, S
    Tozzi, MG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) : 33526 - 33532
  • [6] Bovine cytosolic IMP/GMP-specific 5'-nucleotidase: cloning and expression of active enzyme in Escherichia coli
    Allegrini, S
    Pesi, R
    Tozzi, MG
    Fiol, CJ
    Johnson, RB
    Eriksson, S
    [J]. BIOCHEMICAL JOURNAL, 1997, 328 : 483 - 487
  • [7] Human erythrocyte pyrimidine 5′-nucleotidase, PN-I, is identical to p36, a protein associated to lupus inclusion formation in response to α-interferon
    Amici, A
    Emanuelli, M
    Raffaelli, N
    Ruggieri, S
    Saccucci, F
    Magni, G
    [J]. BLOOD, 2000, 96 (04) : 1596 - 1598
  • [8] Pyrimidine nucleotidases from human erythrocyte possess phosphotransferase activities specific for pyrimidine nucleotides
    Amici, A
    Emanuelli, M
    Magni, G
    Raffaelli, N
    Ruggieri, S
    [J]. FEBS LETTERS, 1997, 419 (2-3) : 263 - 267
  • [9] Human erythrocyte pyrimidine 5′-nucleotidase, PN-1
    Amici, A
    Magni, G
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 397 (02) : 184 - 190
  • [10] Amici A, 2002, METHOD ENZYMOL, V354, P149