Cited by 24Biochemical and Molecular ResearchAdenosine and Purinergic SignalingGout, Hyperuricemia, Uric Acid

Effect of TEI-6720, a Xanthine Oxidase Inhibitor, on the Nucleoside Transport in the Lung Cancer Cell Line A549

Yamamoto, Tetsuya, Moriwaki, Yuji, Fujimura, Yoshihiro, Takahashi, Sumio, Tsutsumi, Zenta, Tsutsui, Takahiko, Higashino, Kazuya, Hada, Toshikazu·2000·Pharmacology

Abstract

To examine the effect of 2-(3-cyano-4-isobutoxyphenyl)-4-methyl-5-thiazolecarboxylic acid (TEI-6720), an inhibitor of xanthine oxidase, on purine metabolism in the lung cancer cell line A549, the activities of adenosine deaminase, purine nucleoside phosphorylase, adenine phosphoribosyltransferase, hypoxanthine guanine phosphoribosyltransferase, xanthine oxidase, and guanase together with pyrimidine nucleoside phosphorylase were measured with or without the addition of TEI-6720, and the extracellular concentrations of hypoxanthine, xanthine, inosine, uracil, and uridine were measured after the addition of inosine or uridine to the incubation medium with or without TEI-6720. Moreover, the Na-indepenent nucleoside transport was determined in A549 cells with or without TEI-6720. TEI-6720 inhibited the activity of xanthine oxidase in A549 cells, but did not affect other enzymes. During incubation, TEI-6720 not only prevented a decrease in the inosine concentration in inosine-containing medium, but also a decrease in the uridine concentration in uridine-containing medium. Furthermore, the Na-independent transport of uridine was inhibited by TEI-6720 with a K i value of 4.1 μmol/l. These results indicate that TEI-6720 is an inhibitor of the Na-independent nucleoside transport of uridine and inosine, as well as xanthine oxidase.

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Crossref · 10.1159/000028344

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  • Physiological S-nitrosation of specific cysteine residues of RyR2 activates the protein and contributes to maintenance of healthy excitation-contraction coupling.

    “Although the RyR2 contains many surface-exposed thiols, physiological S-nitrosation of specific cysteine residues activate the protein and contribute to maintainance of healthy excitation contraction coupling (1038).”

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Authors
Yamamoto, T., Moriwaki, Y., Fujimura, Y., Takahashi, S., Tsutsumi, Z., Tsutsui, T., Higashino, K., & Hada, T.
Affiliations
  • Hyogo Medical University (JP)
  • Nara Medical University (JP)
Venue
Pharmacology
Publisher
S. Karger AG
Published
2000
Volume
60
Issue
1
Pages
34-40
ISSN
  • 0031-7012 (ISSN-L)
  • 1423-0313
OpenAlex
W2065002260
Cited by
24
References
17
Citations by year
2025: 1 · 2018: 1 · 2015: 2 · 2014: 1 · 2013: 3 · 2012: 3
FWCI
0.12
Type
journal article
Language
en
Open access
closed
Locations
  • Pharmacology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Adenosine and Purinergic Signaling
  • Health Sciences › Medicine › Nephrology › Gout, Hyperuricemia, Uric Acid
Keywords
xanthine oxidase inhibitors, nucleoside transport, Na+-independent transport, uridine transport, purine metabolism, A549 cells, lung cancer, adenosine deaminase, purine nucleoside phosphorylase, adenine phosphoribosyltransferase, hypoxanthine-guanine phosphoribosyltransferase, guanase, pyrimidine nucleoside phosphorylase, inosine, uridine
MeSH terms
Febuxostat, Allopurinol, Biological Transport, Carrier Proteins, Drug Interactions, Enzyme Inhibitors, Humans, Inosine, Lung Neoplasms, Membrane Proteins, Nucleosides, Pentosyltransferases, Purines, Thiazoles, Tumor Cells, Cultured, Uracil, Uridine, Xanthine Oxidase, Hypoxanthine, Xanthine, Nucleoside Transport Proteins, Pyrimidine Phosphorylases

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