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Studies on inhibitors of skin tumor promotion, VI. Inhibitory effects of quinones on Epstein-Barr virus activation.

Abstract
To search for possible antitumor promoters, we carried out a primary screening of fifty-one quinones (anthraquinones, naphthoquinones, azaanthraquinones, and azafluorenones) and related compounds, using their possible inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells. Some of these quinones, notably 5-hydroxy-1,2-methylenedioxy-anthraquinone [9], shikonin [29], 2-acetylfuranonaphthoquinone [32], 5,8-dihydroxycleistopholine [37], and 5,8-dihydroxy-2-methyl-1-azaanthraquinone [45], were observed to significantly inhibit the EBV-EA activation at low doses. The position and number of hydroxyl groups on phenyl rings of these quinones affected the inhibitory activity on EBV-EA activation. The investigation indicates that 9, 29, 32, 37, and 45 might be valuable anti-tumor promoters.
AuthorsT Konoshima, M Kozuka, J Koyama, T Okatani, K Tagahara, H Tokuda
JournalJournal of natural products (J Nat Prod) 1989 Sep-Oct Vol. 52 Issue 5 Pg. 987-95 ISSN: 0163-3864 [Print] United States
PMID2558164 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Quinones
  • Tetradecanoylphorbol Acetate
Topics
  • Animals
  • Antineoplastic Agents, Phytogenic (metabolism, pharmacology)
  • Drug Screening Assays, Antitumor
  • Female
  • Herpesvirus 4, Human (drug effects, physiology)
  • Magnetic Resonance Spectroscopy
  • Mice
  • Mice, Inbred ICR
  • Quinones (pharmacology)
  • Structure-Activity Relationship
  • Tetradecanoylphorbol Acetate (metabolism)
  • Tumor Cells, Cultured
  • Virus Activation (drug effects)

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