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Isolation and characterisation of a prenylated p-terphenyl metabolite of Aspergillus candidus possessing potent and selective cytotoxic activity; studies on mechanism of action.
Stead, P; Affleck, K; Sidebottom, P J; Taylor, N L; Drake, C S; Todd, M; Jowett, A; Webb, G.
Affiliation
  • Stead P; Bioprocessing Unit, GlaxoWellcome Medicines Research Centre, Stevenage, Herts, UK.
J Antibiot (Tokyo) ; 52(2): 89-95, 1999 Feb.
Article in En | MEDLINE | ID: mdl-10344561
ABSTRACT
We describe the discovery and properties of a prenylated p-terphenyl metabolite of the fungus Aspergillus candidus. The compound (1) possesses potent cytotoxic activity against a range of tumour and other hyper-proliferative cell lines. Cell cycle analysis shows that in mouse keratinocyte (BALB/MK) cells treated with 1, the cell cycle is arrested in early S phase, indicative of an antimetabolite effect. Furthermore, cellular cytotoxicity can be reversed by addition of exogenous pyrimidine but not purine nucleosides to the cell culture medium. It is therefore likely that compound 1 selectively inhibits pyrimidine biosynthesis, and it is this property which accounts for its potent cytotoxic properties.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Terphenyl Compounds / Biphenyl Compounds / Antibiotics, Antineoplastic Limits: Animals Language: En Journal: J Antibiot (Tokyo) Year: 1999 Document type: Article Affiliation country: Reino Unido
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Collection: 01-internacional Database: MEDLINE Main subject: Aspergillus / Terphenyl Compounds / Biphenyl Compounds / Antibiotics, Antineoplastic Limits: Animals Language: En Journal: J Antibiot (Tokyo) Year: 1999 Document type: Article Affiliation country: Reino Unido
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