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[The selective toxic effect of dialdehyde derivatives of the pyrimidine nucleosides on human tumor cells].

Abstract
The impact of a number of synthetic nucleoside derivatives on the growth and survival of cultured human ovarian tumor cells (line SKOV-3) and normal human lung fibroblasts was investigated. It was shown that the dialdehyde derivatives of uridine, 1-β-D-eritrofuranozyl uracil and 3'-O-β-D-ribofuranosyl-2'-deoxythymidine, in contrast to their unoxidized counterparts, exert marked toxic effect on SKOV-3 cells. Cultured human fibroblasts were less susceptible to the damaging effect of the dialdehyde nucleosides. The dialdehyde derivative of 1-β-D-eritrofuranozyl uracil demonstrated greatest differences in the cytotoxic effect on these cultures: inhibition of tumor SKOV-3 cells growth on 50% or more was achieved at the concentrations of this compound ten times lower than in the case of normal fibroblasts.
AuthorsA S Efremova, S I Shram, M S Drenichev, G A Posypanova, N F Myasoedov, S N Mihaylov
JournalBiomeditsinskaia khimiia (Biomed Khim) 2015 Jul-Aug Vol. 61 Issue 4 Pg. 497-502 ISSN: 2310-6972 [Print] Russia (Federation)
PMID26350741 (Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Aldehydes
  • Antineoplastic Agents
  • Cytotoxins
  • Furans
  • Uridine
Topics
  • Aldehydes (chemical synthesis, pharmacology)
  • Antineoplastic Agents (chemical synthesis, pharmacology)
  • Cell Line
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Cytotoxins (chemical synthesis, pharmacology)
  • Female
  • Fibroblasts (cytology, drug effects)
  • Furans (chemical synthesis, pharmacology)
  • Humans
  • Inhibitory Concentration 50
  • Organ Specificity
  • Ovary (drug effects, pathology)
  • Uridine (analogs & derivatives, chemical synthesis, pharmacology)

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