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Time-dependent cytotoxicity induced by SJU-136 (NSC 694501): influence of the rate of interstrand cross-link formation on DNA damage signaling (2006)
  • Arnould,
  • S.,
  • Spanswick,
  • V.J.,
  • Macpherson,
  • J.S.,
  • Hartley,
  • J.A.,
  • Thurston,
  • D.E.,
  • Jodrell,
  • D.I.,
  • Guichard,
  • S.M.

Abstract
Abstract: SJG-136 is a new pyrrolobenzodiazepine dimer inducing time-dependent cytotoxicity. HCT 116 cells were exposed to 50 nmol/L of SJG-136 for 1 hour or 1 nmol/L of SJG-136 for 24 hours to achieve similar levels of interstrand cross-links (ICL). The short exposure led to a rapid formation of ICLs (1 hour), early H2AX foci formation (4 hours), prominent S phase arrest, and greater phosphorylation of Nbs1 (on serine 343) and Chk1 (on serine 317) than a 24-hour exposure. The prolonged exposure at low concentrations of SJG-136 induced a gradual formation of ICLs (up to 24 hours) which was associated with a limited S phase arrest and delayed Nbs1 phosphorylation. Prolonged exposure was also associated with a reduced phosphorylation of p53 on serines 15 and 20, a limited and delayed phosphorylation on serine 392, and a less prominent increase in p21 levels. These data suggest that the 24-hour exposure to a low concentration of SJG-136 led to delayed and reduced DNA damage signaling compared with a higher concentration of SJG-136 for 1 hour, resulting in greater cytotoxicity and contributing to the time-dependent cytotoxic effect of SJG-136.

Publication details
Download http://www.ucl.ac.uk/research/publications/?action=search&pubid=116493
Repository UCL Research Publications Index (MyOPIA) (United Kingdom)
Keywords SPECTRUM ANTITUMOR-ACTIVITY; S-PHASE CHECKPOINT; IN-VIVO; HOMOLOGOUS RECOMBINATION; INDUCED PHOSPHORYLATION; SJG-136 NSC-694501; VERTEBRATE CELLS; MAMMALIAN-CELLS; STRAND BREAKS; DIMER SJG-136
Type JOUR
Relation 1602-1609