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- W1181191570 abstract "3302 The pyrrolobenzodiazepines (PBDs) are a family of naturally occurring antitumor antibiotics. Many of the most potent family members contain a C2-endo-exo unsaturated motif associated with the pyrrolo C-ring of the PBD. SG2202 is a PBD dimer consisting of two PBD monomer units, which retain the endo-exo unsaturation motif in the form of a C2-aryl substituent conjugated to a 2,3 double bond, joined via their C8/C8’ positions through a propyldioxy linker. SG2285 is a prodrug of SG2202 whereby two bisulphite groups inactivate the N10-C11 imines of the PBD units. Once the bisulphite groups are eliminated to produce SG2202 the two PBD imine moieties are able to bind covalently in the minor groove of DNA to the N2-positions of guanine on opposite strands of DNA to form an interstrand crosslink (ICL). SG2285 is highly potent in vitro, with sub-nM GI50 values in most human tumour cell lines tested using the Alamar blue assay following continuous exposure. A modification of the single cell gel electrophoresis (comet) assay has shown SG2285 to be highly efficient at producing ICLs in cells, which form more slowly than those produced by SG2202. Using DNA repair-deficient cell lines cellular sensitivity to SG2285 was shown to be dependent on the ERCC1/XPF heterodimer and homologous recombination. In 20 primary chronic lymphocytic leukaemia (B-CLL) samples the mean LD50 value (Annexin V / propidium iodide assay) was 8.3(±3.4) nM. Although there was a trend towards increased resistance to SG2285 in cells from previously treated (n=10) compared to untreated (n=10) patients this did not reach significance (p=0.07). LD50 values in normal age-matched B- and T-lymphocytes were significantly higher (p" @default.
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- W1181191570 date "2008-05-01" @default.
- W1181191570 modified "2023-09-27" @default.
- W1181191570 title "SG2285, a novel C2-aryl-substituted pyrrolobenzodiazepine dimer prodrug with potent antitumor activity" @default.
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