Repair of DNA damage induced by the novel nucleoside analogue CNDAG through homologous recombination

Cancer Chemother Pharmacol. 2020 Apr;85(4):661-672. doi: 10.1007/s00280-020-04035-x. Epub 2020 Feb 18.

Abstract

Purpose: We postulate that the deoxyguanosine analogue CNDAG [9-(2-C-cyano-2-deoxy-1-β-D-arabino-pentofuranosyl)guanine] likely causes a single-strand break after incorporation into DNA, similar to the action of its cytosine congener CNDAC, and that subsequent DNA replication across the unrepaired nick would generate a double-strand break. This study aimed at identifying cellular responses and repair mechanisms for CNDAG prodrugs, 2-amino-9-(2-C-cyano-2-deoxy-1-β-D-arabino-pentofuranosyl)-6-methoxy purine (6-OMe) and 9-(2-C-cyano-2-deoxy-1-β-D-arabino-pentofuranosyl)-2,6-diaminopurine (6-NH2). Each compound is a substrate for adenosine deaminase, the action of which generates CNDAG.

Methods: Growth inhibition assay, clonogenic survival assay, immunoblotting, and cytogenetic analyses (chromosomal aberrations and sister chromatid exchanges) were used to investigate the impact of CNDAG on cell lines.

Results: The 6-NH2 derivative was selectively potent in T cell malignant cell lines. Both prodrugs caused increased phosphorylation of ATM and its downstream substrates Chk1, Chk2, SMC1, NBS1, and H2AX, indicating activation of ATM-dependent DNA damage response pathways. In contrast, there was no increase in phosphorylation of DNA-PKcs, which participates in repair of double-strand breaks by non-homologous end-joining. Deficiency in ATM, RAD51D, XRCC3, BRCA2, and XPF, but not DNA-PK or p53, conferred significant clonogenic sensitivity to CNDAG or the prodrugs. Moreover, hamster cells lacking XPF acquired remarkably more chromosomal aberrations after incubation for two cell cycle times with CNDAG 6-NH2, compared to the wild type. Furthermore, CNDAG 6-NH2 induced greater levels of sister chromatid exchanges in wild-type cells exposed for two cycles than those for one cycle, consistent with increased double-strand breaks after a second S phase.

Conclusion: CNDAG-induced double-strand breaks are repaired mainly through homologous recombination.

Keywords: ATM signaling pathway; Homologous recombination; Nucleoside analogue; T-ALL; XPF.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Survival
  • Cytarabine / analogs & derivatives*
  • Cytarabine / chemistry
  • Cytarabine / pharmacology
  • DNA Damage / drug effects*
  • DNA Repair / drug effects*
  • Homologous Recombination / drug effects*
  • Humans
  • Leukemia, T-Cell / drug therapy*
  • Leukemia, T-Cell / pathology
  • Phosphorylation
  • Tumor Cells, Cultured

Substances

  • Cytarabine
  • 2'-cyano-2'-deoxyarabinofuranosylcytosine