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CX-5461 is a DNA G-quadruplex stabilizer with selective lethality in BRCA1/2 deficient tumours.
- Source :
-
Nature communications [Nat Commun] 2017 Feb 17; Vol. 8, pp. 14432. Date of Electronic Publication: 2017 Feb 17. - Publication Year :
- 2017
-
Abstract
- G-quadruplex DNAs form four-stranded helical structures and are proposed to play key roles in different cellular processes. Targeting G-quadruplex DNAs for cancer treatment is a very promising prospect. Here, we show that CX-5461 is a G-quadruplex stabilizer, with specific toxicity against BRCA deficiencies in cancer cells and polyclonal patient-derived xenograft models, including tumours resistant to PARP inhibition. Exposure to CX-5461, and its related drug CX-3543, blocks replication forks and induces ssDNA gaps or breaks. The BRCA and NHEJ pathways are required for the repair of CX-5461 and CX-3543-induced DNA damage and failure to do so leads to lethality. These data strengthen the concept of G4 targeting as a therapeutic approach, specifically for targeting HR and NHEJ deficient cancers and other tumours deficient for DNA damage repair. CX-5461 is now in advanced phase I clinical trial for patients with BRCA1/2 deficient tumours (Canadian trial, NCT02719977, opened May 2016).
- Subjects :
- Animals
Base Sequence
Benzoxazines pharmacology
Caenorhabditis elegans drug effects
Cell Line, Tumor
Chromosomal Instability genetics
DNA Damage
DNA Repair drug effects
DNA Replication drug effects
DNA, Ribosomal genetics
Female
Genome, Human
Genotype
Homologous Recombination drug effects
Humans
Mice
Quinolones pharmacology
Saccharomyces cerevisiae metabolism
Transcription, Genetic drug effects
Xenograft Model Antitumor Assays
BRCA1 Protein deficiency
BRCA2 Protein deficiency
Benzothiazoles pharmacology
Benzothiazoles therapeutic use
G-Quadruplexes drug effects
Naphthyridines pharmacology
Naphthyridines therapeutic use
Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 28211448
- Full Text :
- https://doi.org/10.1038/ncomms14432