Resumen
The homologous recombination (HR) pathway plays a crucial role in the repair of DNA double-strand breaks (DSBs) and interstrand cross-links (ICLs). RAD51, a key protein of HR, possesses a unique activity: DNA strand exchange between homologous DNA sequences. Recently, using a high-throughput screening (HTS), we identified compound 1 (B02), which specifically inhibits the DNA strand exchange activity of human RAD51. Here, we analyzed the mechanism of inhibition and found that 1 disrupts RAD51 binding to DNA. We then examined the effect of 1 on HR and DNA repair in the cell. The results show that 1 inhibits HR and increases cell sensitivity to DNA damage. We propose to use 1 for analysis of cellular functions of RAD51. Because DSB- and ICL-inducing agents are commonly used in anticancer therapy, specific inhibitors of RAD51 may also help to increase killing of cancer cells.
Idioma original | English (US) |
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Páginas (desde-hasta) | 3011-3020 |
Número de páginas | 10 |
Publicación | Journal of Medicinal Chemistry |
Volumen | 55 |
N.º | 7 |
DOI | |
Estado | Published - abr 12 2012 |
Publicado de forma externa | Sí |
ASJC Scopus subject areas
- Drug Discovery
- Molecular Medicine