Related Experiment Video
Updated: Jul 10, 2026

Formation of Covalent DNA Adducts by Enzymatically Activated Carcinogens and Drugs In Vitro and Their Determination by 32P-postlabeling
Published on: March 20, 2018
Investigation in the selective targeting of homologous recombination-deficient cells by benzophenanthridine alkaloid
Yoshihiro Nishida1,2, Takeshi Terabayashi3, Sawako Adachi1
1Department of Obstetrics and Gynecology, Faculty of Medicine, Oita University, Yufu, Oita, 879-5593, Japan.
Abstract:
Homologous recombination (HR) plays a crucial role in maintaining genome integrity in mammalian cells. In this study, a natural product screening indicated that the benzophenanthridine alkaloid nitidine chloride (NC) could selectively kill HR-deficient cells. Mechanistically, this selective cytotoxicity of NC results from the induction of double-strand breaks (DSBs) at DNA replication sites because a single-ended DSB is preferentially repaired by HR. Poly ADP ribose polymerase inhibitors, such as olaparib (OLA), have been developed as HR-targeted drugs. Interestingly, NC treatment resulted in cytotoxic effects in OLA-resistant cells, with an NC/OLA combination treatment showing additive effects on cytotoxicity in HR-deficient cells. With its ability to kill HR-deficient cancer cells, NC has potential as a treatment for hereditary breast and ovary cancer syndrome.
More Related Videos
05:01Assessment of DNA Double Strand Break Repair Activity Using High-throughput and Quantitative Luminescence-Based Reporter Assays
Published on: June 14, 2024
09:29Analysis of Nonhomologous End Joining and Homologous Recombination Efficiency in HEK-293T Cells Using GFP-Based Reporter Systems
Published on: February 2, 2024