http://cancerres.aacrjournals.org/content/73/24_Supplement/P2-09-02#:~:text=Response%20in%20Germline%20BRCA%20Patients.%20Conclusions%3A%20BMN%20673,side%20effects%20associated%20with%20need%20for%20dose%20reduction. WebAug 7, 2015 · Our data indicate that BMN 673 has anti-proliferative and pro-apoptotic effects on a Brca1 -deficient murine ovarian cancer cell line. ID8-Vegf cells, which are Brca1 wild type, are unaffected by BMN 673 treatment, confirming that the drug is an on-target PARP1 inhibitor. The synthetic lethal phenotype can be observed in any cell that exhibits
BMN-673 Embraca Study (Talazoparib) - Advanced breast …
WebJul 1, 2024 · Abstract. Inhibition of poly (ADP-ribose) polymerase (PARP) sensitizes tumor cells to DNA damage that would normally be repaired through the base excision repair pathway. PARP inhibitors are active clinically against BRCA-deficient ovarian cancers. The PARP inhibitor talazoparib produces cytotoxicity in human cancer cell lines and animal … WebTalazoparib (BMN 673, LT-673) is a novel PARP inhibitor with IC50 of 0.57 nM for PARP1 in a cell-free assay. It is also a potent inhibitor of PARP-2, but does not inhibit PARG and is … tobe childers charlotte
Abstract 4678: Pilot trial of talazoparib (BMN 673), an oral PARP ...
WebOct 22, 2013 · An investigational new PARP inhibitor, BMN 673, is showing early responses in patients with heavily pretreated, advanced, BRCA-related cancers of the breast and … WebNov 21, 2013 · BMN 673 has been shown to cause single-agent synthetic lethality in breast cancer 1 and breast cancer 2 (BRCA1/2)- and phosphatase and tensin homolog (PTEN)-deficient cell lines and has potent antitumor activity in animal models of tumors harboring mutations in DNA repair pathways. WebNov 21, 2013 · The effects of BMN 673 on the developing human fetus are unknown. For this reason and because PARP inhibitors are known to be teratogenic, women of … penn state michigan tv coverage