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Association details:
Evidence:
Evidence Level:
Sensitive: D – Preclinical
New
Source:
Title:

A high-throughput screen identifies PARP1/2 inhibitors as a potential therapy for ERCC1-deficient non-small cell lung cancer

Excerpt:
We tested the effect of BMN 673 in our ERCC1-isogenic system and found that ERCC1-deficient clones were significantly more sensitive to BMN 673 than their ERCC1-proficient counterparts (Figure 2f; Supplementary Table S1). Consistent with the enhanced potency of this compound, the ERCC1-selective effect of BMN 673 was achieved at considerably lower concentrations of PARP1/2 inhibitor than for the other clinical inhibitors...