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. 2021 Jul 1;49(13):7476–7491. doi: 10.1093/nar/gkab540

Figure 3.

Figure 3.

Loss of CCNC is important for survival and PARPi sensitivity in BRCA2-deficient Cells. (A) Validation of CCNC KO in HEK293A BRCA2 mAID-EGFP KI cells by western blot using the indicated antibodies. (B) Results of long-term clonogenic assays conducted using HEK293A BRCA2 mAID-EGFP CCNC-WT and -KO cells with the indicated treatments. Ola: Olaparib. (C) Quantification of relative cell survival in the clonogenic assays in (B). All treated groups were normalized to the indicated untreated group. The data are presented as means ± SD. ***P < 0.001 (Student's t-test). (D) Results of long-term clonogenic assays conducted using HEK293A BRCA2 mAID-EGFP CCNC-WT and -KO cells with the indicated treatments. Tal: Talazoparib. (E) Quantification of relative cell survival in the clonogenic assays in (D). All treated groups were normalized to the indicated untreated group. The data are presented as means ± SD. ***P < 0.001 (Student's t-test). (F) Capan-1 cells were infected with control pLentiCRISPRv2 (Lenti V2), or CCNC gRNA-1 (g1) virus and selected with puromycin. Western blot was conducted to validate CCNC knock down efficiency with the indicated antibodies. (G) Results of long-term clonogenic assays conducted using Capan-1 LentiV2 and CCNC g1 cells with different concentration of Olaparib treatments. Ola: Olaparib. (H) Quantification of relative cell survival in clonogenic assays in (G). All treated groups were normalized to the indicated untreated group. The data are presented as means ± SD. ***P < 0.001 (Student's t-test). (I) Results of long-term clonogenic assays conducted using Capan-1 LentiV2 and CCNC g1 cells with different concentration of Talazoparib treatments. Tal: Talazoparib. (J) Quantification of relative cell survival in the clonogenic assays in (I). All treated groups were normalized to the indicated untreated group. The data are presented as means ± SD. **P < 0.01, ***P < 0.001 (Student's t-test).