Skip to main content
Fig. 7 | Cell & Bioscience

Fig. 7

From: MiR-181a targets STING to drive PARP inhibitor resistance in BRCA- mutated triple-negative breast cancer and ovarian cancer

Fig. 7

High miR-181a levels in OvCa FFPE tissues are associated with olaparib resistance. A Quantification of miR-181a levels by RT-qPCR comparing parental and cisplatin- and olaparib-resistant (Resistant) OV81.2 and OV231 cell lines (Student’s t-test). B Quantification of miR-181a levels by RT-qPCR comparing control Clone 1 (CTRL), miR-181a KO Clone 7 (C7), and miR-181a KO Clone 16 (C16) cell lines (One-way ANOVA). C Drug sensitivity assays comparing control Clone 1, miR-181a KO C7, and miR-181a KO C16 cell lines treated with different concentrations of olaparib (One-way ANOVA and Sidak’s multiple comparisons test). *p < 0.05, **p < 0.01, ***p < 0.001. D Representative images of miR-181a ISH in pre-treatment (Pre-Tx) and post-treatment (Post-Tx) paired tissues from OvCa patients. Images of negative control probes (Negative CTRL), positive control probes (Positive CTRL), Pre-Tx, and Post-Tx paired FFPE tissues from OvCa patient #1 (P01). E Quantification of miR-181a levels (dots/nuclei) in Pre-Tx and Post-Tx paired tissues from OvCa patients (Student’s t-test). *p < 0.05, **p < 0.01, ***p < 0.001. Cell viability assays were performed in triplicates. F–I Correlation between miR-181a levels and cisplatin (F), rucaparib (G), olaparib (H), talazoparib (I) drug activity in the BC and OvCa cell lines obtained from CCLE and GDSC BRCA datasets (Pearson’s correlation coefficient)

Back to article page