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Journal: bioRxiv
Article Title: Depletion of BRCA1 Potentiates Progestin-Induced Cytoskeletal Changes in an Ovarian Cancer Cell Model
doi: 10.64898/2026.01.02.697409
Figure Lengend Snippet: (A) Signaling schematic representing the regulation by PIP5K1C/Rho/ROCK/Rac signaling. (B-I) Average migration of NE-1 and KO-BRCA1 pools in transwell migration assay. Vehicle (ethanol), 10nM R5020, or 10nM R5020 + inhibitor combo treatment for 6-hour migration timepoint, which includes a prior 24-hour pre-treatment of either vehicle (ethanol), 10nM R5020, or 10nM R5020 + inhibitor treatment, respectively. 10% FBS used as chemoattractant. Representative bright-field images to the side of each graph taken at 100µm magnification. (B-C) PIP5K1C Inhibitor: 10µM UNC3230. Graph represents the mean ± SD, * p = 0.0248, ** p ≤ 0.0082, *** p = 0.0001, **** p < 0.0001. (D-E) Rho Inhibitor: 1µg/ml CT04 (Note: no inhibitor pre-treatment). Graph represents the mean ± SD, * p = 0.0285, ** p ≤ 0.0095, **** p < 0.0001. (F-G) ROCK Inhibitor: 10µM Y-27632. Graph represents the mean ± SD, * p ≤ 0.0384, ** p ≤ 0.0016, **** p < 0.0001. (H-1) Rac Inhibitor: 25µM EHT1864. Graph represents the mean ± SD, * p = 0.0120, *** p = 0.0002, **** p < 0.0001.
Article Snippet: Where applicable, cells were treated with the following reagents at the indicated concentrations: 10nM R5020 (Perkin Elmer, NLP004005MG), 10μM UNC3230 (Med Chem Express, HY-110150), 1μg/ml Rho Inhibitor I (Cytoskeleton, Inc, CT04), 10μM Y27632 dihydrochloride (Med Chem Express, HY-10583), and 25μM
Techniques: Migration, Transwell Migration Assay