OncoTargets and Therapy · 2020 · 15 citations · 19 references
MedicineOncologyPharmacologyCancer PharmacologyCell SignalingMolecular OncologyBreast Cancer PharmacotherapyCancer Cell SignalingCell-cycle DysregulationMitotic InhibitorsSignal Transduction In CancerBreast Cancer PrognosisCancer Cell Proliferation InhibitionCell Cycle Arrest MechanismsCell Cycle InhibitionG1 Cell-cycle ArrestWnt Signal TransductionWnt Signaling In ProliferationWnt Signaling Modulation
Background: Breast cancer exhibits poor prognosis and high relapse rates following chemotherapy therapeutics. Thus, this study aims to develop effective novel agents regulating the core molecular pathway of breast cancer such as Wnt/β-catenin signaling. Methods: The present study screened a novel inhibitor, called “C188”, using MTT assay. The molecular formula of C188 is C 21 H 15 FN 4 O 3 and the molecular weight is 390. Flow cytometry and Western blotting were employed to assess cell cycle arrest after treatment with C188. Wound-healing and transwell assays were applied to measure the cell migration and invasion viability. The regulatory effects of C188 on Wnt/β‑catenin signaling and localization of β‑catenin in the nucleus were investigated by Western blotting and immunofluorescence. Results: We found that C188 significantly suppressed proliferation and growth in a dose- and time-dependent manner in breast cancer cells, but not in normal breast cells. The inhibitory effect was caused by cell cycle arrest at the G1-phase which is induced by C188 treatment. Additionally, C188 dramatically inhibited cell migration of breast cancer cells in a dose-dependent manner. The migration inhibition was attributed to the suppression of Wnt/β‑catenin signaling and localization of β‑catenin in the nucleus mediated by regulating phosphorylation of β‑catenin and its subsequent stability. Furthermore, the target genes, including Axin 2 , c-JUN , and c-Myc , were downregulated due to the decrease of β‑catenin in the nucleus after exposure to C188. Conclusion: C188 treatment resulted in the downregulation of cyclin D which led to cell cycle arrest at the G1 phase, and the inhibition of cell migration, indicating that C188 may be an effective novel therapeutic candidate as a potential treatment for human breast cancer. Keywords: C188, breast cancer, proliferation, cell cycle, cell migration, Wnt/β-catenin
19
β-Catenin regulates expression of cyclin D1 in colon carcinoma cells
Osamu Tetsu, Frank McCormick · Nature · 1999 · 3.6K citations
Medicine, Cell Biology, Oncology +14
Paul Polakis · Genes & Development · 2000 · 3.2K citations · Full text
Wnt Signaling through Inhibition of β-Catenin Degradation in an Intact Axin1 Complex
Vivian Li, Ser Sue Ng, Paul J. Boersema et al. · Cell · 2012 · 903 citations · Full text