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©The Author(s) 2023.
World J Gastrointest Oncol. Feb 15, 2023; 15(2): 332-342
Published online Feb 15, 2023. doi: 10.4251/wjgo.v15.i2.332
Published online Feb 15, 2023. doi: 10.4251/wjgo.v15.i2.332
Figure 1 JAB-8263 dose-dependently suppressed colorectal cancer cell proliferation and colony formation in vitro.
A: Human colorectal cancer cell lines including HT29, DLD1, Colo205, H716, SW837 and H508 were treated with JAB-8263 for 6 d, and the proliferation was dose-dependently suppressed; B: The MC38 mouse cell line was treated with JAB-8263 for 6 d, and the proliferation was dose-dependently suppressed; C: The IC50 values of HT-29, DLD-1, Colo205, H716, SW837, H508 and MC38 were 0.15, 1.24, 0.19, 0.09, 0.57, 0.14 and 1.25 μmol/L. Colony formation assays for six colorectal cancer cell lines including MC38, HT29, H508, SW837 and DLD1 were treated with various concentrations of JAB-8263 for 5 d. Cell proliferation in all cell lines was dose-dependently suppressed. All experiments were performed in triplicate. Conc.: Concentration.
- Citation: Liu XM, Xia SY, Long W, Li HJ, Yang GQ, Sun W, Li SY, Du XH. Potent bromodomain and extraterminal domain inhibitor JAB-8263 suppresses MYC expression and exerts anti-tumor activity in colorectal cancer models. World J Gastrointest Oncol 2023; 15(2): 332-342
- URL: https://www.wjgnet.com/1948-5204/full/v15/i2/332.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v15.i2.332