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©The Author(s) 2024.
World J Gastrointest Oncol. Nov 15, 2024; 16(11): 4456-4467
Published online Nov 15, 2024. doi: 10.4251/wjgo.v16.i11.4456
Published online Nov 15, 2024. doi: 10.4251/wjgo.v16.i11.4456
Figure 7 Notch 1 is involved in the inhibitory effect of dioscin on HCT116.
HCT116 cells were treated with dioscin (5 μg/mL), Jagged 1 (5 μg/mL), dioscin (2.5 μg/mL) + Jagged 1 (5 μg/mL) for 48 hours. A: Apoptosis in HCT116 cells was revealed using flow cytometry as well as annexin V-FITC as well as PI staining methods; B: Quantification of apoptosis in HCT116 cells from flow cytometry results; C: RT qPCR analysis was performed using caspase-3 mRNA expression and Bax/Bcl-2 ratio; D: Expression levels of Bax, Bcl-2, as well as other proteins were detected using Western blot analysis; E: Quantification of Bax, Bcl-2, and other protein expression levels from the Western blot analysis; F: Transwell method was used to detect the level of inhibition of HCT116 cell invasion; G: Quantification of HCT116 cell invasion inhibition following dioscin treatment using the Transwell assay; H: Wound healing assay was used to detect the inhibition of HCT116 cell migration; I: Quantification of HCT116 cell migration inhibition following treatment using the wound healing assay. Three biological repeats were used and reported as mean ± SD. aP < 0.05, bP < 0.01, cP < 0.001 compare to the control group, dP < 0.05, eP < 0.01, fP < 0.01 compare to the dioscin group.
- Citation: Cai XX, Huang ZF, Tu FY, Yu J. Impact and mechanism study of dioscin on biological characteristics of colorectal cancer cells. World J Gastrointest Oncol 2024; 16(11): 4456-4467
- URL: https://www.wjgnet.com/1948-5204/full/v16/i11/4456.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v16.i11.4456