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©The Author(s) 2023.
World J Gastrointest Oncol. Oct 15, 2023; 15(10): 1756-1770
Published online Oct 15, 2023. doi: 10.4251/wjgo.v15.i10.1756
Published online Oct 15, 2023. doi: 10.4251/wjgo.v15.i10.1756
Figure 1 The effects of pomolic acid and pomolic acid-28-O-β-D-glucopyranosyl ester on proliferation of colon cancer cells.
A: The proliferation of HT-29 cells after treatment with different concentrations of pomolic acid (PA) for 24, 48, and 72 h; B: The proliferation of HT-29 cells after treatment with different concentrations of pomolic acid-28-O-β-D-glucopyranosyl ester (PAO) for 24, 48, and 72 h; C: The cell cycle distribution of HT-29 cells after treatment with different concentrations of PA for 24 h; D: The cell cycle distribution of HT-29 cells after treatment with different concentrations of PA for 48 h; E: The cell cycle distribution of HT-29 cells after treatment with different concentrations of PAO for 24 h; F: The cell cycle distribution of HT-29 cells after treatment with different concentrations of PAO for 48 h. aP < 0.05, bP < 0.01, cP < 0.001, dP < 0.0001.
- Citation: Liu LY, Yu TH, Liao TS, Xu P, Wang Y, Shi M, Li B. Pomolic acid and its glucopyranose ester promote apoptosis through autophagy in HT-29 colon cancer cells. World J Gastrointest Oncol 2023; 15(10): 1756-1770
- URL: https://www.wjgnet.com/1948-5204/full/v15/i10/1756.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v15.i10.1756