Effects of Juglandis Immaturum ExocarpiumPolysaccharide on Proliferation, Apoptosis and PI3K/Akt Signaling Pathway of Human Colon Carcinoma Cell Line HCT-116
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Effects of Juglandis Immaturum ExocarpiumPolysaccharide on Proliferation, Apoptosis and PI3K/Akt Signaling Pathway of Human Colon Carcinoma Cell Line HCT-116
Chinese Journal of Experimental Traditional Medical FormulaeVol. 22, Issue 18, Pages: 136-139(2016)
HU Ze-cheng. Effects of Juglandis Immaturum ExocarpiumPolysaccharide on Proliferation, Apoptosis and PI3K/Akt Signaling Pathway of Human Colon Carcinoma Cell Line HCT-116[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(18): 136-139.
DOI:
HU Ze-cheng. Effects of Juglandis Immaturum ExocarpiumPolysaccharide on Proliferation, Apoptosis and PI3K/Akt Signaling Pathway of Human Colon Carcinoma Cell Line HCT-116[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(18): 136-139. DOI: 10.13422/j.cnki.syfjx.2016180136.
Effects of Juglandis Immaturum ExocarpiumPolysaccharide on Proliferation, Apoptosis and PI3K/Akt Signaling Pathway of Human Colon Carcinoma Cell Line HCT-116
Objective: To explore the effects of Juglandis Immaturum Exocarpium polysaccharide(JIP) on the proliferation
apoptosis and phosphatidylinositol 3'-OH kinase/protein kinase B(PI3K/Akt) signaling pathway of human colon carcinoma cell line HCT-116. Method: The HCT-116 cells in logarithmic growth phase were treated with JIP(10
20
50
100 mg·L-1)
and another blank group was set up. The inhibition rates of proliferation at 24
48
72
96 h post-treatment were measured by MTS assay. The cell cycle and apoptosis rate at 48 h post-treatment were detected by PI single staining and Annexin-FITC/PI double staining methods
and the protein levels of Akt and p-Akt at 48 h post-treatment were detected by Western blot assay. Result: JIP presented significant inhibitory effect on HCT-116 cell proliferation in a dose-and time-dependent manner. As compared with the blank group
the cells ratio in G0/G1 phase was increased and cells ratio in S phase and G2/M phase was declined with significant differences in various groups(P<0.05). As compared with the blank group
the early apoptosis rate of JIP in all the groups except 10 mg·L-1 group was significantly increased
and the apoptosis rate of late phase and total apoptosis rate in various groups were significantly increased with statistical significance(P<0.05). As compared with the blank group
the ratio of p-Akt/Akt was decreased in various treatment groups
and there was statistically significant difference in ratio of p-Akt/Akt between various concentrations(P<0.05). Conclusion: JIP can directly inhibit or kill human colon cells HCT-116 cellsin vitro
and present ability to inhibit proliferation and induce apoptosis. The mechanism might associated with PI3K/Akt signaling pathway.
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