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二氢杨梅素通过STAT3/Bcl-2信号通路促进HNSCC细胞自噬和凋亡

王满英 丁小军 孙扬 余优成

中国临床医学2017,Vol.24Issue(4):571-576,6.
中国临床医学2017,Vol.24Issue(4):571-576,6.DOI:10.12025/j.issn.1008-6358.2017.20160961

二氢杨梅素通过STAT3/Bcl-2信号通路促进HNSCC细胞自噬和凋亡

Dihydromyricetin promotes autophagy and apoptosis in head and neck squamous cell carcinoma cells through STAT3/Bcl-2 signaling pathway

王满英 1丁小军 1孙扬 1余优成1

作者信息

  • 1. 复旦大学附属中山医院口腔科,上海 200032
  • 折叠

摘要

Abstract

Objective:To study the effects of dihydromyricetin(DHM)on cell proliferation and apoptosis of head and neck squamous cell carcinoma(HNSCC).Methods:SCC-25 cancer cells were treated with 12.5,25,50 μmol/L DHM for 6,12,and 24 h.SCC-25 cell apoptosis was detected by flow cytometry.Immunofluorescence was used to observe the emergence of autophagosomes in HNSCC cells.Western blotting was used to detect the expression of apoptosis and autophagy markers in SCC-25.Objective:After treatment of 12.5,25,and 50 μmol/L DHM for 24 h,the apoptosis of SCC-25 cells gradually increased;the apoptotic markers CL-PARP,Bax,and CL-casp3 gradually increased and Bcl-2 gradually decreased(P<0.05).After treatment of 12.5,25,and 50 μmol/L DHM for 24 h,in line with the apoptosis,the autophagy markers of SCC-25 cells gradually changed,the expression of Beclin 1,p62 and the ratio of LC3Ⅱ/LC3Ⅰunderwent changes which were signs of autophagy and the p-STAT3 expression was up-regulated;the ratio of LC3 Ⅱ/LC3 Ⅰ gradually increased,Beclin 1 increased,p62 gradually decreased(P<0.05).Inhibition of autophagy could promote apoptosis of SCC-25 cells which were induced by DHM,increase apoptosis markers CL-PARP and Bax,and decrease Bcl-2(P<0.05).Conclusions:DHM can induce apoptosis and increase autophagy of HNSCC cells.The mechanism is related to STAT3 signaling pathway.Inhibition of autophagy can promote apoptosis of HNSCC cells induced by DHM.

关键词

头颈鳞状细胞癌/二氢杨梅素/凋亡/自噬

Key words

head and neck squamous cell carcinoma/dihydromyricetin/apoptosis/autophagy

分类

医药卫生

引用本文复制引用

王满英,丁小军,孙扬,余优成..二氢杨梅素通过STAT3/Bcl-2信号通路促进HNSCC细胞自噬和凋亡[J].中国临床医学,2017,24(4):571-576,6.

中国临床医学

OACSTPCD

1008-6358

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