The critical role of quercetin in autophagy and apoptosis in HeLa cells

被引:42
作者
Wang, Yijun [1 ]
Zhang, Wei [1 ]
Lv, Qiongying [1 ]
Zhang, Juan [1 ]
Zhu, Dingjun [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Gynaecol 1, 238 Jiefang Rd, Wuhan 430060, Hubei Province, Peoples R China
关键词
Quercetin; Autophagy; Apoptosis; Cervical cancer; PROTEIN; GROWTH;
D O I
10.1007/s13277-015-3890-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years, the effects of quercetin on autophagy and apoptosis of cancer cells have been widely reported, while effects on HeLa cells are still unclear. Here, HeLa cells were subjected to quercetin treatment, and then proliferation, apoptosis, and autophagy were evaluated using MTT, flow cytometry, and MDC staining, respectively. The LC3-I/II, Beclin 1, active caspase-3, and S6K1 phosphorylation were detected using Western blot assay. The ultrastructure of HeLa was observed via transmission electron microscope (TEM). Our findings showed that quercetin can dose-dependently inhibit the growth of HeLa cells. The MDC fluorescence was enhanced with increased concentration of quercetin and hit a plateau at 50 mu mol/l. Western blot assay revealed that LC3-I/II ratio, Beclin 1, and active caspase-3 protein were enforced in a dose-dependent method. However, the phosphorylation of S6K1 gradually decreased, concomitant with an increase of autophagy. In addition, TEM revealed that the number of autophagic vacuoles was peaked at 50 mu mol/l of quercetin. Besides, interference of autophagy with 3-MA led to proliferation inhibition and increased apoptosis in HeLa cells, accompanied by the decreased LC3-I/II conversion and the increased active caspase-3. In conclusion, quercetin can inhibit HeLa cell proliferation and induce protective autophagy at low concentrations; thus, 3-MA plus quercetin would suppress autophagy and effectively increased apoptosis.
引用
收藏
页码:925 / 929
页数:5
相关论文
共 15 条
[1]  
BIEDERBICK A, 1995, EUR J CELL BIOL, V66, P3
[2]  
Bogoeva Vanya Petkova, 2014, Sci Pharm, V82, P825, DOI 10.3797/scipharm.1404-09
[3]   Ribosomal protein S6 kinase 1 signaling in prefrontal cortex controls depressive behavior [J].
Dwyer, Jason M. ;
Maldonado-Aviles, Jaime G. ;
Lepack, Ashley E. ;
DiLeone, Ralph J. ;
Duman, Ronald S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (19) :6188-6193
[4]   Regulation of Hypoxia-inducible Factor-1α and Vascular Endothelial Growth Factor Signaling by Plant Flavonoids [J].
Fernando, Wasundara ;
Rupasinghe, H. P. Vasantha ;
Hoskin, David W. .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2015, 15 (06) :479-489
[5]  
Garbar C, 2015, INT J CLIN EXP PATHO, V8, P4344
[6]   Endogenous and exogenous mediators of quercetin bioavailability [J].
Guo, Yi ;
Bruno, Richard S. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2015, 26 (03) :201-210
[7]   Cordycepin induces apoptosis and autophagy in human neuroblastoma SK-N-SH and BE(2)-M17 cells [J].
Li, Yifan ;
Li, Rong ;
Zhu, Shenglang ;
Zhou, Ruyun ;
Wang, Lei ;
Du, Jihui ;
Wang, Yong ;
Zhou, Bei ;
Mai, Liwen .
ONCOLOGY LETTERS, 2015, 9 (06) :2541-2547
[8]   Molecular and physiological actions of quercetin: need for clinical trials to assess its benefits in human disease [J].
Miles, Sarah L. ;
McFarland, Margaret ;
Niles, Richard M. .
NUTRITION REVIEWS, 2014, 72 (11) :720-734
[9]   Naturally occurring products in cancer therapy [J].
Rajesh, E. ;
Sankari, Leena S. ;
Malathi, L. ;
Krupaa, Jayasri R. .
JOURNAL OF PHARMACY AND BIOALLIED SCIENCES, 2015, 7 (05) :S181-S183
[10]   Shikonin promotes autophagy in BXPC-3 human pancreatic cancer cells through the PI3K/Akt signaling pathway [J].
Shi, Shuqing ;
Cao, Haimei .
ONCOLOGY LETTERS, 2014, 8 (03) :1087-1089