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Resveratrol induces human K562 cell apoptosis, erythroid differentiation, and autophagy
被引:17
|作者:
Yan, Hui-Wen
[1
,3
]
Hu, Wei-Xin
[1
]
Zhang, Jie-Ying
[1
]
Wang, Ye
[1
]
Xia, Kun
[2
]
Peng, Min-Yuan
[4
]
Liu, Jing
[1
]
机构:
[1] Cent S Univ, Sch Life Sci, Mol Biol Res Ctr, Changsha 410078, Hunan, Peoples R China
[2] Cent S Univ, State Key Lab Med Genet China, Changsha 410078, Hunan, Peoples R China
[3] Cent S Univ, Sch Life Sci, Dept Cell Biol, Changsha 410078, Hunan, Peoples R China
[4] Cent S Univ, Dept Hematol, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Resveratrol;
K562;
cells;
Apoptosis;
Erythroid differentiation;
Autophagy;
CHRONIC MYELOGENOUS LEUKEMIA;
CHRONIC MYELOID-LEUKEMIA;
CANCER CELLS;
RED WINE;
DISTINCT STAGES;
ERYTHROPOIESIS;
EXPRESSION;
ANTIOXIDANT;
ERYTHROBLASTS;
PHYTOALEXIN;
D O I:
10.1007/s13277-014-1701-y
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Resveratrol (Res) is a naturally occurring phytoalexin with apoptotic and inducing-glob effects in leukemic cells, but the potential induction of erythroid differentiation in cells is not fully understood. Here, we investigated the effects of Res on human erythro-megakaryoblastic leukemia cell line K562. Among the treated cells, proliferation was inhibited and the occurrence of cell apoptosis and cell death were detected. Erythroid differentiation assay was explored, and we found that Res could increase the expression of glycophorin A (GPA), HBA1, HBB, and gamma-globin genes and enforced the expression of GPA, CD71, and Band3 proteins. Res also induced K562 cell autophagy when the concentration of Res was increased up to 50 or 100 mu M. Our findings suggested that Res possesses the potency not only inducing apoptosis but also inducing erythroid differentiation and autophagy in K562 cells. These results provide that Res may be a therapeutic candidate for chronic myelogenous leukemia treatment.
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页码:5381 / 5388
页数:8
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