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[缺氧诱导因子抑制剂对白血病细胞系中HIF-1α和VEGF表达及凋亡诱导的影响]

[Effects of hypoxia-inducible factor inhibitor on expression of HIF-1alpha and VEGF and induction of apoptosis in leukemic cell lines].

作者信息

Wang Fei, Chen Bao-An, Cheng Jian, Xu Wen-Lin, Wang Xue-Mei, Ding Jia-Hua, Gao Chong, Sun Yun-Yu, Wang Jun, Zhao Gang, Bao Wen, Song Hui-Hui, Gao Feng, Zhang Wei, Xia Guo-Hua, Pei Xiao-Ping, Wu Wei-Wei, Yin Li, Shan Xue-Yun

机构信息

Department of Hematology, Zhongda Hospital, Southeast University Clinical Medical College, Nanjing 210009, Jiangsu Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Feb;18(1):74-8.


DOI:
PMID:20137122
Abstract

This study was purposed to investigate the effect of a hypoxia-inducible factor inhibitor (YC-1) on expression of hypoxia-inducible factor 1alpha (HIF-1alpha) and vascular endothelial growth factor (VEGF) as well as induction of apoptosis in leukemic cell lines. RT-PCR was used to determine the levels of HIF-1alpha mRNA and VEGF mRNA in K562, U937 and Jurkat cells. After treatment of U937 cell with 4 micromol/L YC-1, cell apoptosis was assayed by DAPI staining under fluorescent microscope and flow cytometry with Annexin V-FITC/PI staining; the expression levels of HIF-1alpha mRNA and VEGF mRNA were measured with RT-PCR; the expression levels of HIF-1alpha, VEGF, BAX, BCL-2 and caspase-3 proteins were measured by Western blot. The results showed that HIF-1alpha mRNA and VEGF mRNA were expressed in all three leukemia cell lines. After treatment of U937 cell with 4 micromol/L YC-1 for 0, 8, 16 and 24 hours, the changes of morphologic features of U937 cells could be observed under fluorescent microscope and the apoptotic rates significantly increased in time-dependent manner, they were (4.87 +/- 0.70)%, (27.27 +/- 2.00)%, (51.53 +/- 2.81) and (60.5 +/- 3.20)% respectively, the expression levels of VEGF mRNA reduced, while the expression levels of HIF-1alpha mRNA had no obviously changes.Furthermore, the expression of HIF-1alpha, VEGF and BCL-2 decreased, while the expression of BAX and caspase-3 increased, the ratio of BAX/BCL-2 increased in time-dependent manner (r = 0.973, p < 0.01). It is concluded that HIF-1alpha mRNA and VEGF mRNA are all expressed in in K562, U937 and Jurkat cells, YC-1 has significant effect on down-regulating the protein expression of HIF-1alpha and VEGF, and induces the apoptosis in U937. The mechanism of apoptosis in leukemic cells may involve in up-regulating BAX/BCL-2 ratio and expression of protein caspase-3.

摘要

本研究旨在探讨缺氧诱导因子抑制剂(YC-1)对白血病细胞系中缺氧诱导因子1α(HIF-1α)和血管内皮生长因子(VEGF)表达以及细胞凋亡诱导的影响。采用逆转录聚合酶链反应(RT-PCR)检测K562、U937和Jurkat细胞中HIF-1α mRNA和VEGF mRNA水平。用4 μmol/L YC-1处理U937细胞后,通过荧光显微镜下DAPI染色和Annexin V-FITC/PI染色的流式细胞术检测细胞凋亡;用RT-PCR检测HIF-1α mRNA和VEGF mRNA表达水平;用蛋白质免疫印迹法检测HIF-1α、VEGF、BAX、BCL-2和caspase-3蛋白表达水平。结果显示,三种白血病细胞系均表达HIF-1α mRNA和VEGF mRNA。用4 μmol/L YC-1处理U937细胞0、8、16和24小时后,荧光显微镜下可观察到U937细胞形态特征的变化,凋亡率呈时间依赖性显著增加,分别为(4.87±0.70)%、(27.27±2.00)%、(51.53±2.81)%和(60.5±3.20)%,VEGF mRNA表达水平降低,而HIF-1α mRNA表达水平无明显变化。此外,HIF-1α、VEGF和BCL-2表达降低,而BAX和caspase-3表达增加,BAX/BCL-2比值呈时间依赖性增加(r = 0.973,p < 0.01)。结论:K562、U937和Jurkat细胞均表达HIF-1α mRNA和VEGF mRNA,YC-1对下调HIF-1α和VEGF蛋白表达有显著作用,并诱导U937细胞凋亡。白血病细胞凋亡机制可能与上调BAX/BCL-2比值和caspase-3蛋白表达有关。

相似文献

[1]
[Effects of hypoxia-inducible factor inhibitor on expression of HIF-1alpha and VEGF and induction of apoptosis in leukemic cell lines].

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010-2

[2]
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Urol Int. 2012

[3]
Effects of YC-1 on hypoxia-inducible factor 1-driven transcription activity, cell proliferative vitality, and apoptosis in hypoxic human pancreatic cancer cells.

Pancreas. 2007-3

[4]
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Mol Vis. 2013

[5]
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[6]
[Inhibitory effect of YC-1 on induction of VEGF and GPI genes in hypoxic human pancreatic cancer cells].

Zhonghua Zhong Liu Za Zhi. 2006-7

[7]
Hypoxic stress simultaneously stimulates vascular endothelial growth factor via hypoxia-inducible factor-1α and inhibits stromal cell-derived factor-1 in human endometrial stromal cells.

Hum Reprod. 2011-11-28

[8]
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Ann Clin Lab Sci. 2014

[9]
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Cardiovasc J Afr. 2010

[10]
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Exp Eye Res. 2009-7-4

引用本文的文献

[1]
YC-1 induces G/G phase arrest and mitochondria-dependent apoptosis in cisplatin-resistant human oral cancer CAR cells.

Biomedicine (Taipei). 2017-6

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