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[2-甲氧基雌二醇与三氧化二砷对骨髓瘤细胞凋亡相关基因表达谱的影响研究]

[Investigation of the effect of 2-methoxyestradiol and arsenic trioxide on the apoptosis-associated gene expression profile of myeloma cells].

作者信息

Xiong Hong, Hou Jian, Gao Wei-Ran, Chen Qu-Bo

机构信息

Department of Hematology, Changzheng Hospital, Second Military Medical College, Shanghai 200003, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2005 Apr;26(4):200-4.

PMID:15949259
Abstract

OBJECTIVE

To explore the effect of 2-methoxyestradiol (2ME2) and arsenic trioxide (As2O3) on the apoptosis related gene expression in multiple myeloma cell line CZ-1.

METHODS

Total RNA was isolated from CZ-1 cells which had been treated with 2ME2 and As2O3 at an apoptosis-inducing concentration and reverse-transcribed into a cDNA probe labeled with Bio-16-dUTP, and then hybridized it with a microarray containing up to 96 key genes involved in apoptosis. The gene expression profile of the 2ME2 and As2O3 treated CZ-1 cells were analyzed with GEArray Analyzer software. The microarray results were confirmed by RT-PCR.

RESULTS

As2O3 treatment caused the alteration in the expression of 52 genes (54.2% of total genes on microarray). Among them, 42 (80.8%) were upregulated and 10 (19.2%) were downregulated. The upregulated genes were mainly involved in caspases family, P53 and ATM pathway, death effector domain family, TNF receptor family and CIDE family. 2ME2 treatment resulted in the alteration of 42 genes (43.8% of the total genes on microarray). Of them, 32 (76.2%) were downregulated and 10 (23.8%) were upregulated. The downregulated genes mainly belonged to bcl-2 family, inhibitor of apoptosis protein family (IAP), TRAF family, TNF ligand family, and CARD family.

CONCLUSION

2ME2 and As2O3 induce the CZ-1 cells apoptosis by different pathways. As2O3 mainly induces upregulation of proapoptotic genes, and 2ME2 downregulation of anti-apoptotic genes expression.

摘要

目的

探讨2-甲氧基雌二醇(2ME2)和三氧化二砷(As2O3)对多发性骨髓瘤细胞系CZ-1中凋亡相关基因表达的影响。

方法

从经凋亡诱导浓度的2ME2和As2O3处理的CZ-1细胞中提取总RNA,逆转录成用Bio-16-dUTP标记的cDNA探针,然后与包含多达96个参与凋亡的关键基因的微阵列杂交。用GEArray Analyzer软件分析2ME2和As2O3处理的CZ-1细胞的基因表达谱。微阵列结果通过RT-PCR进行验证。

结果

As2O3处理导致52个基因(占微阵列上总基因的54.2%)表达改变。其中,42个(80.8%)上调,10个(19.2%)下调。上调的基因主要涉及半胱天冬酶家族、P53和ATM途径、死亡效应结构域家族、肿瘤坏死因子受体家族和CIDE家族。2ME2处理导致42个基因(占微阵列上总基因的43.8%)表达改变。其中,32个(76.2%)下调,10个(23.8%)上调。下调的基因主要属于bcl-2家族、凋亡抑制蛋白家族(IAP)、TRAF家族、肿瘤坏死因子配体家族和CARD家族。

结论

2ME2和As2O3通过不同途径诱导CZ-1细胞凋亡。As2O3主要诱导促凋亡基因上调,而2ME2下调抗凋亡基因表达。

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