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[通过过表达Keap1使Nrf2下调的细胞系H460-N5对抗癌药物的敏感性增加]

[Nrf2 down-regulated cell line H460-N5 with Keap1 over-expression increased sensitivity to anti-cancer drugs].

作者信息

Qu Li-yan, Gao Peng, Wang Hong-yan, Wang Xiu-jun, Tang Xiu-wen

机构信息

Department of Biochemistry and Genetics, College of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2010 Jan;39(1):6-10. doi: 10.3785/j.issn.1008-9292.2010.01.002.

Abstract

OBJECTIVE

To maked a Nrf2 down-regulated cell line by over-expressing Keap1 in H460 cells to study the role of Nrf2 in drug resistance.

METHODS

Transfecting H460 cells with mKeap1-pEGFP and screenig for Keap1 expressing clones by Western blotting with antibodies against Nrf2, HO-1, NQO1 and AKR1C. The cell line with Keap1 over-expression was further confirmed by real-time PCR. The cytotoxicity of H460-N5 to anti-cancer drugs was evaluated by MTS assay.

RESULT

MTS assay results showed the enhanced cytotoxicity of anticancer drugs (Oxaliplatin, Doxorubicin and Etopside) to the H460 cell line with keap1 overexpression compared to the control cell line. In H460-N0 cells, the IC(50) values of Oxaliplation and Etopside were 93 micromol/L and 100 micromol/L respectively whereas the IC(50) values of the two drugs were 42 micromol/L and 30 micromol/L correspondingly in H460-N5 cells. A Nrf2 down-regulated cell line H460-N5 and a control cell line with GFP over-expression have been identified.Down-regulation of Nrf2 enhanced the cytotoxicity of Oxaliplatin, Doxorubicin and Etopside. The IC(50) value of Doxorubicin to H460-N0 cell was above 3 mg/L, but that to H460-N5 cell was about 2 mg/L.

CONCLUSION

A Nrf2 down-regulated cell line H460-N5 and a control cell line with GFP over-expression have been identified. Down-regulation of Nrf2 enhanced the cytotoxicity of Oxaliplatin, Doxorubicin and Etopside.

摘要

目的

通过在H460细胞中过表达Keap1构建Nrf2下调的细胞系,以研究Nrf2在耐药中的作用。

方法

用mKeap1-pEGFP转染H460细胞,并用抗Nrf2、HO-1、NQO1和AKR1C的抗体通过蛋白质印迹法筛选Keap1表达克隆。通过实时PCR进一步确认Keap1过表达的细胞系。通过MTS法评估H460-N5对抗癌药物的细胞毒性。

结果

MTS法结果显示,与对照细胞系相比,抗癌药物(奥沙利铂、阿霉素和依托泊苷)对Keap1过表达的H460细胞系的细胞毒性增强。在H460-N0细胞中,奥沙利铂和依托泊苷的IC(50)值分别为93 μmol/L和100 μmol/L,而在H460-N5细胞中,这两种药物的IC(50)值分别为42 μmol/L和30 μmol/L。已鉴定出Nrf2下调的细胞系H460-N5和GFP过表达的对照细胞系。Nrf2的下调增强了奥沙利铂、阿霉素和依托泊苷的细胞毒性。阿霉素对H460-N0细胞的IC(50)值高于3 mg/L,但对H460-N5细胞的IC(50)值约为2 mg/L。

结论

已鉴定出Nrf2下调的细胞系H460-N5和GFP过表达的对照细胞系。Nrf2的下调增强了奥沙利铂、阿霉素和依托泊苷的细胞毒性。

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