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转录因子 Sp1 和 Sp3 调节人 ABCG2 基因的表达和化疗耐药表型。

Transcription factors Sp1 and Sp3 regulate expression of human ABCG2 gene and chemoresistance phenotype.

机构信息

Department of Environmental Medical Biology, Institute of Tropical Medicine, and Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, 120-752, Korea.

出版信息

Mol Cells. 2013 Oct;36(4):368-75. doi: 10.1007/s10059-013-0191-x. Epub 2013 Aug 29.

Abstract

ABCG2 is a member of the ATP binding cassette (ABC) transmembrane proteins that plays an important role in stem cell biology and drug resistance of cancer cells. In this study, we investigated how expression of human ABCG2 gene is regulated in lung cancer A549 cells. Binding of Sp1 and Sp3 transcription factors to the ABCG2 promoter in vitro and in vivo was elucidated by electrophoretic mobility shift assay and chromatin immunoprecipitation assay. The ABCG2 promoter activity was impaired when Sp1 sites were mutated but was enhanced by overexpression of Sp1 or Sp3 proteins. Knockdown of Sp1 or Sp3 expression by short interfering RNA significantly decreased the expression of ABCG2 mRNA and protein, resulting in attenuated formation of the side population in A549 cells. In addition, Sp1 inhibition in vivo by mithramycin A suppressed the percentage of the side population fraction and sphere forming activities of A549 cells. Moreover, inhibiting Sp1- or Sp3-dependent ABCG2 expression caused chemosensitization to the anticancer drug cisplatin. Collectively, our results demonstrate that Sp1 and Sp3 transcription factors are the primary determinants for activating basal transcription of the ABCG2 gene and play an important role in maintaining the side population phenotype of lung cancer cells.

摘要

ABCG2 是 ATP 结合盒(ABC)跨膜蛋白家族的一员,在干细胞生物学和癌细胞的耐药性中发挥重要作用。在本研究中,我们研究了人 ABCG2 基因在肺癌 A549 细胞中的表达是如何调控的。通过电泳迁移率变动分析和染色质免疫沉淀分析,阐明了 Sp1 和 Sp3 转录因子在体外和体内与 ABCG2 启动子的结合。当 Sp1 结合位点发生突变时,ABCG2 启动子活性受损,但 Sp1 或 Sp3 蛋白的过表达增强了其活性。用短发夹 RNA 敲低 Sp1 或 Sp3 的表达,显著降低了 ABCG2 mRNA 和蛋白的表达,导致 A549 细胞侧群的形成减少。此外,米托蒽醌 A 体内抑制 Sp1 可抑制 A549 细胞侧群分数和球体形成活性的百分比。此外,抑制 Sp1 或 Sp3 依赖性 ABCG2 表达可导致顺铂等抗癌药物的化疗敏感性增加。综上所述,我们的研究结果表明,Sp1 和 Sp3 转录因子是激活 ABCG2 基因基础转录的主要决定因素,并在维持肺癌细胞侧群表型中发挥重要作用。

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