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首页> 外文期刊>Biochemical and Biophysical Research Communications >Ets1 promotes chemoresistance and invasion of paclitaxel-resistant, hormone-refractory pc3 prostate cancer cells by up-regulating mdr1 and mmp9 expression
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Ets1 promotes chemoresistance and invasion of paclitaxel-resistant, hormone-refractory pc3 prostate cancer cells by up-regulating mdr1 and mmp9 expression

机译:ETS1通过UP调节MDR1和MMP9表达促进紫杉醇抗性,激素难治性PC3前列腺癌细胞的化学抑制和侵袭

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摘要

ETS1, which belongs to the ETS transcription factor family, plays important roles in diverse aspects of cancer such as drug resistance and metastasis. In the present study, we examined the functional roles of ETS1 in paclitaxel resistance and invasion using human prostate cancer PC3cells and paclitaxel-resistant PC3PR cells established from PC3 cells. Our results showed that ETS1mRNA and protein expression was markedly up-regulated in paclitaxel-resistant PC3PR cells compared with paclitaxel-sensitive PC3 cells. The mRNA levels of MDR1 as well as MMP1, MMP3, MMP9 and uPA were positively correlated with that of ETS1. In PC3PR cells, silencing of ETS1 expression by siRNAs inhibited the activity of the MDR1 promoter containing ETS binding sites, reduced the mRNA and protein levels of MDR1 and suppressed paclitaxel resistance. Furthermore, ETS1 knockdown decreased secretion of MMP9 as well as its intracellular mRNA level, and dramatically inhibited invasion of PC3PR cells. Our results suggest that ETS1 promotes paclitaxel resistance and invasion in part by up-regulating MDR1 and MMP9 expression. Taken together, a novel therapeutic strategy targeting the ETS1 gene could be designed to overcome chemoresistance and metastasis of taxane-resistant, hormone-refractory prostate cancer.
机译:ETS1属于ETS转录因子家族,在癌症等多种方面起重要作用,例如耐药性和转移。在本研究中,我们研究了ETS1在PACLitaxel抗性和侵袭中使用人的前列腺癌PC3Cells和从PC3细胞建立的紫杉醇抗性PC3PR细胞的侵袭的功能作用。我们的结果表明,与紫杉醇敏感的PC3细胞相比,ETS1MRNA和蛋白表达在紫杉醇抗性PC3PR细胞中明显上调。 MDR1以及MMP1,MMP3,MMP9和UPA的mRNA水平与ETE1的MMP1,MMP3,MMP9和UPA呈正相关。在PC3PR细胞中,SIRNA的ETS1表达的沉默抑制了含有ETS结合位点的MDR1启动子的活性,降低了MDR1的mRNA和蛋白质水平并抑制了紫杉醇抗性。此外,ETS1敲低降低了MMP9的分泌以及其细胞内mRNA水平,并显着抑制了PC3PR细胞的侵袭。我们的研究结果表明,ETS1促进了紫杉醇抗性和侵袭部分,部分地通过上调MDR1和MMP9表达。占据了靶向ETS1基因的新型治疗策略,可以设计用于克服紫杉烷抗性激素难治性前列腺癌的化学化和转移。

著录项

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  • 作者单位

    Department of Urology Gifu University Graduate School of Medicine 1-1 Yanagido Gifu 501-1193;

    Department of Longevity and Aging Research Gifu International Institute of Biotechnology 1-1 Naka;

    Department of Urology Gifu University Graduate School of Medicine 1-1 Yanagido Gifu 501-1193;

    Research Equipment Center Hamamatsu University School of Medicine Hamamatsu Shizuoka 431-3192;

    Department of Longevity and Aging Research Gifu International Institute of Biotechnology 1-1 Naka;

    Department of Urology Gifu University Graduate School of Medicine 1-1 Yanagido Gifu 501-1193;

    Department of Longevity and Aging Research Gifu International Institute of Biotechnology 1-1 Naka;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    ETS1; MDR1; Metastasis; MMP9; Paclitaxel resistance; Prostate cancer;

    机译:ETS1;MDR1;转移;MMP9;紫杉醇抗性;前列腺癌;

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