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表观遗传因子KDM2B调控结肠肿瘤细胞中的上皮-间质转化及小GTP酶

The Epigenetic Factor KDM2B Regulates EMT and Small GTPases in Colon Tumor Cells.

作者信息

Zacharopoulou Nefeli, Tsapara Anna, Kallergi Galatea, Schmid Evi, Alkahtani Saad, Alarifi Saud, Tsichlis Philip N, Kampranis Sotirios C, Stournaras Christos

机构信息

Department of Biochemistry, University of Crete Medical School, Voutes, Heraklion, Greece.

Department of Pediatric Surgery & Pediatric Urology, Children's Hospital, Eberhard-Karls-University Tuebingen, Tuebingen, Germany.

出版信息

Cell Physiol Biochem. 2018;47(1):368-377. doi: 10.1159/000489917. Epub 2018 May 14.

Abstract

BACKGROUND/AIMS: The epigenetic factor KDM2B is a histone demethylase expressed in various tumors. Recently, we have shown that KDM2B regulates actin cytoskeleton organization, small Rho GTPases signaling, cell-cell adhesion and migration of prostate tumor cells. In the present study, we addressed its role in regulating EMT and small GTPases expression in colon tumor cells.

METHODS

We used RT-PCR for the transcriptional analysis of various genes, Western blotting for the assessment of protein expression and immunofluorescence microscopy for visualization of fluorescently labeled proteins.

RESULTS

We report here that KDM2B regulates EZH2 and BMI1 in HCT116 colon tumor cells. Knockdown of this epigenetic factor induced potent up-regulation of the protein levels of the epithelial markers E-cadherin and ZO-1, while the mesenchymal marker N-cadherin was downregulated. On the other hand, KDM2B overexpression downregulated the levels of both epithelial markers and upregulated the mesenchymal marker, suggesting control of EMT by KDM2B. In addition, RhoA, RhoB and RhoC protein levels diminished upon KDM2B-knockdown, while all three small GTPases became upregulated in KDM2B-overexpressing HCT116 cell clones. Interestingly, Rac1 GTPase level increased upon KDM2B-knockdown and diminished in KDM2B-overexpressing HCT116 colon tumor- and DU-145 prostate cancer cells.

CONCLUSIONS

These results establish a clear functional role of the epigenetic factor KDM2B in the regulation of EMT and small-GTPases expression in colon tumor cells and further support the recently postulated oncogenic role of this histone demethylase in various tumors.

摘要

背景/目的:表观遗传因子KDM2B是一种在多种肿瘤中表达的组蛋白去甲基化酶。最近,我们发现KDM2B可调节肌动蛋白细胞骨架组织、小Rho GTP酶信号传导、细胞间粘附以及前列腺肿瘤细胞的迁移。在本研究中,我们探讨了其在调节结肠肿瘤细胞上皮-间质转化(EMT)和小GTP酶表达中的作用。

方法

我们使用逆转录聚合酶链反应(RT-PCR)进行各种基因的转录分析,蛋白质印迹法评估蛋白质表达,免疫荧光显微镜观察荧光标记蛋白。

结果

我们在此报告,KDM2B在HCT116结肠肿瘤细胞中调节EZH2和BMI1。敲低这种表观遗传因子可诱导上皮标志物E-钙粘蛋白和ZO-1蛋白水平的强力上调,而间质标志物N-钙粘蛋白则下调。另一方面,KDM2B的过表达下调了两种上皮标志物的水平并上调了间质标志物,表明KDM2B可控制EMT。此外,KDM2B敲低后RhoA、RhoB和RhoC蛋白水平降低,而在过表达KDM2B的HCT116细胞克隆中,所有三种小GTP酶均上调。有趣的是,KDM2B敲低后Rac1 GTP酶水平升高,而过表达KDM2B的HCT116结肠肿瘤细胞和DU-145前列腺癌细胞中Rac1 GTP酶水平降低。

结论

这些结果明确了表观遗传因子KDM2B在调节结肠肿瘤细胞EMT和小GTP酶表达中的功能作用,并进一步支持了这种组蛋白去甲基化酶最近在各种肿瘤中假定的致癌作用。

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