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PPAR gamma suppresses the proliferation of cardiac myxoma cells through downregulation of MEF2D in a miR-122-dependent manner

机译:PPARγ抑制了MIR-122依赖的方式的MEF2D的下调了心肌肌瘤细胞的激增

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摘要

Peroxisome proliferator-activated receptor gamma (PPAR gamma), a multiple functional transcription factor, has been reported to have anti-tumor effects through inhibition of cells proliferation. However, its effects on cardiac myxoma (CM) cells and the underlying signaling mechanism is unclear. In the present study, we demonstrated that the level of PPAR gamma is inversely correlated with that of myocyte enhancer factor 2D (MEF2D), a biomarker of CM. We found that activation of PPAR gamma inhibit MEF2D expression via upregulation of miR-122, which can target the 3'-UTR of MEF2D and inhibit MEF2D expression, by directly binding to the PPRE in the miR-122 promoter region. Functional experiments further showed that miR-122-dependent downregulation of MEF2D by PPAR gamma suppress the proliferation of CM cells. These results suggest that PPAR gamma may exert its antiproliferative effects by negatively regulating the MEF2D in CM cells, which through upregulation of miR-122, and PPAR gamma/miR-122/MEF2D signaling pathway may be a novel target for treatment of CM. (C) 2016 Elsevier Inc. All rights reserved.
机译:已经据报道,过氧化物增殖剂活化受体γ(PPARγ),多功能转录因子,通过抑制细胞增殖具有抗肿瘤作用。然而,它对心肌肌瘤(CM)细胞和潜在的信号传导机制的影响尚不清楚。在本研究中,我们证明了PPARγ的水平与肌细胞增强子因子2D(MEF2D),CM的生物标志物与肌细胞增强剂因子2D(MEF2D)的水平与逆转。我们发现PPARγ的激活通过MiR-122的上调,通过UPR-122的上调来抑制MEF2D表达,其可以通过直接结合MIR-122启动子区的PPRE靶向MEF2D的3'-UTR并抑制MEF2D表达。功能实验进一步表明,PPARγ的MEF2D的miR-122依赖性下调抑制了Cm细胞的增殖。这些结果表明,PPARγ可以通过在CM细胞中对MEF2D负调节MEF2D来发挥其抗增殖作用,这通过MIR-122的上调,并且PPARγ/ miR-122 / MEF2D信号通路可以是用于治疗CM的新靶标。 (c)2016年Elsevier Inc.保留所有权利。

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