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MDM4 regulation by the let-7 miRNA family in the DNA damage response of glioma cells.

FEBS letters (2015-06-02)
Chen Xie, Wei Chen, Mengdie Zhang, Qiuxian Cai, Weiyi Xu, Xiaodi Li, Songshan Jiang
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Despite extensive investigation into the role of let-7 miRNAs in pathological tumor processes, their involvement in the DNA damage response remains unclear. Here we show that most let-7 family members down-regulate MDM4 expression via binding to MDM4 mRNA at a conserved DNA sequence. Expression of exogenous let-7 miRNA mimics decreased MDM4 protein but not mRNA levels. Several DNA damage reagents increased let-7 expression, thereby decreasing MDM4 protein levels in glioma cells. Inhibition of endogenous let-7 with antisense RNAs rescued MDM4 protein levels with or without MG132, a proteasome-dependent degradation inhibitor. An MDM4 mutation identified in a glioma patient was associated with loss of the putative MDM4 target site. Therefore, let-7 binding to MDM4 is implicated in the DNA damage response.

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cis-Diamminplatin(II)-dichlorid, crystalline
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Hydroxyharnstoff, 98%, powder
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cis-Diaminplatin(II)-dichlorid, ≥99.9% trace metals basis
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trans-Platin(II)diammindichlorid