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Genomic Loss Of Microrna-101 Leads To Overexpression Of Histone Methyltransferase Ezh2 In Cancer

机译:Microrna-101基因组丢失导致组蛋白甲基转移酶Ezh2在癌症中的过度表达

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Enhancer of zeste homolog 2 (EZH2) is a mammalian histone methyltransferase that contributes to the epigenetic silencing of target genes and regulates the survival and metastasis of cancer cells. EZH2 is overexpressed in aggressive solid tumors by mechanisms that remain unclear. Here we show that the expression and function of EZH2 in cancer cell lines are inhibited by microRNA-101 (miR-101). Analysis of human prostate tumors revealed that miR-101 expression decreases during cancer progression, paralleling an increase in EZH2 expression. One or both of the two genomic loci encoding miR-101 were somatically lost in 37.5% of clinically localized prostate cancer cells (6 of 16) and 66.7% of metastatic disease cells (22 of 33). We propose that the genomic loss of miR-101 in cancer leads to overexpression of EZH2 and concomitant dysregulation of epigenetic pathways, resulting in cancer progression.
机译:zeste同源物2(EZH2)的增强子是一种哺乳动物组蛋白甲基转移酶,可促进靶基因的表观遗传沉默,并调节癌细胞的存活和转移。通过尚不清楚的机制,EZH2在侵袭性实体瘤中过表达。在这里,我们显示EZH2在癌细胞系中的表达和功能受到microRNA-101(miR-101)的抑制。对人前列腺肿瘤的分析显示,miR-101表达在癌症进展过程中降低,与EZH2表达增加平行。编码miR-101的两个基因组基因座中的一个或两个在体格失调的临床定位的前列腺癌细胞中占37.5%(16个中的6个),而在转移性疾病细胞中则占66.7%(33个中的22个)。我们提出癌症中miR-101的基因组丢失会导致EZH2的过表达和表观遗传途径的异常调节,从而导致癌症进展。

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