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人类内源性逆转录病毒 K 和长散在核元件 1 DNA 的甲基化与再表达在膀胱癌中的研究。

HERV-K and LINE-1 DNA Methylation and Reexpression in Urothelial Carcinoma.

机构信息

Department of Urology, Medical Faculty, Heinrich Heine University , Düsseldorf , Germany.

出版信息

Front Oncol. 2013 Sep 26;3:255. doi: 10.3389/fonc.2013.00255. eCollection 2013.

Abstract

Changes in DNA methylation frequently accompany cancer development. One prominent change is an apparently genome-wide decrease in methylcytosine that is often ascribed to DNA hypomethylation at retroelements comprising nearly half the genome. DNA hypomethylation may allow reactivation of retroelements, enabling retrotransposition, and causing gene expression disturbances favoring tumor development. However, neither the extent of hypomethylation nor of retroelement reactivation are precisely known. We therefore assessed DNA methylation and expression of three major classes of retroelements (LINE-1, HERV-K, and AluY) in human urinary bladder cancer tissues and cell lines by pyrosequencing and quantitative reverse transcription-polymerase chain reaction, respectively. We found substantial global LINE-1 DNA hypomethylation in bladder cancer going along with a shift toward full-length LINE-1 expression. Thus, pronounced differences in LINE-1 expression were observed, which may be promoted, among others, by LINE-1 hypomethylation. Significant DNA hypomethylation was found at the HERV-K_22q11.23 proviral long terminal repeat (LTR) in bladder cancer tissues but without reactivation of its expression. DNA methylation of HERVK17, essentially absent from normal urothelial cells, was elevated in cell lines from invasive bladder cancers. Accordingly, the faint expression of HERVK17 in normal urothelial cells disappeared in such cancer cell lines. Of 16 additional HERV-Ks, expression of 7 could be detected in the bladder, albeit generally at low levels. Unlike in prostate cancers, none of these showed significant expression changes in bladder cancer. In contrast, expression of the AluYb8 but not of the AluYa5 family was significantly increased in bladder cancer tissues. Collectively, our findings demonstrate a remarkable specificity of changes in expression and DNA methylation of retroelements in bladder cancer with a significantly different pattern from that in prostate cancer.

摘要

DNA 甲基化的改变常伴随着癌症的发生。一个显著的变化是甲基胞嘧啶在整个基因组中明显减少,这种减少通常归因于构成基因组近一半的反转录元件的 DNA 去甲基化。DNA 去甲基化可能允许反转录元件重新激活,从而导致反转录转座,并引起有利于肿瘤发展的基因表达紊乱。然而,DNA 去甲基化的程度和反转录元件的重新激活都不是精确可知的。因此,我们通过焦磷酸测序和定量逆转录聚合酶链反应分别评估了人膀胱癌组织和细胞系中三种主要类型的反转录元件(LINE-1、HERV-K 和 AluY)的 DNA 甲基化和表达。我们发现膀胱癌中存在大量的 LINE-1 DNA 去甲基化,伴随着全长 LINE-1 表达的转移。因此,观察到明显的 LINE-1 表达差异,这些差异可能除其他因素外,还受到 LINE-1 去甲基化的促进。在膀胱癌组织中,HERV-K_22q11.23 前病毒长末端重复(LTR)的 DNA 也发现显著的去甲基化,但没有重新激活其表达。在侵袭性膀胱癌的细胞系中,基本上不存在于正常尿路上皮细胞中的 HERVK17 的 DNA 甲基化水平升高。因此,HERVK17 在正常尿路上皮细胞中的微弱表达在这些癌细胞系中消失了。在另外的 16 种 HERV-K 中,有 7 种在膀胱中可以检测到表达,尽管通常水平较低。与前列腺癌不同的是,在膀胱癌中,这些 HERV-K 没有一个表现出明显的表达变化。相反,AluYb8 的表达在膀胱癌组织中显著增加,但 AluYa5 家族的表达没有增加。总的来说,我们的研究结果表明,在膀胱癌中,反转录元件的表达和 DNA 甲基化的改变具有显著的特异性,与前列腺癌的改变模式显著不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8df4/3783855/37c7be62d5e3/fonc-03-00255-g001.jpg

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