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长链非编码 RNA NEAT1 参与癌症发生。

Involvement of the long noncoding RNA NEAT1 in carcinogenesis.

机构信息

Division of Oncology, Department of Internal Medicine, Medical University of Graz (MUG), Austria.

Research Unit for Non-coding RNAs and Genome Editing, Medical University of Graz (MUG), Austria.

出版信息

Mol Oncol. 2019 Jan;13(1):46-60. doi: 10.1002/1878-0261.12404. Epub 2018 Dec 3.

Abstract

Altered expression levels of the long noncoding RNA (lncRNA) nuclear-enriched abundant transcript 1 (NEAT1) have been reported in different types of cancer. More than half of the NEAT1 studies in cancer have been published within the last 2 years. In this review, we discuss very recent developments and insights into NEAT1 contribution to carcinogenesis. Summarizing the literature, it becomes obvious that NEAT1 is a lncRNA highly de-/upregulated in a variety of cancer entities, in which it primarily acts as a competing endogenous RNA (ceRNA) which sponges tumor-suppressive microRNA (miRNA). The sponged miRNA lose their ability to degrade, silence, or hamper translation of their downstream-mostly oncogenic-target transcripts, ultimately promoting carcinogenesis. This role of NEAT1 function in tumorigenesis suggests it may be a prognostic biomarker as well as potential therapeutic target, pending the completion of further studies into the underlying mechanisms.

摘要

长链非编码 RNA(lncRNA)核丰富转录本 1(NEAT1)的表达水平改变已在不同类型的癌症中报道。在癌症中,超过一半的 NEAT1 研究是在过去 2 年内发表的。在这篇综述中,我们讨论了 NEAT1 对致癌作用的最新发展和见解。总结文献,很明显 NEAT1 是一种在多种癌症实体中高度下调/上调的 lncRNA,主要作为竞争性内源 RNA(ceRNA),可吸收肿瘤抑制性 microRNA(miRNA)。被吸收的 miRNA 失去了降解、沉默或阻碍其下游致癌靶转录物翻译的能力,最终促进了癌症的发生。NEAT1 在肿瘤发生中的这种功能作用表明,它可能是一个预后生物标志物,也是一个潜在的治疗靶点,但需要进一步研究其潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9463/6322192/956fed0d1e0f/MOL2-13-46-g001.jpg

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