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增强子 RNA 在癌症中作为 eRNA 靶向治疗的转录景观和临床应用。

Transcriptional landscape and clinical utility of enhancer RNAs for eRNA-targeted therapy in cancer.

机构信息

Department of Biochemistry and Molecular Biology, McGovern Medical School at The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.

Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.

出版信息

Nat Commun. 2019 Oct 8;10(1):4562. doi: 10.1038/s41467-019-12543-5.

Abstract

Enhancer RNA (eRNA) is a type of noncoding RNA transcribed from the enhancer. Although critical roles of eRNA in gene transcription control have been increasingly realized, the systemic landscape and potential function of eRNAs in cancer remains largely unexplored. Here, we report the integration of multi-omics and pharmacogenomics data across large-scale patient samples and cancer cell lines. We observe a cancer-/lineage-specificity of eRNAs, which may be largely driven by tissue-specific TFs. eRNAs are involved in multiple cancer signaling pathways through putatively regulating their target genes, including clinically actionable genes and immune checkpoints. They may also affect drug response by within-pathway or cross-pathway means. We characterize the oncogenic potential and therapeutic liability of one eRNA, NET1e, supporting the clinical feasibility of eRNA-targeted therapy. We identify a panel of clinically relevant eRNAs and developed a user-friendly data portal. Our study reveals the transcriptional landscape and clinical utility of eRNAs in cancer.

摘要

增强子 RNA(eRNA)是一种从增强子转录而来的非编码 RNA。尽管 eRNA 在基因转录调控中的关键作用已逐渐被认识,但 eRNA 在癌症中的系统景观和潜在功能在很大程度上仍未被探索。在这里,我们报告了跨大规模患者样本和癌细胞系整合多组学和药物基因组学数据。我们观察到 eRNA 的癌症/谱系特异性,这可能主要由组织特异性 TF 驱动。eRNA 通过推测调节其靶基因(包括临床上可操作的基因和免疫检查点)参与多种癌症信号通路。它们也可能通过途径内或途径间的方式影响药物反应。我们描述了一个 eRNA,NET1e 的致癌潜力和治疗负担,支持了 eRNA 靶向治疗的临床可行性。我们确定了一组临床相关的 eRNA,并开发了一个用户友好的数据门户。我们的研究揭示了 eRNA 在癌症中的转录景观和临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dde/6783481/2f0f575c0b0b/41467_2019_12543_Fig1_HTML.jpg

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