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CRTC1-MAML2 融合诱导长非编码 RNA LINC00473 的表达维持人黏液表皮样癌细胞的生长和存活。

CRTC1-MAML2 fusion-induced lncRNA LINC00473 expression maintains the growth and survival of human mucoepidermoid carcinoma cells.

机构信息

Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL, USA.

UF Health Cancer Center, University of Florida, Gainesville, FL, USA.

出版信息

Oncogene. 2018 Apr;37(14):1885-1895. doi: 10.1038/s41388-017-0104-0. Epub 2018 Jan 22.

Abstract

Mucoepidermoid carcinoma (MEC) arises in many glandular tissues and contributes to the most common malignant salivary gland cancers. MEC is specifically associated with a unique t(11;19) translocation and the resulting CRTC1-MAML2 fusion is a major oncogenic driver for MEC initiation and maintenance. However, the molecular basis underlying the CRTC1-MAML2 oncogenic functions remains elusive. Through gene expression profiling analysis, we observed that LINC00473, a long non-coding RNA (lncRNA), was the top down-regulated target in CRTC1-MAML2-depleted human MEC cells. LncRNAs belong to a new class of non-coding RNAs with emerging roles in tumorigenesis and progression, but remain poorly characterized. In this study, we investigated the role of LINC00473 in mediating CRTC1-MAML2 oncogenic activity in human MEC. We found that LINC00473 transcription was significantly induced in human CRTC1-MAML2-positive MEC cell lines and primary MEC tumors, and was tightly correlated with the CRTC1-MAML2 RNA level. LINC00473 induction was dependent on the ability of CRTC1-MAML2 to activate CREB-mediated transcription. Depletion of LINC00473 significantly reduced the proliferation and survival of human MEC cells in vitro and blocked the in vivo tumor growth in a human MEC xenograft model. RNA in situ hybridization analysis demonstrated a predominantly nuclear localization pattern for LINC00473 in human MEC cells. Furthermore, gene expression profiling revealed that LINC00473 depletion resulted in differential expression of genes important in cancer cell growth and survival. LINC00473 likely regulates gene expression in part through its ability to bind to a cAMP signaling pathway component NONO, enhancing the ability of CRTC1-MAML2 to activate CREB-mediated transcription. Our overall results demonstrate that LINC00473 is a downstream target and an important mediator of the CRTC1-MAML2 oncoprotein. Therefore, LINC00473 acts as a promising biomarker and therapeutic target for human CRTC1-MAML2-positive MECs.

摘要

黏液表皮样癌 (MEC) 发生于多种腺体组织,是最常见的恶性涎腺肿瘤。MEC 特别与独特的 t(11;19)易位相关,由此产生的 CRTC1-MAML2 融合是 MEC 起始和维持的主要致癌驱动因素。然而,CRTC1-MAML2 致癌功能的分子基础仍不清楚。通过基因表达谱分析,我们观察到长链非编码 RNA (lncRNA) LINC00473 是 CRTC1-MAML2 耗尽的人 MEC 细胞中下调最明显的靶标。lncRNA 属于一类新的非编码 RNA,在肿瘤发生和进展中具有新兴作用,但特征描述较差。在这项研究中,我们研究了 LINC00473 在介导人 MEC 中 CRTC1-MAML2 致癌活性中的作用。我们发现 LINC00473 在人 CRTC1-MAML2 阳性 MEC 细胞系和原发性 MEC 肿瘤中显著诱导,与 CRTC1-MAML2 RNA 水平紧密相关。LINC00473 的诱导依赖于 CRTC1-MAML2 激活 CREB 介导的转录的能力。LINC00473 的耗竭显著降低了人 MEC 细胞在体外的增殖和存活,并在人 MEC 异种移植模型中阻断了体内肿瘤生长。RNA 原位杂交分析表明 LINC00473 在人 MEC 细胞中主要定位于核内。此外,基因表达谱分析显示 LINC00473 的耗竭导致与癌细胞生长和存活相关的重要基因的差异表达。LINC00473 可能通过其与 cAMP 信号通路成分 NONO 结合的能力部分调节基因表达,增强 CRTC1-MAML2 激活 CREB 介导的转录的能力。我们的总体结果表明,LINC00473 是 CRTC1-MAML2 癌蛋白的下游靶标和重要介质。因此,LINC00473 是人类 CRTC1-MAML2 阳性 MEC 的有前途的生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df26/5889358/de855145daee/nihms925044f1.jpg

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