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具核梭杆菌感染的人结直肠癌细胞中 microRNA-4474/4717 表达和 CREB 结合蛋白的改变。

Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum.

机构信息

Institute of Modern Biopharmaceuticals, State Key Laboratory Breeding Base of Eco-Environment and Bio-Resource of the Three Gorges Area, Key Laboratory of Eco-environments in Three Gorges Reservoir Region, Ministry of Education, School of Life Sciences, Southwest University, Chongqing, China.

Department of Clinical Microbiology and Immunology, Southwest Hospital & College of Pharmacy and Medical Laboratory Science, Army Medical University (Third Military Medical University), Chongqing, China.

出版信息

PLoS One. 2019 Apr 5;14(4):e0215088. doi: 10.1371/journal.pone.0215088. eCollection 2019.

Abstract

Colorectal cancer (CRC) is a common and highly lethal form of cancer. Although the etiologic role of Fusobacterium nucleatum (F. nucleatum) in the development of CRC has been elucidated, the specific tumor molecules involved in the progression of CRC induced by F. nucleatum have not been identified. This study investigated several miRNAs and genes involved in the progression of F. nucleatum-induced CRC by Affymetrix miRNA microarray technology and GeneChip Human Transcriptome Array 2.0. The results suggest that miR-4474 and miR-4717 are up-regulated in CRC tissues in response to F. nucleatum infection, compared with the control group (paracancerous tissues), while other genes associated with signaling pathways in cancer, including CREB-binding protein (CREBBP), STAT1, PRKACB, CAMK2B, JUN, TP53 and EWSR1, were dysregulated. Bioinformatic analysis identified CREBBP as the primary aberrantly expressed gene in F. nucleatum-induced CRC. Consistent with the microarray analysis results, real-time RT-PCR analysis demonstrated that the expression of miR-4474/4717 was upregulated while that of CREBBP mRNA was downregulated in CRC patients infected with F. nucleatum. Additionally, CREBBP was identified as a novel target of miR-4474/4717. The results of this study suggest that miR-4474 and miR-4717 are involved in the progression of F. nucleatum-induced CRC by posttranscriptionally regulating the target gene CREBBP.

摘要

结直肠癌(CRC)是一种常见且致命性很高的癌症。虽然具核梭杆菌(F. nucleatum)在 CRC 的发展中的病因学作用已经阐明,但涉及 F. nucleatum 诱导的 CRC 进展的特定肿瘤分子尚未确定。本研究通过 Affymetrix miRNA 微阵列技术和 GeneChip Human Transcriptome Array 2.0 研究了与 F. nucleatum 诱导的 CRC 进展相关的几种 miRNA 和基因。结果表明,与对照组(癌旁组织)相比,CRC 组织中 miR-4474 和 miR-4717 对 F. nucleatum 感染的反应呈上调,而其他与癌症信号通路相关的基因,包括 CREB 结合蛋白(CREBBP)、STAT1、PRKACB、CAMK2B、JUN、TP53 和 EWSR1,均失调。生物信息学分析确定 CREBBP 是 F. nucleatum 诱导的 CRC 中主要异常表达的基因。与微阵列分析结果一致,实时 RT-PCR 分析表明,感染 F. nucleatum 的 CRC 患者中 miR-4474/4717 的表达上调,而 CREBBP mRNA 的表达下调。此外,还鉴定出 CREBBP 是 miR-4474/4717 的新靶基因。本研究结果表明,miR-4474 和 miR-4717 通过转录后调节靶基因 CREBBP 参与 F. nucleatum 诱导的 CRC 进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83f2/6450631/b5fb701d0bbf/pone.0215088.g001.jpg

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