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PI3K/AKT 信号通路:miRNA 与结直肠癌中基因表达失调的关联。

The PI3K/AKT signaling pathway: Associations of miRNAs with dysregulated gene expression in colorectal cancer.

机构信息

Department of Medicine, University of Utah, Colorow, Salt Lake City, Utah.

Division of Research, Kaiser Permanente Northern California, Oakland, California.

出版信息

Mol Carcinog. 2018 Feb;57(2):243-261. doi: 10.1002/mc.22752. Epub 2017 Nov 19.

Abstract

The PI3K/AKT-signaling pathway is one of the most frequently activated signal-transduction pathways in cancer. We examined how dysregulated gene expression is associated with miRNA expression in this pathway in colorectal cancer (CRC). We used data from 217 CRC cases to evaluate differential pathway gene expression between paired carcinoma and normal mucosa and identify miRNAs that are associated with these genes. Gene expression data from RNA-Seq and miRNA expression data from Agilent Human miRNA Microarray V19.0 were analyzed. We focused on genes most associated with CRC (fold change (FC) of >1.5 or <0.67) that were statistically significant after adjustment for multiple comparisons. Of the 304 genes evaluated, 76 had a FC of <0.67, and 57 had a FC of >1.50; 47 of these genes were associated with miRNA differential expression. There were 145 mRNA:miRNA seed-region matches of which 26 were inversely associated suggesting a greater likelihood of a direct association. Most miRNA:mRNA associations were with factors that stimulated the pathway. For instance, both IL6R and PDGFRA had inverse seed-region matches with seven miRNAs, suggesting that these miRNAs have a direct effect on these genes and may be key elements in activation of the pathway. Other miRNA:mRNA associations with similar impact on the pathway were miR-203a with ITGA4, miR-6071 with ITGAV, and miR-375 with THBS2, all genes involved in extracellular matrix function that activate PI3Ks. Gene expression in the PI3K/Akt-signaling pathway is dysregulated in CRC. MiRNAs were associated with many of these dysregulated genes either directly or in an indirect manner.

摘要

PI3K/AKT 信号通路是癌症中最常被激活的信号转导通路之一。我们研究了在结直肠癌 (CRC) 中,失调的基因表达与该通路中 miRNA 表达之间的关系。我们使用了 217 例 CRC 病例的数据,评估了配对的癌组织和正常黏膜之间的通路基因表达差异,并确定了与这些基因相关的 miRNAs。分析了 RNA-Seq 的基因表达数据和 Agilent Human miRNA Microarray V19.0 的 miRNA 表达数据。我们主要关注与 CRC 最相关的基因(经多重比较调整后,倍数变化 (FC) >1.5 或 <0.67)。在所评估的 304 个基因中,有 76 个基因的 FC <0.67,57 个基因的 FC >1.50;其中 47 个基因与 miRNA 的差异表达相关。有 145 个 mRNA:miRNA 种子区匹配,其中 26 个呈负相关,这表明它们之间存在更大的直接关联可能性。大多数 miRNA:mRNA 关联与刺激通路的因素有关。例如,IL6R 和 PDGFRA 都与七个 miRNA 存在反向种子区匹配,这表明这些 miRNA 对这些基因有直接影响,并且可能是激活通路的关键因素。对通路有类似影响的其他 miRNA:mRNA 关联包括 miR-203a 与 ITGA4、miR-6071 与 ITGAV 和 miR-375 与 THBS2,它们都是参与细胞外基质功能的基因,可激活 PI3Ks。PI3K/Akt 信号通路在 CRC 中失调。许多失调基因与 miRNA 直接或间接相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b01e/5813185/3788a4658d2c/MC-57-243-g001.jpg

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