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MicroRNA‐transcription factor interactions and their combined effect on target gene expression in colon cancer cases

机译:微血管转录因子相互作用及其对结肠癌病例靶基因表达的综合影响

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Abstract Transcription factors (TFs) and microRNAs (miRNAs) regulate gene expression: TFs by influencing messenger RNA (mRNA) transcription and miRNAs by influencing mRNA translation and transcript degradation. Additionally, miRNAs and TFs alter each other's expression, making it difficult to ascertain the effect either one has on target gene (TG) expression. In this investigation, we use a two‐way interaction model with the TF and miRNA as independent variables to investigate whether miRNAs and TFs work together to influence TG expression levels in colon cancer subjects. We used known TF binding sites and validated miRNA targets to determine potential miRNA‐TF‐TG interactions, restricting interactions to those with a TF previously associated with altered risk of colorectal cancer death. We analyzed interactions using normal colonic mucosa expression as well as differential expression, which is measured as colonic carcinoma expression minus normal colonic mucosa expression. We analyzed 3518 miRNA‐TF‐TG triplets using normal mucosa expression and 617 triplets using differential expression. Normal colonic RNA‐Seq data were available for 168 individuals; of these, 159 also had carcinoma RNA‐Seq data. Thirteen unique miRNA‐TF‐TG interactions, comprising six miRNAs, four TFs, and 11 TGs, were statistically significant after adjustment for multiple comparisons in normal colonic mucosa, and 14 unique miRNA‐TF‐TG interactions, comprising two miRNAs, two TFs, and 13 TGs, were found for carcinoma‐normal differential expression. Our results show that TG expression is influenced by both miRNAs as well as TFs, and the influence of one regulator impacts the effect of the other on the shared TG expression.
机译:摘要转录因子(TFS)和MicroRNA(miRNA)通过影响MRNA翻译和转录物降解来调节基因表达:TFS通过影响MRNA平移和转录性降解。此外,miRNA和TFS改变彼此的表达,使得难以确定一个对靶基因(TG)表达的影响。在该研究中,我们使用双向相互作用模型与TF和miRNA作为独立变量,以研究MiRNA和TFS是否共同努力,影响结肠癌受试者的TG表达水平。我们使用已知的TF结合位点和验证的miRNA靶标以确定潜在的miRNA-TF-Tg相互作用,限制与先前与结直肠癌死亡风险改变相关的TF的相互作用。我们分析了使用正常结肠粘膜表达的相互作用以及差异表达,其被测量为结肠癌表达减去正常正常结肠粘膜表达。使用常规粘膜表达和使用差异表达分析3518 miRNA-TF-TG三联体和617个三胞胎。适用于168人的正常结肠RNA-SEQ数据;其中,159也有癌RNA-SEQ数据。包含六个miRNA,四种TF和11 TGS的十三个独特的miRNA-TF-TG相互作用在正常结肠粘膜中的多重比较后进行统计学意义,并且14个独特的miRNA-TF相互作用,包括两个miRNA,两个TFS,发现了13吨,用于癌正常差异表达。我们的结果表明,TG表达受MiRNA和TFS的影响,一个调节器的影响会影响另一个对共同的TG表达的影响。

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