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一种综合方法,利用新参数绘制差异表达基因和网络组件,以阐明结直肠癌中的关键调控基因。

An Integrative Approach for Mapping Differentially Expressed Genes and Network Components Using Novel Parameters to Elucidate Key Regulatory Genes in Colorectal Cancer.

作者信息

Sehgal Manika, Gupta Rajinder, Moussa Ahmed, Singh Tiratha Raj

机构信息

Department of Biotechnology and Bioinformatics, Jaypee University of Information Technology (JUIT), Waknaghat, Solan, H.P. 173234, India.

LabTIC Laboratory, ENSA, Abdelmalek Essaadi University, Tangier, Morocco.

出版信息

PLoS One. 2015 Jul 29;10(7):e0133901. doi: 10.1371/journal.pone.0133901. eCollection 2015.

Abstract

For examining the intricate biological processes concerned with colorectal cancer (CRC), a systems biology approach integrating several biological components and other influencing factors is essential to understand. We performed a comprehensive system level analysis for CRC which assisted in unravelling crucial network components and many regulatory elements through a coordinated view. Using this integrative approach, the perceptive of complexity hidden in a biological phenomenon is extensively simplified. The microarray analyses facilitated differential expression of 631 significant genes employed in the progression of disease and supplied interesting associated up and down regulated genes like jun, fos and mapk1. The transcriptional regulation of these genes was deliberated widely by examining transcription factors such as hnf4, nr2f1, znf219 and dr1 which directly influence the expression. Further, interactions of these genes/proteins were evaluated and crucial network motifs were detected to associate with the pathophysiology of CRC. The available standard statistical parameters such as z-score, p-value and significance profile were explored for the identification of key signatures from CRC pathway whereas a few novel parameters representing over-represented structures were also designed in the study. The applied approach revealed 5 key genes i.e. kras, araf, pik3r5, ralgds and akt3 via our novel designed parameters illustrating high statistical significance. These novel parameters can assist in scrutinizing candidate markers for diseases having known biological pathways. Further, investigating and targeting these proposed genes for experimental validations, instead being spellbound by the complicated pathway will certainly endow valuable insight in a well-timed systematic understanding of CRC.

摘要

为了研究与结直肠癌(CRC)相关的复杂生物学过程,整合多种生物成分和其他影响因素的系统生物学方法对于理解这一过程至关重要。我们对CRC进行了全面的系统水平分析,通过协调的视角协助揭示关键的网络成分和许多调控元件。使用这种综合方法,生物现象中隐藏的复杂性认知得到了广泛简化。微阵列分析促进了631个在疾病进展中起重要作用的基因的差异表达,并提供了如jun、fos和mapk1等有趣的相关上调和下调基因。通过研究直接影响表达的转录因子如hnf4、nr2f1、znf219和dr1,对这些基因的转录调控进行了广泛探讨。此外,评估了这些基因/蛋白质的相互作用,并检测到关键的网络基序与CRC的病理生理学相关。研究探索了可用的标准统计参数如z分数、p值和显著性概况,以从CRC途径中识别关键特征,同时还设计了一些代表过度表达结构的新参数。应用的方法通过我们新设计的参数揭示了5个关键基因,即kras、araf、pik3r5、ralgds和akt3,具有很高的统计学意义。这些新参数有助于审查具有已知生物学途径的疾病的候选标志物。此外,研究并针对这些提出的基因进行实验验证,而不是被复杂的途径所迷惑,肯定会为及时系统地理解CRC提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84dc/4519280/2baa8e25c2ba/pone.0133901.g001.jpg

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