骨质疏松症基因相互作用组的分析鉴定异质基因及其途径

Bharat Singh, Yasha Hasija
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引用次数: 1

摘要

遗传学的最新进展促使人们在有效识别复杂疾病中纠缠在一起的基因方面取得了迅速进展。尽管如此,全面理解基因的生理和分子机制之间的关系以及它们如何影响疾病表型仍然是研究人员和临床医生面临的挑战。在这里,我们希望确定骨质疏松症疾病模块,即相互作用组的本地邻域,其躁动与骨质疏松症有关,并使用计算和实验方法为功能和病理生理应用提供支持。近年来对骨质疏松症的研究表明,对于某些遗传变异,患病和正常情况下的基因表达水平是不同的。骨质疏松症疾病模块补充了不确定的GWAS p值,也可能包含与其他疾病模块共同的机制。因此,我们构建了104个基因的基因-基因和蛋白-蛋白相互作用网络,其中173个snp已报道,并进行了GO功能富集和KEGG通路富集分析,识别了骨质疏松的实质性基因及其分子功能。我们的分析表明,SOST和LRP5的多态性是非常保守的snp。•Benchside:对骨质疏松症的原始数据进行稳健和简明的管理,将有助于使症状前数据更有价值,以进行湿实验室研究。•床边:生物信息学网络研究对于寻找药物靶点至关重要,因此有必要对骨质疏松症的大量数据进行处理,以策划和产生有意义的靶点。此外,可以探索不可预测的途径和基因,以支持临床研究。•行业:来自疾病网络研究的数据对于预测临床和非临床随访以更好地开发药物至关重要。•社区:批准和标准化多余的骨质疏松症和基因多态性数据有助于即兴药物靶点的临床验证。重要的是,数据达到适当的严格级别。•政府:就药物开发的最终目的而言,精炼的基因表达数据是开发临床产品的关键。政府为生产和验证此类产品提供的财政支持非常重要,因为随着时间的推移,这些支持将对患者和临床医生都有帮助。
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Analysis of osteoporosis gene interactome to identify heterogenic genes and pathways

Latest advances in genetics have prompted swift progress towards the efficient identification of genes tangled in complex diseases. Still, the comprehensive understanding of the relation between the physiological and molecular mechanism of genes and how they affect disease phenotypes remains a challenge for researchers and clinicians. Here, we wish to identify the osteoporosis disease module, i.e. the indigenous neighborhood of the interactome whose agitation is associated with osteoporosis, and endorse it for functional and pathophysiological application, using both computational and experimental methodologies. Recent studies in osteoporosis suggest that against certain genetic variations, the expression level of genes were different in both diseased and normal conditions. The osteoporosis disease module supplemented with uncertain GWAS p-values may also contain mechanisms that are collective with other disease modules. We, therefore, constructed the gene-gene and protein-protein interaction network for 104 genes with 173 reported SNPs accompanied by GO functional enrichment and KEGG pathway enrichment analysis and recognized the substantial genes of osteoporosis along with their molecular functions. Our analyses exposed polymorphism in SOST and LRP5 as significantly conservative SNPs.

Focal points

  • Benchside: Robust and concise curation of raw data for osteoporosis will help to make the presymptomatic data more valuable to perform wet lab studies.

  • Bedside: Bioinformatics network studies are crucial in finding drug targets so it becomes necessary to process the huge data for osteoporosis to curate and produce significance targets. Further, unpredicted pathways and genes could be explored to support clinical studies.

  • Industry: Data from disease network studies is essential for predicting clinical and non-clinical follow-ups for better drug development.

  • Community: Ratification and standardization of redundant osteoporosis and gene polymorphism data helps to improvise clinical validation of drug targets. It is important that the data is upto the proper stringency level.

  • Government: As for the ultimate purpose of drug development, refined gene expression data is the key in developing clinical products. Financial support from government to produce and validate such products is important as with time these will help both the patients and clinicians as well.

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Contents Editorial Board Improving disease diagnosis by a new hybrid model Pros, cons and future of antibiotics Abstracts: 5th Annual Congress of the European Society for Translational Medicine (EUSTM-2017), 20-22 October 2017, Berlin, Germany
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