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Drug compound prediction-based analysis of cigarette smoking to Pancreatic Cancer patients: A Bioinformatics study

机译:胰腺癌患者吸烟的药物复合预测分析:生物信息学研究

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Considering the fact of survival rate, pancreatic cancer (PC) can be categorized among the most fatal cancer diseases as the survival rate is medium among most of the cases. Cigarette smoking is regarded as a significant risk factor for PC. In this study, therapeutic results are attempted to be found by the assist of a number of Bioinformatics tools. Two microarray datasets GSE144909 and GSE26307 are used for pancreatic cancer and active smoker lung cell samples respectively. Preprocessing and filtering of the datasets and common differentially expressed genes (DEGs) are identified with the assist of R programming language. Regulation of the DEGs are expressed with a Venn diagram. Then Protein-protein interactions (PPIs) network is designed based on the common DEGs and hub nodes are identified using topological analysis. RPA1, RPA2, BLM, FANCM and APITD1 genes are the top 5 mostly interconnected genes in PPIs network and visibility of RPA1 and RPA2 is found in inflammatory pancreatic cancer cell and smoker lung cell. Gene ontology (GO) and pathway identification is regarded as the future study of this research. Finally, a number of therapeutic targets have been identified based on the common DEGs.
机译:考虑到生存率的事实,胰腺癌(PC)可以在大多数病例中存活率中致死最致命的癌症疾病中分类。吸烟被认为是PC的重要风险因素。在这项研究中,试图通过许多生物信息工具的辅助来发现治疗结果。两个微阵列数据集GSE144909和GSE26307分别用于胰腺癌和活性吸烟者肺细胞样本。利用R编程语言的辅助来识别数据集和常用差异表达基因(DEGS)的预处理和滤波。对DEG的调节用VENN图表表达。然后基于常见的DEGS和集线器节点设计蛋白质 - 蛋白质相互作用(PPI)网络,使用拓扑分析识别。 RPA1,RPA2,BLM,FANCM和APITD1基因是PPI网络中的前5个主要互连基因,RPA1和RPA2的可见度在炎性胰腺癌细胞和吸烟者肺细胞中发现。基因本体(GO)和途径识别被认为是该研究的未来研究。最后,已经基于常见的参数鉴定了许多治疗靶标。

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