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Main Authors: Bhattacharjya, Abanti, Islam, Md Manowarul, Uddin, Md Ashraf, Talukder, Md. Alamin, Azad, AKM, Aryal, Sunil, Paul, Bikash Kumar, Tasnim, Wahia, Almoyad, Muhammad Ali Abdulllah, Moni, Mohammad Ali
Format: Preprint
Published: 2024
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Online Access:https://arxiv.org/abs/2402.17807
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author Bhattacharjya, Abanti
Islam, Md Manowarul
Uddin, Md Ashraf
Talukder, Md. Alamin
Azad, AKM
Aryal, Sunil
Paul, Bikash Kumar
Tasnim, Wahia
Almoyad, Muhammad Ali Abdulllah
Moni, Mohammad Ali
author_facet Bhattacharjya, Abanti
Islam, Md Manowarul
Uddin, Md Ashraf
Talukder, Md. Alamin
Azad, AKM
Aryal, Sunil
Paul, Bikash Kumar
Tasnim, Wahia
Almoyad, Muhammad Ali Abdulllah
Moni, Mohammad Ali
contents With the advent of Information technology, the Bioinformatics research field is becoming increasingly attractive to researchers and academicians. The recent development of various Bioinformatics toolkits has facilitated the rapid processing and analysis of vast quantities of biological data for human perception. Most studies focus on locating two connected diseases and making some observations to construct diverse gene regulatory interaction networks, a forerunner to general drug design for curing illness. For instance, Hypopharyngeal cancer is a disease that is associated with EGFR-mutated lung adenocarcinoma. In this study, we select EGFR-mutated lung adenocarcinoma and Hypopharyngeal cancer by finding the Lung metastases in hypopharyngeal cancer. To conduct this study, we collect Mircorarray datasets from GEO (Gene Expression Omnibus), an online database controlled by NCBI. Differentially expressed genes, common genes, and hub genes between the selected two diseases are detected for the succeeding move. Our research findings have suggested common therapeutic molecules for the selected diseases based on 10 hub genes with the highest interactions according to the degree topology method and the maximum clique centrality (MCC). Our suggested therapeutic molecules will be fruitful for patients with those two diseases simultaneously.
format Preprint
id arxiv_https___arxiv_org_abs_2402_17807
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Exploring Gene Regulatory Interaction Networks and predicting therapeutic molecules for Hypopharyngeal Cancer and EGFR-mutated lung adenocarcinoma
Bhattacharjya, Abanti
Islam, Md Manowarul
Uddin, Md Ashraf
Talukder, Md. Alamin
Azad, AKM
Aryal, Sunil
Paul, Bikash Kumar
Tasnim, Wahia
Almoyad, Muhammad Ali Abdulllah
Moni, Mohammad Ali
Genomics
Machine Learning
With the advent of Information technology, the Bioinformatics research field is becoming increasingly attractive to researchers and academicians. The recent development of various Bioinformatics toolkits has facilitated the rapid processing and analysis of vast quantities of biological data for human perception. Most studies focus on locating two connected diseases and making some observations to construct diverse gene regulatory interaction networks, a forerunner to general drug design for curing illness. For instance, Hypopharyngeal cancer is a disease that is associated with EGFR-mutated lung adenocarcinoma. In this study, we select EGFR-mutated lung adenocarcinoma and Hypopharyngeal cancer by finding the Lung metastases in hypopharyngeal cancer. To conduct this study, we collect Mircorarray datasets from GEO (Gene Expression Omnibus), an online database controlled by NCBI. Differentially expressed genes, common genes, and hub genes between the selected two diseases are detected for the succeeding move. Our research findings have suggested common therapeutic molecules for the selected diseases based on 10 hub genes with the highest interactions according to the degree topology method and the maximum clique centrality (MCC). Our suggested therapeutic molecules will be fruitful for patients with those two diseases simultaneously.
title Exploring Gene Regulatory Interaction Networks and predicting therapeutic molecules for Hypopharyngeal Cancer and EGFR-mutated lung adenocarcinoma
topic Genomics
Machine Learning
url https://arxiv.org/abs/2402.17807