Analysis Network Centrality Reveals SignificantGenes in Breast Cancer

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This study used SNP information and gene network analysis to identify key breast cancer–related genes by applying three community detection algorithms (Spinglass, Girvan-Newman, and Belief) and selecting the best approach via principal component analysis. The authors then computed four centrality measures (betweenness, degree, closeness, and maximal clique centrality) to rank the most significant genes, resulting in 42 genes overall, including ESR1, BRD4, FRYL, MYO5A, NTN1, PPFIBP1, and STAT3, with ESR1 highlighted as linked to breast cancer. The paper reports validation that ESR1, BRD4, FRYL, and STAT3 are associated with breast cancer, but it is a preprint and not peer reviewed. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Analysis Network Centrality Reveals SignificantGenes in Breast Cancer | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article Analysis Network Centrality Reveals SignificantGenes in Breast Cancer Angga Aditya Permana, Wisnu Ananta Kusuma, Sri Nurdiati, Irmanida Batubara This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-6467306/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Breast cancer is a complex disease that requires early detection for effective treat-ment. Single nucleotide polymorphism (SNPs) help identify associations betweengenetic variation and cancer susceptibility. Network analysis facilities SNP selec-tion and maps their location within specific genes. This study aimed to identifykey breast cancer-related genes using three community detection algorithms:Spinglass, Girvan-Newman and Belief. The best algorithm was determined usingprincipal component analysis (PCA), while the most significant genes were iden-tified based on four centrality measures: betwenness, degree, closeness, maximal1clique centrality. The analysis identified 42 specific genes, with seven genes(ESR1, BRD4, FRYL, MYO5A, NTN1, PPFIBP1 and STAT3) listed in theCatalogue of Somatic Mutations in Cancer (COSMIC). Additionally, five genes(ESR1, BRD4, FRYL, PPFIBP1 and STAT3) were recognized as the hallmarksof cancer, with ESR1 specifically linked to breast cancer. Validation confirmedthat ESR1, BRD4, FRYL and STAT3 are associated with breast cancer. Thefindings highlight the potential of network centrality in identifying key genesrelated to breast cancer. breast cancer community detection gene network analysis SNP Full Text Additional Declarations No competing interests reported. Cite Share Download PDF Status: Posted Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. Our growing team is made up of researchers and industry professionals working together to solve the most critical problems facing scientific publishing. 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