Abstract PR06: Analysis of enhancer transcription reveals novel gene regulatory networks in breast cancer

Author(s):  
Hector L. Franco ◽  
Anusha Nagari ◽  
Yuanxin Xi ◽  
Wenqian Li ◽  
Dana Richardson ◽  
...  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Luis F. Iglesias-Martinez ◽  
Barbara De Kegel ◽  
Walter Kolch

AbstractReconstructing gene regulatory networks is crucial to understand biological processes and holds potential for developing personalized treatment. Yet, it is still an open problem as state-of-the-art algorithms are often not able to process large amounts of data within reasonable time. Furthermore, many of the existing methods predict numerous false positives and have limited capabilities to integrate other sources of information, such as previously known interactions. Here we introduce KBoost, an algorithm that uses kernel PCA regression, boosting and Bayesian model averaging for fast and accurate reconstruction of gene regulatory networks. We have benchmarked KBoost against other high performing algorithms using three different datasets. The results show that our method compares favorably to other methods across datasets. We have also applied KBoost to a large cohort of close to 2000 breast cancer patients and 24,000 genes in less than 2 h on standard hardware. Our results show that molecularly defined breast cancer subtypes also feature differences in their GRNs. An implementation of KBoost in the form of an R package is available at: https://github.com/Luisiglm/KBoost and as a Bioconductor software package.


2021 ◽  
Vol 12 ◽  
Author(s):  
Linzhuo Fan ◽  
Jinhong Hou ◽  
Guimin Qin

Breast cancer is one of the most common malignant tumors in women, which seriously endangers women’s health. Great advances have been made over the last decades, however, most studies predict driver genes of breast cancer using biological experiments and/or computational methods, regardless of stage information. In this study, we propose a computational framework to predict the disease genes of breast cancer based on stage-specific gene regulatory networks. Firstly, we screen out differentially expressed genes and hypomethylated/hypermethylated genes by comparing tumor samples with corresponding normal samples. Secondly, we construct three stage-specific gene regulatory networks by integrating RNA-seq profiles and TF-target pairs, and apply WGCNA to detect modules from these networks. Subsequently, we perform network topological analysis and gene set enrichment analysis. Finally, the key genes of specific modules for each stage are screened as candidate disease genes. We obtain seven stage-specific modules, and identify 20, 12, and 22 key genes for three stages, respectively. Furthermore, 55%, 83%, and 64% of the genes are associated with breast cancer, for example E2F2, E2F8, TPX2, BUB1, and CKAP2L. So it may be of great importance for further verification by cancer experts.


2020 ◽  
Vol 8 (12) ◽  
pp. 85-95
Author(s):  
Francielly Morais Rodrigues da Costa ◽  
Diego Lucas Neres Rodrigues ◽  
Rita Silvério-Machado ◽  
Lucas Gabriel Rodrigues Gomes ◽  
Rodrigo Bentes Kato ◽  
...  

The modified logistic regression (Morais-rodrigues et al., 2020) was used to classify breast cancer subtypes using all microarray database samples. A stabilizing term, that allows the assignment of values to αi∗ parameters, was inserted in this methodology and with that, during the derivation there is the insertion of the identity matrix (positive defined) which added to the other semi-defined part, results in a positive defined matrix, which has auto values > 0 and determinant > 0, square matrix is full rank if it is reversible (determinant > 0) , which results in a single solution. In the results it was observed that some genes were located topologically in the extremities after plotting the parameters αi∗, these parameters are related to the expression of genes with a suppressor or oncogenic profile  in breast cancer, and with genes not studied yet. Some of these genes were found in gene regulatory networks from the search of Iglesias-Martinez et al. (2016), and S-score values were associated with these genes, negative value S-score is indicative of tumor suppressing or reduced gene activity and the positive value S-score is indicative of oncogene or increased gene activity (de Souza et al., 2014). In view of the importance of these genes, this article provides a literary review of them.


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