4.6 Article Proceedings Paper

Identifying biomarkers for breast cancer by gene regulatory network rewiring

期刊

BMC BIOINFORMATICS
卷 22, 期 SUPPL 12, 页码 -

出版社

BMC
DOI: 10.1186/s12859-021-04225-1

关键词

Biomarker discovery; Gene regulatory network; Network rewiring; Feature selection; Breast cancer

资金

  1. National Key Research and Development Program of China [2020YFA0712402]
  2. National Natural Science Foundation of China (NSFC) [61973190, 61572287]
  3. Natural Science Foundation of Shandong Province of China [ZR2020ZD25]
  4. Shandong Provincial Key Research and Development Program (Major Scientific and Technological Innovation Project) [2019JZZY010423]
  5. Program of Qilu Young Scholars of Shandong University
  6. National Key Research and Development Program
  7. NSFC

向作者/读者索取更多资源

The research presents a bioinformatics method for identifying potential biomarkers based on network rewiring in different states. By constructing a differential gene regulatory network (D-GRN) and applying community detection technique, the study successfully selects biomarker genes with the ability to distinguish normal samples from controls.
Background Mining gene regulatory network (GRN) is an important avenue for addressing cancer mechanism. Mutations in cancer genome perturb GRN and cause a rewiring in an orchestrated network. Hence, the exploration of gene regulatory network rewiring is significant to discover potential biomarkers and indicators for discriminating cancer phenotypes. Results Here, we propose a new bioinformatics method of identifying biomarkers based on network rewiring in different states. It firstly reconstructs GRN in different phenotypic conditions from gene expression data with a priori background network. We employ the algorithm based on path consistency algorithm and conditional mutual information to delete false-positive regulatory interactions between independent nodes/genes or not closely related gene pairs. And then a differential gene regulatory network (D-GRN) is constructed from the rewiring parts in the two phenotype-specific GRNs. Community detection technique is then applied for D-GRN to detect functional modules. Finally, we apply logistic regression classifier with recursive feature elimination to select biomarker genes in each module individually. The extracted feature genes result in a gene set of biomarkers with impressing ability to distinguish normal samples from controls. We verify the identified biomarkers in external independent validation datasets. For a proof-of-concept study, we apply the framework to identify diagnostic biomarkers of breast cancer. The identified biomarkers obtain a maximum AUC of 0.985 in the internal sample classification experiments. And these biomarkers achieve a maximum AUC of 0.989 in the external validations. Conclusion In conclusion, network rewiring reveals significant differences between different phenotypes, which indicating cancer dysfunctional mechanisms. With the development of sequencing technology, the amount and quality of gene expression data become available. Condition-specific gene regulatory networks that are close to the real regulations in different states will be established. Revealing the network rewiring will greatly benefit the discovery of biomarkers or signatures for phenotypes. D-GRN is a general method to meet this demand of deciphering the high-throughput data for biomarker discovery. It is also easy to be extended for identifying biomarkers of other complex diseases beyond breast cancer.

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