Identifying biomarkers for breast cancer by gene regulatory network rewiring

被引:10
作者
Wang, Yijuan [1 ]
Liu, Zhi-Ping [1 ]
机构
[1] Shandong Univ, Sch Control Sci & Engn, Dept Biomed Engn, Jinan 250061, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomarker discovery; Gene regulatory network; Network rewiring; Feature selection; Breast cancer; ASSOCIATION; IDENTIFICATION; VALIDATION; DISCOVERY; PROGNOSIS;
D O I
10.1186/s12859-021-04225-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:14
相关论文
共 39 条
  • [1] Robust biomarker identification for cancer diagnosis with ensemble feature selection methods
    Abeel, Thomas
    Helleputte, Thibault
    Van de Peer, Yves
    Dupont, Pierre
    Saeys, Yvan
    [J]. BIOINFORMATICS, 2010, 26 (03) : 392 - 398
  • [2] Rewiring of Genetic Networks in Response to DNA Damage
    Bandyopadhyay, Sourav
    Mehta, Monika
    Kuo, Dwight
    Sung, Min-Kyung
    Chuang, Ryan
    Jaehnig, Eric J.
    Bodenmiller, Bernd
    Licon, Katherine
    Copeland, Wilbert
    Shales, Michael
    Fiedler, Dorothea
    Dutkowski, Janusz
    Guenole, Aude
    van Attikum, Haico
    Shokat, Kevan M.
    Kolodner, Richard D.
    Huh, Won-Ki
    Aebersold, Ruedi
    Keogh, Michael-Christopher
    Krogan, Nevan J.
    Ideker, Trey
    [J]. SCIENCE, 2010, 330 (6009) : 1385 - 1389
  • [3] Widespread Rewiring of Genetic Networks upon Cancer Signaling Pathway Activation
    Billmann, Maximilian
    Chaudhary, Varun
    ElMaghraby, Mostafa F.
    Fischer, Bernd
    Boutros, Michael
    [J]. CELL SYSTEMS, 2018, 6 (01) : 52 - +
  • [4] On variants of shortest-path betweenness centrality and their generic computation
    Brandes, Ulrik
    [J]. SOCIAL NETWORKS, 2008, 30 (02) : 136 - 145
  • [5] [Anonymous], 2020, CA Cancer J Clin, V70, P313, DOI [10.3322/caac.21492, 10.3322/caac.21609]
  • [6] MISS: a non-linear methodology based on mutual information for genetic association studies in both population and sib-pairs analysis
    Brunel, Helena
    Gallardo-Chacon, Joan-Josep
    Buil, Alfonso
    Vallverdu, Montserrat
    Manuel Soria, Jose
    Caminal, Pere
    Perera, Alexandre
    [J]. BIOINFORMATICS, 2010, 26 (15) : 1811 - 1818
  • [7] Butte A J, 2000, Pac Symp Biocomput, P418
  • [8] Chan Y. H., 2005, SMJ Singapore Medical Journal, V46, P259
  • [9] Kinome-wide Decoding of Network-Attacking Mutations Rewiring Cancer Signaling
    Creixell, Pau
    Schoof, Erwin M.
    Simpson, Craig D.
    Longden, James
    Miller, Chad J.
    Lou, Hua Jane
    Perryman, Lara
    Cox, Thomas R.
    Zivanovic, Nevena
    Palmeri, Antonio
    Wesolowska-Andersen, Agata
    Helmer-Citterich, Manuela
    Ferkinghoff-Borg, Jesper
    Itamochi, Hiroaki
    Bodenmiller, Bernd
    Erler, Janine T.
    Turk, Benjamin E.
    Linding, Rune
    [J]. CELL, 2015, 163 (01) : 202 - 217
  • [10] Breast cancer statistics, 2019
    DeSantis, Carol E.
    Ma, Jiemin
    Gaudet, Mia M.
    Newman, Lisa A.
    Miller, Kimberly D.
    Sauer, Ann Goding
    Jemal, Ahmedin
    Siegel, Rebecca L.
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2019, 69 (06) : 438 - 451