Cited by 671Bioinformatics and Genomic NetworksGene expression and cancer classificationCancer-related molecular mechanisms research

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MOGONET integrates multi-omics data using graph convolutional networks allowing patient classification and biomarker identification

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Abstract

To fully utilize the advances in omics technologies and achieve a more comprehensive understanding of human diseases, novel computational methods are required for integrative analysis of multiple types of omics data. Here, we present a novel multi-omics integrative method named Multi-Omics Graph cOnvolutional NETworks (MOGONET) for biomedical classification. MOGONET jointly explores omics-specific learning and cross-omics correlation learning for effective multi-omics data classification. We demonstrate that MOGONET outperforms other state-of-the-art supervised multi-omics integrative analysis approaches from different biomedical classification applications using mRNA expression data, DNA methylation data, and microRNA expression data. Furthermore, MOGONET can identify important biomarkers from different omics data types related to the investigated biomedical problems.

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  • Wang et al. proposed the GNN-based MOGONET method for biomedical sample classification and identified subgroup-specific biomarkers.

    “Wang et al. proposed a novel GNN-based method named multi-omics graph convolutional networks (MOGONET) for biomedical sample classification and identified the subgroup-specific biomarkers [113].”

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Research works printed but not linked: 59

  1. Günther, O. P. et al. A computational pipeline for the development of multi-marker bio-signature panels and ensemble classifiers. BMC Bioinform. 13, 326 (2012). · DOI
  2. Kim, D., Li, R., Dudek, S. M. & Ritchie, M. D. Athena: identifying interactions between different levels of genomic data associated with cancer clinical outcomes using grammatical evolution neural network. BioData Min. 6, 23 (2013). · DOI
  3. Singh, A. et al. Diablo: an integrative approach for identifying key molecular drivers from multi-omics assays. Bioinformatics 35, 3055–3062 (2019). · DOI
  4. Sun, Y., Goodison, S., Li, J., Liu, L. & Farmerie, W. Improved breast cancer prognosis through the combination of clinical and genetic markers. Bioinformatics 23, 30–37 (2007). · DOI
  5. Van De Wiel, M. A., Lien, T. G., Verlaat, W., van Wieringen, W. N. & Wilting, S. M. Better prediction by use of co-data: adaptive group-regularized ridge regression. Stat. Med. 35, 368–381 (2016). · DOI
  6. Wang, B. et al. Similarity network fusion for aggregating data types on a genomic scale. Nat. Methods 11, 333–337 (2014). · DOI · Paper page
  7. Shen, R., Olshen, A. B. & Ladanyi, M. Integrative clustering of multiple genomic data types using a joint latent variable model with application to breast and lung cancer subtype analysis. Bioinformatics 25, 2906–2912 (2009). · DOI · Paper page
  8. Kim, D. et al. Knowledge boosting: a graph-based integration approach with multi-omics data and genomic knowledge for cancer clinical outcome prediction. J. Am. Med. Inform. Assoc. 22, 109–120 (2015). · DOI
  9. Tini, G., Marchetti, L., Priami, C. & Scott-Boyer, M.-P. Multi-omics integration-a comparison of unsupervised clustering methodologies. Brief. Bioinform. 20, 1269–1279 (2019). · DOI
  10. Poirion, O. B., Chaudhary, K. & Garmire, L. X. Deep learning data integration for better risk stratification models of bladder cancer. AMIA Summits Transl. Sci. Proc. 2018, 197–206 (2018).
  11. Xie, G. et al. Group lasso regularized deep learning for cancer prognosis from multi-omics and clinical features. Genes 10, 240 (2019). · DOI · Paper page
  12. Parker, J. S. et al. Supervised risk predictor of breast cancer based on intrinsic subtypes. J. Clin. Oncol. 27, 1160–1167 (2009). · DOI
  13. Colaprico, A. et al. Tcgabiolinks: an r/bioconductor package for integrative analysis of tcga data. Nucleic Acids Res. 44, e71–e71 (2016). · DOI
  14. Hodes, R. J. & Buckholtz, N. Accelerating medicines partnership: Alzheimer’s disease (amp-ad) knowledge portal aids alzheimer’s drug discovery through open data sharing. Expert Opin. Ther. Tar. 20, 389–391 (2016). · DOI
  15. A Bennett, D., A Schneider, J., Arvanitakis, Z. & S Wilson, R. Overview and findings from the religious orders study. Curr. Alzheimer Res. 9, 628–645 (2012). · DOI
  16. De Jager, P. L. et al. A multi-omic atlas of the human frontal cortex for aging and alzheimer’s disease research. Sci. Data 5, 180142 (2018). · DOI · Paper page
  17. Jiang, W. et al. Identification of active transcription factor and mirna regulatory pathways in alzheimer’s disease. Bioinformatics 29, 2596–2602 (2013). · DOI
  18. Bihlmeyer, N. A. et al. Novel methods for integration and visualization of genomics and genetics data in alzheimer’s disease. Alzheimer’s Dement. 15, 788–798 (2019). · DOI
  19. Wang, L., Ding, Z., Tao, Z., Liu, Y. & Fu, Y. Generative multi-view human action recognition. In Proceedings of the IEEE International Conference on Computer Vision, 6212–6221 (IEEE, 2019). · DOI
  20. Lê Cao, K.-A., Boitard, S. & Besse, P. Sparse pls discriminant analysis: biologically relevant feature selection and graphical displays for multiclass problems. BMC Bioinform. 12, 253 (2011). · DOI
  21. Chen, J., Bardes, E. E., Aronow, B. J. & Jegga, A. G. Toppgene suite for gene list enrichment analysis and candidate gene prioritization. Nucleic Acids Res. 37, W305–W311 (2009). · DOI · Paper page
  22. Masoumi, J. et al. Apelin, a promising target for Alzheimer disease prevention and treatment. Neuropeptides 70, 76–86 (2018). · DOI
  23. Luo, H., Han, L. & Xu, J. Apelin/apj system: a novel promising target for neurodegenerative diseases. J. Cell. Physiol. 235, 638–657 (2020). · DOI
  24. Kleinz, M. J. & Davenport, A. P. Emerging roles of apelin in biology and medicine. Pharmacol. Ther. 107, 198–211 (2005). · DOI
  25. Luo, H. et al. Apelin-13 suppresses neuroinflammation against cognitive deficit in a streptozotocin-induced rat model of alzheimer’s disease through activation of bdnf-trkb signaling pathway. Front. Pharmacol. 10, 395 (2019). · DOI
  26. Sheng, Z.-H. & Cai, Q. Mitochondrial transport in neurons: impact on synaptic homeostasis and neurodegeneration. Nat. Rev. Neurosci. 13, 77–93 (2012). · DOI
  27. Wang, Q., Tian, J., Chen, H., Du, H. & Guo, L. Amyloid beta-mediated kif5a deficiency disrupts anterograde axonal mitochondrial movement. Neurobiol. Dis. 127, 410–418 (2019). · DOI
  28. Rogers, J. The inflammatory response in alzheimer’s disease. J. Periodontol. 79, 1535–1543 (2008). · DOI
  29. Schreitmüller, B., Laske, C., Stransky, E. & Stellos, K. Increased myeloperoxidase (mpo) plasma levels in patients with alzheimer’s disease. Alzheimer’s Dement. 9, P235–P235 (2013). · DOI
  30. Nagaraj, S. et al. Profile of 6 microrna in blood plasma distinguish early stage Alzheimer’s disease patients from non-demented subjects. Oncotarget 8, 16122–16143 (2017). · DOI
  31. Hohman, T. J., Dumitrescu, L., Cox, N. J. & Jefferson, A. L. Genetic resilience to amyloid related cognitive decline. Brain Imaging Behav. 11, 401–409 (2017). · DOI
  32. Barone, G. et al. Human cdk18 promotes replication stress signaling and genome stability. Nucleic Acids Res. 44, 8772–8785 (2016). · DOI · Paper page
  33. Blows, F. M. et al. Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies. PLoS Med. 7, e1000279 (2010). · DOI
  34. Mohammed, H. et al. Progesterone receptor modulates erα action in breast cancer. Nature 523, 313–317 (2015). · DOI
  35. Wahdan-Alaswad, R., Edgerton, S., Salem, H. & Thor, A. Metformin targets glucose metabolism in triple negative breast cancer. J. Oncol. Transl. Res. 4, 129 (2018). · DOI
  36. Wu, Y. et al. Prosaposin, a regulator of estrogen receptor alpha, promotes breast cancer growth. Cancer Sci. 103, 1820–1825 (2012). · DOI
  37. Castoria, G. et al. Integrating signals between camp and mapk pathways in breast cancer. Front. Biosci. 13, 1318–1327 (2008). · DOI
  38. Muti, P. et al. Fasting glucose is a risk factor for breast cancer: a prospective study. Cancer Epidemiol. Prev. Biomar. 11, 1361–1368 (2002).
  39. Shepherd, J. H. et al. The sox11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression. Oncotarget 7, 13106–13121 (2016). · DOI
  40. Cordero, A. et al. Fabp7 is a key metabolic regulator in her2+ breast cancer brain metastasis. Oncogene 38, 6445–6460 (2019). · DOI
  41. Zhang, H. et al. The proteins fabp7 and oatp2 are associated with the basal phenotype and patient outcome in human breast cancer. Breast Cancer Res. Treat. 121, 41–51 (2010). · DOI
  42. Xiao, Y., Humphries, B., Yang, C. & Wang, Z. Mir-205 dysregulations in breast cancer: the complexity and opportunities. Non-coding RNA 5, 53 (2019). · DOI
  43. Mattie, M. D. et al. Optimized high-throughput microrna expression profiling provides novel biomarker assessment of clinical prostate and breast cancer biopsies. Mol. Cancer 5, 24 (2006). · DOI
  44. Sempere, L. F. et al. Altered microrna expression confined to specific epithelial cell subpopulations in breast cancer. Cancer Res. 67, 11612–11620 (2007). · DOI
  45. Wu, H., Zhu, S. & Mo, Y.-Y. Suppression of cell growth and invasion by mir-205 in breast cancer. Cell Res. 19, 439–448 (2009). · DOI
  46. Iorio, M. V. et al. Microrna gene expression deregulation in human breast cancer. Cancer Res. 65, 7065–7070 (2005). · DOI · Paper page
  47. Mulrane, L. et al. mir-187 is an independent prognostic factor in breast cancer and confers increased invasive potential in vitro. Clin. Cancer Res. 18, 6702–6713 (2012). · DOI
  48. Kipf, T. N. & Welling, M. Semi-supervised classification with graph convolutional networks. In Proceedings of the International Conference on Learning Representations (ICLR, 2017).
  49. Li, Q., Han, Z. & Wu, X.-M. Deeper insights into graph convolutional networks for semi-supervised learning. In Proceedings of the AAAI Conference on Artificial Intelligence (AAAI, 2018). · DOI · Paper page
  50. Xu, B., Shen, H., Cao, Q., Cen, K. & Cheng, X. Graph convolutional networks using heat kernel for semi-supervised learning. In Proceedings of the International Joint Conference on Artificial Intelligence, 1928–1934 (IJCAI, 2019). · DOI
  51. Kipf, T. N. & Welling, M. Variational graph auto-encoders. In Proceedings of the Conference on Neural Information Processing Systems Workshop on Bayesian Deep Learning (NeurIPS, 2016).
  52. Wang, C., Pan, S., Long, G., Zhu, X. & Jiang, J. Mgae: Marginalized graph autoencoder for graph clustering. In Proceedings of the International Conference on Information and Knowledge Management, 889–898 (ACM, 2017). · DOI
  53. Pan, S. et al. Adversarially regularized graph autoencoder for graph embedding. In Proceedings of the International Joint Conference on Artificial Intelligence, 2609–2615 (IJCAI, 2018). · DOI · Paper page
  54. Park, J., Lee, M., Chang, H. J., Lee, K. & Choi, J. Y. Symmetric graph convolutional autoencoder for unsupervised graph representation learning. In Proceedings of the IEEE International Conference on Computer Vision, 6519–6528 (IEEE, 2019). · DOI
  55. Serra, A. et al. Mvda: a multi-view genomic data integration methodology. BMC Bioinform. 16, 261 (2015). · DOI
  56. Zhu, X. et al. Multi-view classification for identification of alzheimer’s disease. In International Workshop on Machine Learning in Medical Imaging, 255–262 (Springer, 2015). · DOI
  57. Li, Y., Wu, F.-X. & Ngom, A. A review on machine learning principles for multi-view biological data integration. Brief. Bioinform. 19, 325–340 (2018).
  58. Setiono, R. & Liu, H. Neural-network feature selector. IEEE Trans. Neural Netw. 8, 654–662 (1997). · DOI
  59. Zhang, G. P. Neural networks for classification: a survey. IEEE Trans. Syst. Man Cybern Part C (Appl. Rev.) 30, 451–462 (2000). · DOI

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Metadata

Authors
Wang, T., Shao, W., Huang, Z., Tang, H., Zhang, J., Ding, Z., & Huang, K.
Affiliations
  • Indiana University Bloomington (US)
  • Indiana University School of Medicine (US)
  • Purdue University West Lafayette (US)
  • Indiana University Indianapolis (US)
  • Tulane University (US)
  • Regenstrief Institute (US)
Corresponding author
  • Ding, Zhengming
  • Huang, Kun
Venue
Nature Communications
Published
2021-06-08
Volume
12
Issue
1
Pages
3445-3445
ISSN
2041-1723 (ISSN-L)
OpenAlex
W3170986249
Cited by
671
References
10
Citations by year
2026: 178 · 2025: 173 · 2024: 150 · 2023: 98 · 2022: 55 · 2021: 15
FWCI
24.96
Type
journal article
Language
en
Open access
Locations
  • Nature Communications (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion, cc-by)
  • Purdue University Indianapolis (Indiana University) (submittedVersion, cc-by)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
U.S. Department of Health & Human Services | NIH | National Institute of Biomedical Imaging and Bioengineering (R01EB025018)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
Keywords
multi-omics integration, graph convolutional networks, patient classification, biomarker discovery, mRNA expression, DNA methylation, microRNA expression, biomedical classification
MeSH terms
Algorithms, Alzheimer Disease, Breast Neoplasms, Female, Humans, Biomarkers, Genomics, Databases, Genetic

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