ArticleBMC systems biology2012
Insights into the pathogenesis of axial spondyloarthropathy from network and pathway analysis.
Article in BMC systems biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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6 citing papers in PubMed, 14 citations in OpenAlex.
- Article
- Observational
- Applications of systems approaches in the study of rheumatic diseases.The Korean journal of internal medicine · 2015Review
- The network organization of cancer-associated protein complexes in human tissues.Scientific reports · 2013Article
- Bioinformatics analysis for the antirheumatic effects of huang-lian-jie-du-tang from a network perspective.Evidence-based complementary and alternative medicine : eCAM · 2013Article
- Therapeutic effects of astragaloside IV on myocardial injuries: multi-target identification and network analysis.PloS one · 2012Article
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Authors and funding
4 authors at 3 institutions in 4 countries.
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Abstract
backgroundComplex chronic diseases are usually not caused by changes in a single causal gene but by an unbalanced regulating network resulting from the dysfunctions of multiple genes or their products. Therefore, network based systems approach can be helpful for the identification of candidate genes related to complex diseases and their relationships. Axial spondyloarthropathy (SpA) is a group of chronic inflammatory joint diseases that mainly affect the spine and the sacroiliac joints. The pathogenesis of SpA remains largely unknown.
resultsIn this paper, we conducted a network study of the pathogenesis of SpA. We integrated data related to SpA, from the OMIM database, proteomics and microarray experiments of SpA, to prioritize SpA candidate disease genes in the context of human protein interactome. Based on the top ranked SpA related genes, we constructed a SpA specific PPI network, identified potential pathways associated with SpA, and finally sketched an overview of biological processes involved in the development of SpA.
conclusionsThe protein-protein interaction (PPI) network and pathways reflect the link between the two pathological processes of SpA, i.e., immune mediated inflammation, as well as imbalanced bone modelling caused new boneformation and bone loss. We found that some known disease causative genes, such as TNFand ILs, play pivotal roles in this interaction.
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