Identification of human age-associated gene co-expressions in functional modules using liquid association

Aging is a major risk factor for age-related diseases such as certain cancers. In this study, we developed Age Associated Gene Co-expression Identifier (AAGCI), a liquid association based method to infer age-associated gene co-expressions at thousands of biological processes and pathways across 9 hu...

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Veröffentlicht in:Oncotarget 2018-01, Vol.9 (1), p.1063-1074
Hauptverfasser: Yang, Jialiang, Qin, Yufang, Zhang, Tiantian, Wang, Fayou, Peng, Lihong, Zhu, Lijuan, Yuan, Dawei, Gao, Pan, Zhuang, Jujuan, Zhang, Zhongyang, Wang, Jun, Fang, Yun
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Sprache:eng
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Zusammenfassung:Aging is a major risk factor for age-related diseases such as certain cancers. In this study, we developed Age Associated Gene Co-expression Identifier (AAGCI), a liquid association based method to infer age-associated gene co-expressions at thousands of biological processes and pathways across 9 human tissues. Several hundred to thousands of gene pairs were inferred to be age co-expressed across different tissues, the genes involved in which are significantly enriched in functions like immunity, ATP binding, DNA damage, and many cancer pathways. The age co-expressed genes are significantly overlapped with aging genes curated in the GenAge database across all 9 tissues, suggesting a tissue-wide correlation between age-associated genes and co-expressions. Interestingly, age-associated gene co-expressions are significantly different from gene co-expressions identified through correlation analysis, indicating that aging might only contribute to a small portion of gene co-expressions. Moreover, the key driver analysis identified biologically meaningful genes in important function modules. For example, were inferred to be key genes driving age co-expressed genes in the network module associated with function "T cell proliferation". Finally, we prioritized a few anti-aging drugs such as metformin based on an enrichment analysis between age co-expressed genes and drug signatures from a recent study. The predicted drugs were partially validated by literature mining and can be readily used to generate hypothesis for further experimental validations.
ISSN:1949-2553
1949-2553
DOI:10.18632/oncotarget.23148