Capturing functional long non-coding RNAs through integrating large-scale causal relations from gene perturbation experiments

Characterizing functions of long noncoding RNAs (lncRNAs) remains a major challenge, mostly due to the lack of lncRNA-involved regulatory relationships. A wide array of genome-wide expression profiles generated by gene perturbation have been widely used to capture causal links between perturbed gene...

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Veröffentlicht in:EBioMedicine 2018-09, Vol.35, p.369-380
Hauptverfasser: Xu, Jinyuan, Shi, Aiai, Long, Zhilin, Xu, Liwen, Liao, Gaoming, Deng, Chunyu, Yan, Min, Xie, Aiming, Luo, Tao, Huang, Jian, Xiao, Yun, Li, Xia
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Sprache:eng
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Zusammenfassung:Characterizing functions of long noncoding RNAs (lncRNAs) remains a major challenge, mostly due to the lack of lncRNA-involved regulatory relationships. A wide array of genome-wide expression profiles generated by gene perturbation have been widely used to capture causal links between perturbed genes and response genes. Through annotating >600 gene perturbation profiles, over 354,000 causal relationships between perturbed genes and lncRNAs were identified. This large-scale resource of causal relations inspired us to develop a novel computational approach LnCAR for inferring lncRNAs' functions, which showed a higher accuracy than the co-expression based approach. By application of LnCAR to the cancer hallmark processes, we identified 38 lncRNAs involved in distinct carcinogenic processes. The “activating invasion & metastasis” related lncRNAs were strongly associated with metastatic progression in various cancer types and could act as a predictor of cancer metastasis. Meanwhile, the “evading immune destruction” related lncRNAs showed significant associations with immune infiltration of various immune cells and, importantly, can predict response to anti-PD-1 immunotherapy, suggesting their potential roles as biomarkers for immune therapy. Taken together, our approach provides a novel way to systematically reveal functions of lncRNAs, which will be helpful for further experimental exploration and clinical translational research of lncRNAs.
ISSN:2352-3964
2352-3964
DOI:10.1016/j.ebiom.2018.08.050