'N-of-1-pathways' unveils personal deregulated mechanisms from a single pair of RNA-Seq samples: towards precision medicine

被引:28
作者
Gardeux, Vincent [1 ,2 ,3 ,4 ]
Achour, Ikbel [1 ,2 ,4 ]
Li, Jianrong [1 ,2 ,4 ]
Maienschein-Cline, Mark [4 ]
Li, Haiquan [1 ,2 ,4 ]
Pesce, Lorenzo [5 ,6 ]
Parinandi, Gurunadh [2 ,4 ]
Bahroos, Neil [4 ]
Winn, Robert [2 ,7 ]
Foster, Ian [5 ,6 ,8 ,9 ]
Garcia, Joe G. N. [1 ]
Lussier, Yves A. [1 ,2 ,4 ,5 ,7 ,10 ,11 ,12 ,13 ]
机构
[1] Univ Arizona, Dept Med, Inst Bio5, UA Canc Ctr, Tucson, AZ 85721 USA
[2] Univ Illinois, Dept Med, Chicago, IL USA
[3] EISTI, Dept Med, Sch Engn, Cergy Pontoise, France
[4] Univ Illinois, Inst Translat Hlth Informat, Chicago, IL USA
[5] Argonne Natl Lab, Computat Inst, Chicago, IL USA
[6] Univ Chicago, Chicago, IL 60637 USA
[7] Univ Chicago, Ctr Canc, Chicago, IL 60637 USA
[8] Univ Chicago, Dept Comp Sci, Chicago, IL 60637 USA
[9] Argonne Natl Lab, Math & Comp Sci Div, Chicago, IL USA
[10] Univ Illinois, Dept Bioengn, Chicago, IL USA
[11] Univ Illinois, Coll Pharm, Dept Biopharmaceut Sci, Chicago, IL USA
[12] Univ Chicago, Inst Genom & Syst Biol, Chicago, IL 60637 USA
[13] Univ Illinois, Dept Pharmacol, Chicago, IL USA
关键词
GENOME-WIDE ASSOCIATION; LUNG ADENOCARCINOMA; CLINICAL-TRIALS; CANCER; CLASSIFICATION; DISEASE; BREAST; MICROARRAYS; EXPRESSION; PREDICTION;
D O I
10.1136/amiajnl-2013-002519
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Background The emergence of precision medicine allowed the incorporation of individual molecular data into patient care. Indeed, DNA sequencing predicts somatic mutations in individual patients. However, these genetic features overlook dynamic epigenetic and phenotypic response to therapy. Meanwhile, accurate personal transcriptome interpretation remains an unmet challenge. Further, N-of-1 (single-subject) efficacy trials are increasingly pursued, but are underpowered for molecular marker discovery. Method 'N-of-1-pathways' is a global framework relying on three principles: (i) the statistical universe is a single patient; (ii) significance is derived from geneset/biomodules powered by paired samples from the same patient; and (iii) similarity between genesets/biomodules assesses commonality and differences, within-study and cross-studies. Thus, patient gene-level profiles are transformed into deregulated pathways. From RNA-Seq of 55 lung adenocarcinoma patients, N-of-1-pathways predicts the deregulated pathways of each patient. Results Cross-patient N-of-1-pathways obtains comparable results with conventional genesets enrichment analysis (GSEA) and differentially expressed gene (DEG) enrichment, validated in three external evaluations. Moreover, heatmap and star plots highlight both individual and shared mechanisms ranging from molecular to organ-systems levels (eg, DNA repair, signaling, immune response). Patients were ranked based on the similarity of their deregulated mechanisms to those of an independent gold standard, generating unsupervised clusters of diametric extreme survival phenotypes (p= 0.03). Conclusions The N-of-1-pathways framework provides a robust statistical and relevant biological interpretation of individual disease-free survival that is often overlooked in conventional cross-patient studies. It enables mechanism-level classifiers with smaller cohorts as well as N-of-1 studies.
引用
收藏
页码:1015 / 1025
页数:11
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