| Literature DB >> 31178611 |
Yang Ni1, Francesco C Stingo2, Min Jin Ha3, Rehan Akbani4, Veerabhadran Baladandayuthapani3.
Abstract
Identifying patient-specific prognostic biomarkers is of critical importance in developing personalized treatment for clinically and molecularly heterogeneous diseases such as cancer. In this article, we propose a novel regression framework, Bayesian hierarchical varying-sparsity regression (BEHAVIOR) models to select clinically relevant disease markers by integrating proteogenomic (proteomic+genomic) and clinical data. Our methods allow flexible modeling of protein-gene relationships as well as induces sparsity in both protein-gene and protein-survival relationships, to select ge-nomically driven prognostic protein markers at the patient-level. Simulation studies demonstrate the superior performance of BEHAVIOR against competing method in terms of both protein marker selection and survival prediction. We apply BEHAV-IOR to The Cancer Genome Atlas (TCGA) proteogenomic pan-cancer data and find several interesting prognostic proteins and pathways that are shared across multiple cancers and some that exclusively pertain to specific cancers.Entities:
Keywords: Prognostic biomarker; p-splines; precision medicine; threshold; tumor heterogeneity
Year: 2018 PMID: 31178611 PMCID: PMC6552682 DOI: 10.1080/01621459.2018.1434529
Source DB: PubMed Journal: J Am Stat Assoc ISSN: 0162-1459 Impact factor: 5.033