TY - JOUR
T1 - Integrating knowledge and omics to decipher mechanisms via large-scale models of signaling networks
AU - Garrido-Rodriguez, Martin
AU - Zirngibl, Katharina
AU - Ivanova, Olga
AU - Lobentanzer, Sebastian
AU - Saez-Rodriguez, Julio
N1 - Funding Information: This project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreement No 965193 for DECIDER, German Science Foundation (DFG; Code SA 3554/2‐1 project 411368829 SA 3536/2), and GSK. We thank Pablo R. Mier, Attila Gabor, Daniel Dimitrov, and Jovan Tanevski for fruitful discussions on the content of the manuscript. We also thank Joaquin Dopazo, Robin Browaeys, Josh Stuart, Evan Paull, Emek Demir, Anthony Gitter, Cristoph Bock, and Nikolaus Fortelny for their feedback on the first version of the manuscript. Funding Information: JSR reports funding from GSK and Sanofi and fees from Travere Therapeutics and Astex. Publisher Copyright: © 2022 The Authors. Published under the terms of the CC BY 4.0 license.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Signal transduction governs cellular behavior, and its dysregulation often leads to human disease. To understand this process, we can use network models based on prior knowledge, where nodes represent biomolecules, usually proteins, and edges indicate interactions between them. Several computational methods combine untargeted omics data with prior knowledge to estimate the state of signaling networks in specific biological scenarios. Here, we review, compare, and classify recent network approaches according to their characteristics in terms of input omics data, prior knowledge and underlying methodologies. We highlight existing challenges in the field, such as the general lack of ground truth and the limitations of prior knowledge. We also point out new omics developments that may have a profound impact, such as single-cell proteomics or large-scale profiling of protein conformational changes. We provide both an introduction for interested users seeking strategies to study cell signaling on a large scale and an update for seasoned modelers.
AB - Signal transduction governs cellular behavior, and its dysregulation often leads to human disease. To understand this process, we can use network models based on prior knowledge, where nodes represent biomolecules, usually proteins, and edges indicate interactions between them. Several computational methods combine untargeted omics data with prior knowledge to estimate the state of signaling networks in specific biological scenarios. Here, we review, compare, and classify recent network approaches according to their characteristics in terms of input omics data, prior knowledge and underlying methodologies. We highlight existing challenges in the field, such as the general lack of ground truth and the limitations of prior knowledge. We also point out new omics developments that may have a profound impact, such as single-cell proteomics or large-scale profiling of protein conformational changes. We provide both an introduction for interested users seeking strategies to study cell signaling on a large scale and an update for seasoned modelers.
KW - biological networks
KW - cellular signaling
KW - functional analysis
KW - phosphoproteomics
KW - transcriptomics
UR - http://www.scopus.com/inward/record.url?scp=85135006464&partnerID=8YFLogxK
U2 - https://doi.org/10.15252/msb.202211036
DO - https://doi.org/10.15252/msb.202211036
M3 - Review article
C2 - 35880747
SN - 1744-4292
VL - 18
JO - Molecular systems biology
JF - Molecular systems biology
IS - 7
M1 - e11036
ER -