Loading...
DSCN: Double-target selection guided by CRISPR screening and network
Liu, Enze Wu, Xue Wang, Lei Huo, Yang Li, Lang Cheng, Lijun
Liu, Enze
Wu, Xue
Wang, Lei
Huo, Yang
Li, Lang
Cheng, Lijun
Citations
Altmetric:
Genre
Journal article
Date
2022-08-19
Advisor
Committee member
Group
Department
Health Services Administration and Policy
Permanent link to this record
Collections
Research Projects
Organizational Units
Journal Issue
DOI
http://dx.doi.org/10.1371/journal.pcbi.1009421
Abstract
Cancer is a complex disease with usually multiple disease mechanisms. Target combination is a better strategy than a single target in developing cancer therapies. However, target combinations are generally more difficult to be predicted. Current CRISPR-cas9 technology enables genome-wide screening for potential targets, but only a handful of genes have been screend as target combinations. Thus, an effective computational approach for selecting candidate target combinations is highly desirable. Selected target combinations also need to be translational between cell lines and cancer patients. We have therefore developed DSCN (double-target selection guided by CRISPR screening and network), a method that matches expression levels in patients and gene essentialities in cell lines through spectral-clustered protein-protein interaction (PPI) network. In DSCN, a sub-sampling approach is developed to model first-target knockdown and its impact on the PPI network, and it also facilitates the selection of a second target. Our analysis first demonstrated a high correlation of the DSCN sub-sampling-based gene knockdown model and its predicted differential gene expressions using observed gene expression in 22 pancreatic cell lines before and after MAP2K1 and MAP2K2 inhibition (R2 = 0.75). In DSCN algorithm, various scoring schemes were evaluated. The ‘diffusion-path’ method showed the most significant statistical power of differentialting known synthetic lethal (SL) versus non-SL gene pairs (P = 0.001) in pancreatic cancer. The superior performance of DSCN over existing network-based algorithms, such as OptiCon and VIPER, in the selection of target combinations is attributable to its ability to calculate combinations for any gene pairs, whereas other approaches focus on the combinations among optimized regulators in the network. DSCN’s computational speed is also at least ten times fast than that of other methods. Finally, in applying DSCN to predict target combinations and drug combinations for individual samples (DSCNi), DSCNi showed high correlation between target combinations predicted and real synergistic combinations (P = 1e-5) in pancreatic cell lines. In summary, DSCN is a highly effective computational method for the selection of target combinations.
Description
Citation
Liu E, Wu X, Wang L, Huo Y, Wu H, Li L, et al. (2022) DSCN: Double-target selection guided by CRISPR screening and network. PLoS Comput Biol 18(8): e1009421. https://doi.org/10.1371/journal.pcbi.1009421
Citation to related work
Public Library of Science (PLoS)
Has part
PLoS Computational Biology, Vol. 18
ADA compliance
For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu