DRviaSPCN

DRviaSPCN analyzes subpathway (SP) crosstalk networks to prioritize candidate drugs for cancer drug repurposing by integrating SP centrality and enrichment scores of drug- and disease-induced dysfunctional subpathways.


Key Features:

  • R implementation: Implemented as an R package for computational analysis.
  • Subpathway Crosstalk Network Construction: Constructs subpathway (SP) networks that map interactions between cellular pathways relevant to cancer biology.
  • Centrality Score Calculation: Computes centrality scores for SPs to quantify their influence within the crosstalk network.
  • Enrichment Score Analysis: Assesses enrichment scores of drug- and disease-induced dysfunctional SPs and integrates these with centrality scores to prioritize drugs.
  • Weighted Evaluation of Drug–Disease Associations: Evaluates reverse drug–disease associations at a weighted subpathway level to identify repurposing candidates.
  • Identification and Visualization: Identifies potential candidate drugs and provides visualization of SP-level associations for interpretation.

Scientific Applications:

  • Cancer drug repurposing: Prioritizes existing drugs for new cancer indications by linking drug-induced effects to dysfunctional subpathways.
  • Pathway crosstalk analysis: Characterizes pathway interactions that contribute to tumor survival and drug resistance by focusing on SP-level crosstalk.

Methodology:

Construction of a subpathway (SP) network; calculation of SP centrality scores; assessment of enrichment scores for drug- and disease-induced dysfunctional SPs and integration with centrality scores to prioritize drugs; weighted evaluation of drug–disease associations at the subpathway level; and identification and visualization of candidate drugs.

Topics

Details

License:
GPL-3.0
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
11/2/2022
Last Updated:
11/24/2024

Operations

Publications

Wu J, Li X, Wang Q, Han J. DRviaSPCN: a software package for drug repurposing in cancer via a subpathway crosstalk network. Bioinformatics. 2022;38(21):4975-4977. doi:10.1093/bioinformatics/btac611. PMID:36066432.

PMID: 36066432
Funding: - National Natural Science Foundation of China: 62072145 - Natural Science Foundation of Heilongjiang Province: LH2019C042

Links