OncoPPi
OncoPPi maps cancer-associated protein-protein interactions (PPIs) by integrating genomic, pharmacological, clinical, and structural data to identify oncogenic PPIs and potential therapeutic targets.
Key Features:
- High-Throughput Screening Platform: Detects PPIs associated with cancer using a high-throughput experimental screening framework focused on cancer cell contexts.
- Experimental Validation in Cancer Cells: Provides experimentally validated interaction data derived from assays performed in cancer cell lines.
- Comprehensive Data Integration: Integrates genomic alterations, cellular co-localization, domain-domain interactions, pharmacological data, clinical annotations, and structural evidence into the PPI network.
- Mutual Exclusivity Analysis: Analyzes mutual exclusivity of genomic alterations across interacting proteins to inform oncogenic relationships.
- Therapeutic Connectivity Analysis: Links PPI networks with therapeutic data to highlight potential drug targets and connections between interactome components and treatments.
Scientific Applications:
- Discovery of New Biological Models: Elucidates novel PPIs involved in cancer to support development of mechanistic biological models of tumorigenesis.
- Identification of Therapeutic Targets: Maps oncogenic PPI networks to aid in pinpointing candidate targets for drug development and precision oncology.
- Understanding Oncogenic Signaling Pathways: Characterizes cancer-specific interactomes to reveal dysregulated signaling pathways driving cancer progression.
Methodology:
Applies data integration strategies combining genomic, pharmacological, clinical, and structural data and performs computational analysis of mutual exclusivity of genomic alterations and interaction parameters.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/9/2020
- Last Updated:
- 1/4/2021
Operations
Data Inputs & Outputs
Publications
Ivanov AA. Explore Protein–Protein Interactions for Cancer Target Discovery Using the OncoPPi Portal. Methods in Molecular Biology. 2019. doi:10.1007/978-1-4939-9873-9_12. PMID:31583637.
PMID: 31583637