dBMHCC
dBMHCC compiles curated and predicted hepatocellular carcinoma (HCC)-related phosphorylated biomarkers and associated expression profiles, phosphorylation events, pathways, phosphorylation motifs, protein kinases, and drug interactions to support biomarker discovery and evaluation.
Key Features:
- Extensive Data Repository: Contains 611 HCC-related genes, 234 HCC-associated pathways, 17 phosphorylation motifs linked to 255 protein kinases, 5,955 identified HCC biomarkers, and 1,077 predicted HCC phosphorylated biomarkers (HCCPMs).
- Predictive Platform: Provides a prediction system for identifying new phosphorylated biomarkers and includes an evaluation framework to assess prediction reliability.
- Pathway and Gene Information: Compiles HCC-related pathways and constituent genes as candidate biomarkers for downstream analysis.
- Phosphorylation Evaluation System: Evaluates protein phosphorylation events and their relevance to HCC.
Scientific Applications:
- Biomarker Discovery: Identification and prioritization of phosphorylated biomarkers in HCC, including predicted candidates Methionine adenosyltransferase 2B (MAT2B) and acireductone dioxygenase 1 (ADI1).
- Drug-target Identification: Characterization of drug–target relationships, exemplified by Platelet-derived growth factor receptor alpha (PDGFRA) as a target of Regorafenib.
- Pathway and Mechanism Analysis: Analysis of HCC-associated pathways and constituent genes to investigate mechanisms of HCC progression and therapeutic strategy development.
Methodology:
Prediction of HCC phosphorylated biomarkers and evaluation of protein phosphorylation events using the database's prediction system and phosphorylation evaluation framework.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/18/2021
- Last Updated:
- 2/22/2021
Operations
Publications
Chu Y, Chien C, Sung M, Chen C, Chen Y. dBMHCC: A comprehensive hepatocellular carcinoma (HCC) biomarker database provides a reliable prediction system for novel HCC phosphorylated biomarkers. PLOS ONE. 2020;15(6):e0234084. doi:10.1371/journal.pone.0234084. PMID:32497121. PMCID:PMC7272086.