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.

PMID: 32497121
PMCID: PMC7272086
Funding: - Ministry of Science and Technology, Taiwan: 108-2321-B-005- 008, 108-2634-F-005 -002, 109-2320-B-039 -005, MOST 106-2313-B-005-035-MY2 - National Chung Hsing University and Chung-Shan Medical University: NCHU-CSMU-10811