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Published on: August 25, 2023
Drug Normalization for Cancer Therapeutic and Druggable Genome Target Discovery
Guoqian Jiang1, Sunghwan Sohn1, Michael T Zimmermann1
1Department of Health Sciences Research, Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN.
Abstract:
Heterogeneous drug data representation among different druggable genome knowledge resources and datasets delays effective cancer therapeutic target discovery within the broad scientific community. The objective of the present paper is to describe the challenges and lessons learned from our efforts in developing and evaluating a standards-based drug normalization framework targeting cancer druggable genome datasets. Our findings suggested that mechanisms need to be established to deal with spelling errors and irregularities in normalizing clinical drug data in The Cancer Genome Atlas (TCGA), whereas the annotations from NCI Thesaurus (NCIt) and PubChem are two layers of normalization that potentially bridge between the clinical phenotypes and the druggable genome knowledge for effective cancer therapeutic target discovery.
Insights
Standardizing cancer drug data is crucial for discovering new therapies. Our framework addresses data inconsistencies in resources like The Cancer Genome Atlas (TCGA), improving target discovery.
Area of Science:
- Bioinformatics
- Genomics
- Pharmacology
Background:
- Drug data is represented heterogeneously across knowledge resources, hindering cancer therapeutic target discovery.
- Standardization is needed to integrate diverse datasets for effective drug development.
Purpose of the Study:
- To describe challenges and lessons learned in developing a standards-based drug normalization framework.
- To evaluate this framework for cancer druggable genome datasets.
Main Methods:
- Development of a standards-based drug normalization framework.
- Evaluation of the framework using cancer druggable genome datasets.
- Analysis of data from The Cancer Genome Atlas (TCGA), NCI Thesaurus (NCIt), and PubChem.
Main Results:
- Identified the need for mechanisms to handle spelling errors and irregularities in clinical drug data (e.g., TCGA).
- Demonstrated that NCIt and PubChem annotations serve as crucial normalization layers.
- Showcased the potential of these layers to bridge clinical phenotypes and druggable genome knowledge.
Conclusions:
- A standards-based approach is essential for normalizing heterogeneous drug data.
- Effective normalization facilitates the integration of clinical and genomic data for cancer target discovery.
- NCIt and PubChem provide valuable layers for bridging phenotypes and druggable targets.
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