A novel approach to predicting the synergy of anti-cancer drug combinations using document-based feature extraction
Yongsun Shim1, Munhwan Lee1, Pil-Jong Kim2
1Biomedical Knowledge Engineering, Seoul National University, Seoul, Republic of Korea.
Background:
To reduce drug side effects and enhance their therapeutic effect compared with single drugs, drug combination research, combining two or more drugs, is highly important. Conducting in-vivo and in-vitro experiments on a vast number of drug combinations incurs astronomical time and cost. To reduce the number of combinations, researchers classify whether drug combinations are synergistic through in-silico methods. Since unstructured data, such as biomedical documents, include experimental types, methods, and results, it can be beneficial extracting features from documents to predict anti-cancer drug combination synergy. However, few studies predict anti-cancer drug combination synergy using document-extracted features.
Results:
We present a novel approach for anti-cancer drug combination synergy prediction using document-based feature extraction. Our approach is divided into two steps. First, we extracted documents containing validated anti-cancer drug combinations and cell lines. Drug and cell line synonyms in the extracted documents were converted into representative words, and the documents were preprocessed by tokenization, lemmatization, and stopword removal. Second, the drug and cell line features were extracted from the preprocessed documents, and training data were constructed by feature concatenation. A prediction model based on deep and machine learning was created using the training data. The use of our features yielded higher results compared to the majority of published studies.
Conclusions:
Using our prediction model, researchers can save time and cost on new anti-cancer drug combination discoveries. Additionally, since our feature extraction method does not require structuring of unstructured data, new data can be immediately applied without any data scalability issues.
Insights
This study introduces a new computational method to predict anti-cancer drug combination synergy by extracting features from biomedical documents. This approach reduces experimental costs and time for discovering effective drug combinations.
Area of Science:
- Computational biology
- Bioinformatics
- Drug discovery
Background:
- Drug combination research is crucial for enhancing therapeutic effects and reducing side effects compared to single drugs.
- In-silico methods are vital for predicting drug synergy, but few studies utilize features extracted from unstructured biomedical documents.
- High costs and time associated with in-vivo and in-vitro experiments necessitate efficient prediction models.
Purpose of the Study:
- To develop a novel approach for predicting anti-cancer drug combination synergy.
- To leverage document-extracted features for predicting drug synergy, addressing limitations of existing methods.
- To reduce the time and cost associated with identifying effective anti-cancer drug combinations.
Main Methods:
- A two-step approach involving document extraction and feature engineering.
- Preprocessing of biomedical documents, including synonym conversion, tokenization, lemmatization, and stopword removal.
- Extraction of drug and cell line features from preprocessed documents, followed by feature concatenation to build training data for deep and machine learning models.
Main Results:
- The developed prediction model, utilizing document-extracted features, achieved superior performance compared to most published studies.
- The approach successfully extracted relevant features from unstructured biomedical text data.
- The model demonstrated high accuracy in predicting anti-cancer drug combination synergy.
Conclusions:
- The prediction model significantly saves time and resources in the discovery of new anti-cancer drug combinations.
- The feature extraction method is adaptable to new data without requiring data structuring, overcoming scalability issues.
- This approach facilitates faster and more cost-effective drug discovery pipelines.
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