Predicting Molecular Subtypes of Breast Cancer Using Gene Expression Profiling and Random Forest Classifier

Background: One of the main causes of cancer-related mortality in women is breast cancer [BC]. There were four molecular subtypes of this malignancy, and adjuvant therapy efficacy differed based on these subtypes. Gene expression profiles provide valuable information that is helpful for patients whose prognosis is not clear from clinical markers and immunohistochemistry. Objective: In this study, we aim to predict molecular types of BC using a gene expression dataset of patients with BC and normal samples using six well-known ensemble machine-learning techniques. Methods: Two microarray datasets were downloaded; [GSE45827] and [GSE140494] from the Gene Expression Omnibus [GEO] database. These datasets comprise 21 samples of normal tissues that were part of a cohort analysis of primary invasive breast cancer [57 basal, 36 HER2, 56 Luminal A, and 66 Luminal B]. Namely, we used AdaBoost, Random Forest [RF], Artificial Neural Network [ANN], Naïve Bayes [NB], Classification and Regression Tree [CART], and Linear Discriminant Analysis [LDA] classifiers. Results: The results of the data analysis show that the RF and NB classifiers outperform the other models in the prediction of the BC subtype. The RF shows superior performance with an accuracy range between 0.89 and 1.0 in contrast to its competitor NB, which has an average accuracy of 0.91. Our approach perfectly discriminates un-affected cases [normal] from the carcinoma. In this case, the RF provides perfect prediction with zero errors. Additionally, we used PCA, DHWT lowfrequency, and DHWT high-frequency to perform a dimensional reduction for the numerous gene expression values. Consequently, the LDA achieves up to 95% improvement in performance through data reduction. Moreover, feature selection allowed for the best performance, which is recorded by the RF with classification accuracy 98%. Conclusion: Overall, we provide a successful framework that leads to shorter computation times and smaller ML models, especially where memory and time restrictions are crucial.

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Publication Details

Journal
Current Bioinformatics
Published
2024-10-11
DOI
https://doi.org/10.2174/0115748936314079240827062219
Citations
1
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
0.23
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article

Predicting Molecular Subtypes of Breast Cancer Using Gene Expression Profiling and Random Forest Classifier

Ahmad B. Hassanat, Enas Al-khlifeh, Abdulfattah Fararjeh, Abdulaziz A. Aloliqi et al.
1 citations
Current Bioinformatics
Gene expression and cancer classification
0.23
article

Predicting Molecular Subtypes of Breast Cancer Using Gene Expression Profiling and Random Forest Classifier

Ahmad B. Hassanat, Enas Al-khlifeh, Abdulfattah Fararjeh, Abdulaziz A. Aloliqi, Ahmad S. Tarawneh
article en
1 citations

Abstract

Background: One of the main causes of cancer-related mortality in women is breast cancer [BC]. There were four molecular subtypes of this malignancy, and adjuvant therapy efficacy differed based on these subtypes. Gene expression profiles provide valuable information that is helpful for patients whose prognosis is not clear from clinical markers and immunohistochemistry. Objective: In this study, we aim to predict molecular types of BC using a gene expression dataset of patients with BC and normal samples using six well-known ensemble machine-learning techniques. Methods: Two microarray datasets were downloaded; [GSE45827] and [GSE140494] from the Gene Expression Omnibus [GEO] database. These datasets comprise 21 samples of normal tissues that were part of a cohort analysis of primary invasive breast cancer [57 basal, 36 HER2, 56 Luminal A, and 66 Luminal B]. Namely, we used AdaBoost, Random Forest [RF], Artificial Neural Network [ANN], Naïve Bayes [NB], Classification and Regression Tree [CART], and Linear Discriminant Analysis [LDA] classifiers. Results: The results of the data analysis show that the RF and NB classifiers outperform the other models in the prediction of the BC subtype. The RF shows superior performance with an accuracy range between 0.89 and 1.0 in contrast to its competitor NB, which has an average accuracy of 0.91. Our approach perfectly discriminates un-affected cases [normal] from the carcinoma. In this case, the RF provides perfect prediction with zero errors. Additionally, we used PCA, DHWT lowfrequency, and DHWT high-frequency to perform a dimensional reduction for the numerous gene expression values. Consequently, the LDA achieves up to 95% improvement in performance through data reduction. Moreover, feature selection allowed for the best performance, which is recorded by the RF with classification accuracy 98%. Conclusion: Overall, we provide a successful framework that leads to shorter computation times and smaller ML models, especially where memory and time restrictions are crucial.

Current BioinformaticsVol. 20(10)
Qassim University (SA), Mutah University (JO), Al-Balqa Applied University (JO)
Reduced inequalities
Openalex Percentile: Top 42%
Gene expression and cancer classification
0.23
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