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pmid:35052318
Artificial Intelligence Analysis of Gene Expression Predicted the Overall Survival of Mantle Cell Lymphoma and a Large Pan-Cancer Series.
Joaquim Carreras · Naoya Nakamura · Rifat Hamoudi
Healthcare (Basel, Switzerland) · 2022 doi:10.3390/healthcare10010155
Paper
complete
Experiment
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Data
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Analysis
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Execution
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Complete file
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An algorithm using multilayer perceptron artificial neural network, radial basis function, gene set enrichment analysis (GSEA), and conventional statistics, correlated 20,862 genes with 28 MCL prognostic genes for dimensionality reduction, to predict the patients' overall survival and highlight new markers. As a result, 58 genes predicted survival with high accuracy (area under the curve = 0.9). Further reduction identified 10 genes: KIF18A, YBX3, PEMT, GCNA, and POGLUT3 that associated with a poor survival; and SELENOP, AMOTL2, IGFBP7, KCTD12, and ADGRG2 with a favorable survival. Correlation with the proliferation index (Ki67) was also made. Interestingly, these genes, which were related to cell cycle, apoptosis, and metabolism, also predicted the survival of diffuse large B-cell lymphoma (GSE10846, n = 414), and a pan-cancer series of The Cancer Genome Atlas (TCGA, n = 7289), which included the most relevant cancers (lung, breast, colorectal, prostate, stomach, liver, etcetera). Secondly, survival was predicted using 10 oncology panels (transcriptome, cancer progression and pathways, metabolic pathways, immuno-oncology, and host response), and TYMS was highlighted. Finally, using machine learning, C5 tree and Bayesian network had the highest accuracy for prediction and correlation with the LLMPP MCL35 proliferation assay and RGS1 was made. 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Correlation with the proliferation index (Ki67) was also made. Interestingly, these genes,", "ng (Figure 11, Figure 12 and Figure 13), and immunohistochemistry for RGS1 (Figure 14). Overall survival in a", "(arrows). Overall survival according to the immunohistochemical expression of RGS1. 2.5.2. Algorithm Based o", "thods 1 and 2 with the MCL35 signature. 3.7. 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