1. RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
- Author
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Anton Buzdin, Dmitry Konovalov, R. V. Kholodenko, Daniil Nikitin, Igor Doronin, Denis Kuzmin, Tatyana V. Shamanskaya, Daniel V. Kalinovsky, I. V. Kholodenko, Maxim Sorokin, Aleksei Mironov, and Sergey M. Deyev
- Subjects
medicine.medical_treatment ,ganglioside GD2 ,Medicine (miscellaneous) ,Computational biology ,Ganglioside GD2 Positive ,Biology ,Article ,General Biochemistry, Genetics and Molecular Biology ,Targeted therapy ,molecular diagnostics ,ganglioside biosynthesis ,neuroblastoma ,glioma ,Gene expression ,medicine ,lcsh:QH301-705.5 ,Gene ,Ganglioside ,Cancer ,RNA sequencing ,medicine.disease ,Matthews correlation coefficient ,targeted therapy ,Phenotype ,lcsh:Biology (General) ,NGS ,GD2-positive tumors ,immunotherapy - Abstract
The tumor-associated ganglioside GD2 represents an attractive target for cancer immunotherapy. GD2-positive tumors are more responsive to such targeted therapy, and new methods are needed for the screening of GD2 molecular tumor phenotypes. In this work, we built a gene expression-based binary classifier predicting the GD2-positive tumor phenotypes. To this end, we compared RNA sequencing data from human tumor biopsy material from experimental samples and public databases as well as from GD2-positive and GD2-negative cancer cell lines, for expression levels of genes encoding enzymes involved in ganglioside biosynthesis. We identified a 2-gene expression signature combining ganglioside synthase genes ST8SIA1 and B4GALNT1 that serves as a more efficient predictor of GD2-positive phenotype (Matthews Correlation Coefficient (MCC) 0.32, 0.88, and 0.98 in three independent comparisons) compared to the individual ganglioside biosynthesis genes (MCC 0.02&ndash, 0.32, 0.1&ndash, 0.75, and 0.04&ndash, 1 for the same independent comparisons). No individual gene showed a higher MCC score than the expression signature MCC score in two or more comparisons. Our diagnostic approach can hopefully be applied for pan-cancer prediction of GD2 phenotypes using gene expression data.
- Published
- 2020
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