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RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype

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 class...

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Autores principales: Sorokin, Maxim, Kholodenko, Irina, Kalinovsky, Daniel, Shamanskaya, Tatyana, Doronin, Igor, Konovalov, Dmitry, Mironov, Aleksei, Kuzmin, Denis, Nikitin, Daniil, Deyev, Sergey, Buzdin, Anton, Kholodenko, Roman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344710/
https://www.ncbi.nlm.nih.gov/pubmed/32486168
http://dx.doi.org/10.3390/biomedicines8060142
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author Sorokin, Maxim
Kholodenko, Irina
Kalinovsky, Daniel
Shamanskaya, Tatyana
Doronin, Igor
Konovalov, Dmitry
Mironov, Aleksei
Kuzmin, Denis
Nikitin, Daniil
Deyev, Sergey
Buzdin, Anton
Kholodenko, Roman
author_facet Sorokin, Maxim
Kholodenko, Irina
Kalinovsky, Daniel
Shamanskaya, Tatyana
Doronin, Igor
Konovalov, Dmitry
Mironov, Aleksei
Kuzmin, Denis
Nikitin, Daniil
Deyev, Sergey
Buzdin, Anton
Kholodenko, Roman
author_sort Sorokin, Maxim
collection PubMed
description 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 0.02–0.32, 0.1–0.75, and 0.04–1 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.
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spelling pubmed-73447102020-07-09 RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype Sorokin, Maxim Kholodenko, Irina Kalinovsky, Daniel Shamanskaya, Tatyana Doronin, Igor Konovalov, Dmitry Mironov, Aleksei Kuzmin, Denis Nikitin, Daniil Deyev, Sergey Buzdin, Anton Kholodenko, Roman Biomedicines Article 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 0.02–0.32, 0.1–0.75, and 0.04–1 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. MDPI 2020-05-30 /pmc/articles/PMC7344710/ /pubmed/32486168 http://dx.doi.org/10.3390/biomedicines8060142 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sorokin, Maxim
Kholodenko, Irina
Kalinovsky, Daniel
Shamanskaya, Tatyana
Doronin, Igor
Konovalov, Dmitry
Mironov, Aleksei
Kuzmin, Denis
Nikitin, Daniil
Deyev, Sergey
Buzdin, Anton
Kholodenko, Roman
RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title_full RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title_fullStr RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title_full_unstemmed RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title_short RNA Sequencing-Based Identification of Ganglioside GD2-Positive Cancer Phenotype
title_sort rna sequencing-based identification of ganglioside gd2-positive cancer phenotype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344710/
https://www.ncbi.nlm.nih.gov/pubmed/32486168
http://dx.doi.org/10.3390/biomedicines8060142
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