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GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL

Primary central nervous system lymphoma (PCNSL) is a brain malignant non-Hodgkin’s B-cell lymphoma. The standard treatments are high-dose methotrexate (MTX)-based chemotherapies and deferred whole brain radiotherapy. However, MTX resistance-dependent global expression and signaling pathway changes a...

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Autores principales: Takashima, Yasuo, Hamano, Momoko, Fukai, Junya, Iwadate, Yasuo, Kajiwara, Koji, Kobayashi, Tsutomu, Hondoh, Hiroaki, Yamanaka, Ryuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242340/
https://www.ncbi.nlm.nih.gov/pubmed/32439996
http://dx.doi.org/10.1038/s41598-020-65463-6
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author Takashima, Yasuo
Hamano, Momoko
Fukai, Junya
Iwadate, Yasuo
Kajiwara, Koji
Kobayashi, Tsutomu
Hondoh, Hiroaki
Yamanaka, Ryuya
author_facet Takashima, Yasuo
Hamano, Momoko
Fukai, Junya
Iwadate, Yasuo
Kajiwara, Koji
Kobayashi, Tsutomu
Hondoh, Hiroaki
Yamanaka, Ryuya
author_sort Takashima, Yasuo
collection PubMed
description Primary central nervous system lymphoma (PCNSL) is a brain malignant non-Hodgkin’s B-cell lymphoma. The standard treatments are high-dose methotrexate (MTX)-based chemotherapies and deferred whole brain radiotherapy. However, MTX resistance-dependent global expression and signaling pathway changes and their relationship with prognoses have not yet been elucidated. Here, we conducted a global expression analysis with next-generation sequencing and gene set enrichment analysis (GSEA) in MTX-resistant PCNSL cell lines (HKBML-MTX and TK-MTX) and PCNSL tissues. In rank scores, genes listed in HKBML-MTX and TK-MTX were enriched in PCNSL with poor prognoses. In fold changes, a part of differentially-expressed genes in PCNSL tissues were also detected in HKBML-MTX and TK-MTX cells; FOXD2-AS1 and MMP19 were commonly expressed in both HKBML-MTX and TK-MTX, FABP5 and CD70 were HKBML-MTX-specifically expressed, and CLCN2, HOXB9, INE1, and LRP5L were TK-MTX-specifically expressed, which may provide a combination of prognostic markers on MTX-sensitivities in PCNSL. Additionally, PCNSL subgroups, divided with hierarchical clustering and Kaplan-Meier methods, included twenty commonly expressed genes in both HKBML-MTX and TK-MTX, ten HKBML-MTX-specifically expressed genes, and two TK-MTX-specifically expressed genes. These results suggest that the GSEA-assisted gene signatures can provide a combination for prognostic markers in recurrent PCNSL with MTX resistances.
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spelling pubmed-72423402020-05-29 GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL Takashima, Yasuo Hamano, Momoko Fukai, Junya Iwadate, Yasuo Kajiwara, Koji Kobayashi, Tsutomu Hondoh, Hiroaki Yamanaka, Ryuya Sci Rep Article Primary central nervous system lymphoma (PCNSL) is a brain malignant non-Hodgkin’s B-cell lymphoma. The standard treatments are high-dose methotrexate (MTX)-based chemotherapies and deferred whole brain radiotherapy. However, MTX resistance-dependent global expression and signaling pathway changes and their relationship with prognoses have not yet been elucidated. Here, we conducted a global expression analysis with next-generation sequencing and gene set enrichment analysis (GSEA) in MTX-resistant PCNSL cell lines (HKBML-MTX and TK-MTX) and PCNSL tissues. In rank scores, genes listed in HKBML-MTX and TK-MTX were enriched in PCNSL with poor prognoses. In fold changes, a part of differentially-expressed genes in PCNSL tissues were also detected in HKBML-MTX and TK-MTX cells; FOXD2-AS1 and MMP19 were commonly expressed in both HKBML-MTX and TK-MTX, FABP5 and CD70 were HKBML-MTX-specifically expressed, and CLCN2, HOXB9, INE1, and LRP5L were TK-MTX-specifically expressed, which may provide a combination of prognostic markers on MTX-sensitivities in PCNSL. Additionally, PCNSL subgroups, divided with hierarchical clustering and Kaplan-Meier methods, included twenty commonly expressed genes in both HKBML-MTX and TK-MTX, ten HKBML-MTX-specifically expressed genes, and two TK-MTX-specifically expressed genes. These results suggest that the GSEA-assisted gene signatures can provide a combination for prognostic markers in recurrent PCNSL with MTX resistances. Nature Publishing Group UK 2020-05-21 /pmc/articles/PMC7242340/ /pubmed/32439996 http://dx.doi.org/10.1038/s41598-020-65463-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Takashima, Yasuo
Hamano, Momoko
Fukai, Junya
Iwadate, Yasuo
Kajiwara, Koji
Kobayashi, Tsutomu
Hondoh, Hiroaki
Yamanaka, Ryuya
GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title_full GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title_fullStr GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title_full_unstemmed GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title_short GSEA-assisted gene signatures valid for combinations of prognostic markers in PCNSL
title_sort gsea-assisted gene signatures valid for combinations of prognostic markers in pcnsl
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242340/
https://www.ncbi.nlm.nih.gov/pubmed/32439996
http://dx.doi.org/10.1038/s41598-020-65463-6
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