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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7242340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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