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SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY

PURPOSE/OBJECTIVE: The molecular responses of glioblastomas (GBMs) to hypofractionated IMRT/TMZ were investigated to elucidate the molecular targets included in the resistance of these tumors to chemo-radiation therapy. MATERIALS /METHODS: Phase I study of neo-adjuvant IMRT (72Gy/12Fx.)/TMZ for the...

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Autores principales: Iuchi, Toshihiko, Hara, Ryusuke, Kageyama, Hajime, Sugiyama, Takahiro, Togasaki, Gentaro, Higuchi, Akio, Hosono, Junji, Setoguchi, Taiki, Hasegawa, Yuzo, Sakaida, Tsukasa, Itami, Makiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213315/
http://dx.doi.org/10.1093/noajnl/vdz039.033
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author Iuchi, Toshihiko
Hara, Ryusuke
Kageyama, Hajime
Sugiyama, Takahiro
Togasaki, Gentaro
Higuchi, Akio
Hosono, Junji
Setoguchi, Taiki
Hasegawa, Yuzo
Sakaida, Tsukasa
Itami, Makiko
author_facet Iuchi, Toshihiko
Hara, Ryusuke
Kageyama, Hajime
Sugiyama, Takahiro
Togasaki, Gentaro
Higuchi, Akio
Hosono, Junji
Setoguchi, Taiki
Hasegawa, Yuzo
Sakaida, Tsukasa
Itami, Makiko
author_sort Iuchi, Toshihiko
collection PubMed
description PURPOSE/OBJECTIVE: The molecular responses of glioblastomas (GBMs) to hypofractionated IMRT/TMZ were investigated to elucidate the molecular targets included in the resistance of these tumors to chemo-radiation therapy. MATERIALS /METHODS: Phase I study of neo-adjuvant IMRT (72Gy/12Fx.)/TMZ for the treatment of patients with GBMs had been performed previously in our institution. In this trial, stereotactic biopsy of the tumor to confirm the pathological diagnosis prior to treatment was required, and tumor removal was scheduled within 10 days after completion of IMRT/TMZ. Therefore, both the tumor samples before and immediately after IMRT/TMZ were available. By comparing the gene expression profiles before and after IMRT/TMZ using the total mRNA sequencing (RNAseq) analysis, molecular responses of GBMs against IMRT/TMZ were investigated. More than two-fold change of expression levels was defined as significant. RESULTS: Tumor sample sets from five patients with GBMs were investigated. Among the 17,532 genes evaluated, 35 genes were found to show significant changes in gene expression in all cases, and 450 genes in more than half of the cases. Among the DNA repair related genes, DDB2 was the only gene that showed significant up-regulation in all cases. On the other hand, among the cell cycle checkpoint related genes, gene expressions of CKD1/CCNB were decreased in all cases. Although the expression of TP53 was not changed, the expressions of CDKN1A/GADD45/Reprimo/SFN were also reduced. Moreover, although the expression change of CHK1 was not found, the expressions of CDC25/PLK1/AURKA were decreased in more than half of the cases. From these results, it was considered that GBM arrested the cell cycle at the G2/M checkpoint without regulation of TP53 or CHK1 after IMRT/TMZ. CONCLUSIONS: Our results suggested that cell cycle arrest in G2/M plays a significant role in survival of GBM cells after IMRT/TMZ.
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spelling pubmed-72133152020-07-07 SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY Iuchi, Toshihiko Hara, Ryusuke Kageyama, Hajime Sugiyama, Takahiro Togasaki, Gentaro Higuchi, Akio Hosono, Junji Setoguchi, Taiki Hasegawa, Yuzo Sakaida, Tsukasa Itami, Makiko Neurooncol Adv Abstracts PURPOSE/OBJECTIVE: The molecular responses of glioblastomas (GBMs) to hypofractionated IMRT/TMZ were investigated to elucidate the molecular targets included in the resistance of these tumors to chemo-radiation therapy. MATERIALS /METHODS: Phase I study of neo-adjuvant IMRT (72Gy/12Fx.)/TMZ for the treatment of patients with GBMs had been performed previously in our institution. In this trial, stereotactic biopsy of the tumor to confirm the pathological diagnosis prior to treatment was required, and tumor removal was scheduled within 10 days after completion of IMRT/TMZ. Therefore, both the tumor samples before and immediately after IMRT/TMZ were available. By comparing the gene expression profiles before and after IMRT/TMZ using the total mRNA sequencing (RNAseq) analysis, molecular responses of GBMs against IMRT/TMZ were investigated. More than two-fold change of expression levels was defined as significant. RESULTS: Tumor sample sets from five patients with GBMs were investigated. Among the 17,532 genes evaluated, 35 genes were found to show significant changes in gene expression in all cases, and 450 genes in more than half of the cases. Among the DNA repair related genes, DDB2 was the only gene that showed significant up-regulation in all cases. On the other hand, among the cell cycle checkpoint related genes, gene expressions of CKD1/CCNB were decreased in all cases. Although the expression of TP53 was not changed, the expressions of CDKN1A/GADD45/Reprimo/SFN were also reduced. Moreover, although the expression change of CHK1 was not found, the expressions of CDC25/PLK1/AURKA were decreased in more than half of the cases. From these results, it was considered that GBM arrested the cell cycle at the G2/M checkpoint without regulation of TP53 or CHK1 after IMRT/TMZ. CONCLUSIONS: Our results suggested that cell cycle arrest in G2/M plays a significant role in survival of GBM cells after IMRT/TMZ. Oxford University Press 2019-12-16 /pmc/articles/PMC7213315/ http://dx.doi.org/10.1093/noajnl/vdz039.033 Text en © The Author(s) 2019. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Iuchi, Toshihiko
Hara, Ryusuke
Kageyama, Hajime
Sugiyama, Takahiro
Togasaki, Gentaro
Higuchi, Akio
Hosono, Junji
Setoguchi, Taiki
Hasegawa, Yuzo
Sakaida, Tsukasa
Itami, Makiko
SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title_full SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title_fullStr SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title_full_unstemmed SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title_short SPDR-09 CHANGES IN CELL CYCLE-RELATED GENE EXPRESSIONS OF GLIOBLASTOMAS BEFORE AND IMMEDIATELY AFTER CHEMO-RADIATION THERAPY
title_sort spdr-09 changes in cell cycle-related gene expressions of glioblastomas before and immediately after chemo-radiation therapy
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213315/
http://dx.doi.org/10.1093/noajnl/vdz039.033
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