Cargando…

TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL

INTRODUCTION: Boron neutron capture therapy (BNCT) is form of tumor-cell selective particle irradiation. Although novel boron compounds have been developed, BPA (boronophenylalanine) and BSH (borocaptate sodium) are used in the clinical practice. The development of effective boron compounds is a maj...

Descripción completa

Detalles Bibliográficos
Autores principales: Fukuo, Yusuke, Kawabata, Shinji, Kashiwagi, Hideki, Kanemitsu, Takuya, Takeuchi, Kouji, Hiramatsu, Ryo, Wanibuchi, Masahiko, Ono, Kouji, Miyatake, Shinichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213153/
http://dx.doi.org/10.1093/noajnl/vdz039.046
_version_ 1783531741491757056
author Fukuo, Yusuke
Kawabata, Shinji
Kashiwagi, Hideki
Kanemitsu, Takuya
Takeuchi, Kouji
Hiramatsu, Ryo
Wanibuchi, Masahiko
Ono, Kouji
Miyatake, Shinichi
author_facet Fukuo, Yusuke
Kawabata, Shinji
Kashiwagi, Hideki
Kanemitsu, Takuya
Takeuchi, Kouji
Hiramatsu, Ryo
Wanibuchi, Masahiko
Ono, Kouji
Miyatake, Shinichi
author_sort Fukuo, Yusuke
collection PubMed
description INTRODUCTION: Boron neutron capture therapy (BNCT) is form of tumor-cell selective particle irradiation. Although novel boron compounds have been developed, BPA (boronophenylalanine) and BSH (borocaptate sodium) are used in the clinical practice. The development of effective boron compounds is a major theme. We used Dodecaborate-containing BPA (AAL) which is combined the characteristics of both BPA and BSH. We have been conducting research on how the new compound for BNCT will affect rat brain tumor model. MATERIALS AND METHODS: We evaluated the boron concentration of F98 glioma cells for BPA and AAL, and the biodistribution of these following BPA administrated intravenously (i.v.) or AAL administrated by convection-enhanced delivery (CED) in F98 glioma bearing rats. In BNCT study, the therapeutic effect was evaluated in terms of the survival time for all rats divided into six groups. RESULTS: The uptake of boron showed almost the same value at all exposure times in high concentration. In biodistribution study, the AAL(CED) 6h after the termination group attained the highest boron concentrations of the tumor (59.9 ± 18.2 μg/g). In the BNCT study, the median survival time in the AAL(CED) group (31(29–35) days) was shorter than that in the BPA(i.v.) group(34(33–36) days). And the combination group of AAL(CED) and BPA(i.v.) gave the most significant prolongation of survival(38(36–40) days). DISCUSSION: AAL(CED) and BPA(i.v.) combined group had a significant survival prolongation compared with the single-agent group. It is thought that AAL irradiated by thermal neutron had a cell-killing effect on cells in which BPA was not taken up. The combination uses of AAL (CED) provides additional BNCT effects. The mechanism by which AAL is incorporated has not been clarified, and further experiments including the influence on normal cells are in progress. CONCLUSION: Dodecaborate-containing BPA (AAL) is a novel boron compound for BNCT that can be expected to prolong the survival time in combination with BPA.
format Online
Article
Text
id pubmed-7213153
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72131532020-07-07 TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL Fukuo, Yusuke Kawabata, Shinji Kashiwagi, Hideki Kanemitsu, Takuya Takeuchi, Kouji Hiramatsu, Ryo Wanibuchi, Masahiko Ono, Kouji Miyatake, Shinichi Neurooncol Adv Abstracts INTRODUCTION: Boron neutron capture therapy (BNCT) is form of tumor-cell selective particle irradiation. Although novel boron compounds have been developed, BPA (boronophenylalanine) and BSH (borocaptate sodium) are used in the clinical practice. The development of effective boron compounds is a major theme. We used Dodecaborate-containing BPA (AAL) which is combined the characteristics of both BPA and BSH. We have been conducting research on how the new compound for BNCT will affect rat brain tumor model. MATERIALS AND METHODS: We evaluated the boron concentration of F98 glioma cells for BPA and AAL, and the biodistribution of these following BPA administrated intravenously (i.v.) or AAL administrated by convection-enhanced delivery (CED) in F98 glioma bearing rats. In BNCT study, the therapeutic effect was evaluated in terms of the survival time for all rats divided into six groups. RESULTS: The uptake of boron showed almost the same value at all exposure times in high concentration. In biodistribution study, the AAL(CED) 6h after the termination group attained the highest boron concentrations of the tumor (59.9 ± 18.2 μg/g). In the BNCT study, the median survival time in the AAL(CED) group (31(29–35) days) was shorter than that in the BPA(i.v.) group(34(33–36) days). And the combination group of AAL(CED) and BPA(i.v.) gave the most significant prolongation of survival(38(36–40) days). DISCUSSION: AAL(CED) and BPA(i.v.) combined group had a significant survival prolongation compared with the single-agent group. It is thought that AAL irradiated by thermal neutron had a cell-killing effect on cells in which BPA was not taken up. The combination uses of AAL (CED) provides additional BNCT effects. The mechanism by which AAL is incorporated has not been clarified, and further experiments including the influence on normal cells are in progress. CONCLUSION: Dodecaborate-containing BPA (AAL) is a novel boron compound for BNCT that can be expected to prolong the survival time in combination with BPA. Oxford University Press 2019-12-16 /pmc/articles/PMC7213153/ http://dx.doi.org/10.1093/noajnl/vdz039.046 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
Fukuo, Yusuke
Kawabata, Shinji
Kashiwagi, Hideki
Kanemitsu, Takuya
Takeuchi, Kouji
Hiramatsu, Ryo
Wanibuchi, Masahiko
Ono, Kouji
Miyatake, Shinichi
TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title_full TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title_fullStr TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title_full_unstemmed TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title_short TB-03 THE SURVIVAL PROLONGATION EFFECT OF NOVEL BORON COMPOUND FOR BNCT USING RAT BRAIN TUMOR MODEL
title_sort tb-03 the survival prolongation effect of novel boron compound for bnct using rat brain tumor model
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213153/
http://dx.doi.org/10.1093/noajnl/vdz039.046
work_keys_str_mv AT fukuoyusuke tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT kawabatashinji tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT kashiwagihideki tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT kanemitsutakuya tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT takeuchikouji tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT hiramatsuryo tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT wanibuchimasahiko tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT onokouji tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel
AT miyatakeshinichi tb03thesurvivalprolongationeffectofnovelboroncompoundforbnctusingratbraintumormodel