Abstract

Boron neutron capture therapy (BNCT) is a high-LET particle radiotherapy clinically tested for treating malignant gliomas. Boronophenylalanine (BPA), a boron-containing phenylalanine derivative, is selectively transported into tumor cells by amino acid transporters, making it an ideal agent for BNCT. In this study, we investigated whether the amino acid 5-aminolevulinic acid (ALA) could sensitize glioma stem cells (GSCs) to BNCT by enhancing the uptake of BPA. Using human and mouse GSC lines, pre-incubation with ALA increased the intracellular accumulation of BPA dose-dependent. We also conducted in vivo experiments by intracerebrally implanting HGG13 cells in mice and administering ALA orally 24 h before BPA administration (ALA + BPA-BNCT). The ALA preloading group increased the tumor boron concentration and improved the tumor/blood boron concentration ratio, resulting in improved survival compared to the BPA-BNCT group. Furthermore, we found that the expression of amino acid transporters was upregulated following ALA treatment both in vitro and in vivo, particularly for ATB0,+. This suggests that ALA may sensitize GSCs to BNCT by upregulating the expression of amino acid transporters, thereby enhancing the uptake of BPA and improving the effectiveness of BNCT. These findings have important implications for strategies to improve the sensitivity of malignant gliomas to BPA-BNCT.

Details

Title
5-Aminolevulinic acid increases boronophenylalanine uptake into glioma stem cells and may sensitize malignant glioma to boron neutron capture therapy
Author
Fukumura, Masao 1 ; Nonoguchi, Naosuke 1 ; Kawabata, Shinji 1 ; Hiramatsu, Ryo 1 ; Futamura, Gen 1 ; Takeuchi, Koji 1 ; Kanemitsu, Takuya 1 ; Takata, Takushi 2 ; Tanaka, Hiroki 2 ; Suzuki, Minoru 2 ; Sampetrean, Oltea 3 ; Ikeda, Naokado 4 ; Kuroiwa, Toshihiko 5 ; Saya, Hideyuki 3 ; Nakano, Ichiro 6 ; Wanibuchi, Masahiko 7 

 Osaka Medical and Pharmaceutical University, Department of Neurosurgery, Takatsuki, Japan 
 Kyoto University, Institute for Integrated Radiation and Nuclear Science, Kumatori, Japan (GRID:grid.258799.8) (ISNI:0000 0004 0372 2033) 
 Keio University School of Medicine, Division of Gene Regulation, Institute for Advanced Medical Research, Tokyo, Japan (GRID:grid.26091.3c) (ISNI:0000 0004 1936 9959) 
 Osaka Medical and Pharmaceutical University, Department of Neurosurgery, Takatsuki, Japan (GRID:grid.26091.3c) 
 Tesseikai Neurosurgical Hospital, Department of Neurosurgery, Shijonawate, Japan (GRID:grid.26091.3c) 
 University of Alabama at Birmingham, Department of Neurosurgery, Birmingham, USA (GRID:grid.265892.2) (ISNI:0000000106344187) 
 Osaka Medical and Pharmaceutical University, Department of Neurosurgery, Takatsuki, Japan (GRID:grid.265892.2) 
Pages
10173
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2828554564
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.