癌症研究
结合
抗体
癌症
癌细胞
硼
中子俘获
化学
医学
免疫学
内科学
数学
数学分析
有机化学
作者
Ikuhiko Nakase,Naoki Takemura,Yuriko Ito Sakai,Shiori Hirase,Miki Ishimura,Tomoka Takatani‐Nakase,Yoshihide Hattori,Mitsunori Kirihata
出处
期刊:ACS omega
[American Chemical Society]
日期:2020-09-02
卷期号:5 (36): 22731-22738
被引量:31
标识
DOI:10.1021/acsomega.0c01377
摘要
Boron neutron capture therapy (BNCT) is a radiation method used for cancer therapy. Cellular uptake of boron-10 (10B) atoms induces cancer cell death by the generation of alpha particles and recoiling lithium-7 (7Li) nuclei when the cells are irradiated with low-energy thermal neutrons. Current BNCT technology shows effective therapeutic benefits in refractory cancers such as brain tumors and head and neck cancers. However, improvements to cancer targeting and the cellular uptake efficacy of the boron compounds and the expansion of the diseases treatable by BNCT are highly desirable. In this research, we aimed to develop an antibody-based drug delivery method for BNCT through the use of the Z33 peptide, which shows specific recognition of and interaction with the Fc domain of human IgG, for on-demand receptor targeting. In addition, we determined with an in vitro assay that macropinocytosis induction during antibody-based drug delivery is crucial for the biological activity of BNCT.
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