Authors: Akira Sato,Tasuku Itoh,Shoji Imamichi,Sota Kikuhara,Hiroaki Fujimori,Takahisa Hirai,Soichiro Saito,Yoshinori Sakurai,Hiroki Tanaka,Hiroyuki Nakamura,Minoru Suzuki,Yasufumi Murakami,Diaz Baiseitov,Kulzhan Berikkhanova,Zhaxybay Zhumadilov,Yoshio Imahori,Jun Itami,Koji Ono,Shinichiro Masunaga,Mitsuko Masutani,
Journal: Applied Radiation and Isotopes
https://doi.org/10.1016/j.apradiso.2015.08.001
Abstract: To understand the mechanism of cell death induced by boron neutron capture reaction (BNCR), we performed proteome analyses of human squamous tumor SAS cells after BNCR. Cells were irradiated with thermal neutron beam at KUR after incubation under boronophenylalanine (BPA)(+) and BPA(−) conditions. BNCR mainly induced typical apoptosis in SAS cells 24h post-irradiation. Proteomic analysis in SAS cells suggested that proteins functioning in endoplasmic reticulum, DNA repair, and RNA processing showed dynamic changes at early phase after BNCR and could be involved in the regulation of cellular response to BNCR. We found that the BNCR induces fragments of endoplasmic reticulum-localized lymphoid-restricted protein (LRMP). The fragmentation of LRMP was also observed in the rat tumor graft model 20 hours after BNCT treatment carried out at the National Nuclear Center of the Republic of Kazakhstan. These data suggest that dynamic changes of LRMP could be involved during cellular response to BNCR.
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Proteomic analysis of cellular response induced by boron neutron capture reaction in human squamous cell carcinoma SAS cells
Applied Radiation and Isotopes, 2015