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Proteomic analysis of cellular response induced by boron neutron capture reaction in human squamous cell carcinoma SAS cells.
Sato, Akira; Itoh, Tasuku; Imamichi, Shoji; Kikuhara, Sota; Fujimori, Hiroaki; Hirai, Takahisa; Saito, Soichiro; Sakurai, Yoshinori; Tanaka, Hiroki; Nakamura, Hiroyuki; Suzuki, Minoru; Murakami, Yasufumi; Baiseitov, Diaz; Berikkhanova, Kulzhan; Zhumadilov, Zhaxybay; Imahori, Yoshio; Itami, Jun; Ono, Koji; Masunaga, Shinichiro; Masutani, Mitsuko.
Afiliação
  • Sato A; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Department of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Japan.
  • Itoh T; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan; Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University o
  • Imamichi S; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan.
  • Kikuhara S; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan; Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University o
  • Fujimori H; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan.
  • Hirai T; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan; Department of Radiation Oncology, Juntendo University, Faculty of Medicine, Japan.
  • Saito S; Division of Genome Stability Research, National Cancer Center Research Institute, Japan.
  • Sakurai Y; Research Reactor Institute, Kyoto University, Japan.
  • Tanaka H; Research Reactor Institute, Kyoto University, Japan.
  • Nakamura H; Chemical Resources Laboratory, Tokyo Institute of Technology, Japan.
  • Suzuki M; Research Reactor Institute, Kyoto University, Japan.
  • Murakami Y; Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Japan.
  • Baiseitov D; Centre for Life Sciences, Nazarbayev University, Kazakhstan.
  • Berikkhanova K; Centre for Life Sciences, Nazarbayev University, Kazakhstan.
  • Zhumadilov Z; Centre for Life Sciences, Nazarbayev University, Kazakhstan.
  • Imahori Y; Cancer Intelligence Care Systems, Inc., Life Sciences Center, Japan.
  • Itami J; Department of Radiation Oncology, National Cancer Center Hospital, Japan.
  • Ono K; Research Reactor Institute, Kyoto University, Japan.
  • Masunaga S; Research Reactor Institute, Kyoto University, Japan.
  • Masutani M; Division of Genome Stability Research, National Cancer Center Research Institute, Japan; Division of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Japan; Department of Frontier Life Sciences, Nagasaki University Graduate School of Biomedical Sciences, Japan; Central
Appl Radiat Isot ; 106: 213-9, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26302661
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Terapia por Captura de Nêutron de Boro / Apoptose / Proteômica / Proteínas de Neoplasias Limite: Humans Idioma: En Revista: Appl Radiat Isot Assunto da revista: MEDICINA NUCLEAR / SAUDE AMBIENTAL Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Terapia por Captura de Nêutron de Boro / Apoptose / Proteômica / Proteínas de Neoplasias Limite: Humans Idioma: En Revista: Appl Radiat Isot Assunto da revista: MEDICINA NUCLEAR / SAUDE AMBIENTAL Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão País de publicação: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM