研究者業績

安部 貴大

アベ タカヒロ  (Takahiro Abe)

基本情報

所属
自治医科大学 総合医学第2講座(歯科口腔外科) 教授
学位
博士(医学)(東京大学)

連絡先
abe.takahirojichi.ac.jp
J-GLOBAL ID
200901064825602999
researchmap会員ID
5000100122

研究キーワード

 4

受賞

 1

論文

 56
  • 小松 紀子, 高才 東, 黒田 実可子, 浜窪 隆雄, 安部 貴大
    BIO Clinica 39(11) 975-978 2024年10月  
  • 黒田 実可子, 高才 東, 小松 紀子, 大鶴 光信, 浜窪 隆雄, 安部 貴大
    日本口腔科学会雑誌 73(2) 192-192 2024年9月  
  • 小松 紀子, 黒田 実可子, 高才 東, 沢井 奈津子, 大鶴 光信, 安部 貴大
    日本口腔科学会雑誌 73(2) 207-208 2024年9月  
  • 黒田 実可子, 小松 紀子, 高才 東, 浜窪 隆雄, 安部 貴大
    神奈川歯学 59(抄録集) 35-35 2024年6月  
  • Noriko Komatsu, Azuma Kosai, Mikako Kuroda, Takao Hamakubo, Takahiro Abe
    Biomedicines 12(5) 2024年4月29日  
    BACKGROUND: Photodynamic therapy (PDT) is a cancer-targeted treatment that uses a photosensitizer (PS) and irradiation of a specific wavelength to exert cytotoxic effects. To enhance the antitumor effect against head and neck squamous cell carcinoma (HNSCC), we developed a new phototherapy, intelligent targeted antibody phototherapy (iTAP). This treatment uses a combination of immunotoxin (IT) and a PS for PDT and light irradiation. In our prior study, we demonstrated that an immunotoxin (IT) consisting of an anti-ROBO1 antibody conjugated to saporin, when used in combination with the photosensitizer (PS) disulfonated aluminum phthalocyanine (AlPcS2a) and irradiated with light at the appropriate wavelength, resulted in increased cytotoxicity against head and neck squamous cell carcinoma (HNSCC) cells. ROBO1 is a receptor known to be involved in the progression of cancer. In this study, we newly investigate the iTAP targeting epidermal growth factor receptor (EGFR) which is widely used as a therapeutic target for HNSCC. METHODS: We checked the expression of EGFR in HNSCC cell lines, SAS, HO-1-u-1, Sa3, and HSQ-89. We analyzed the cytotoxicity of saporin-conjugated anti-EGFR antibody (cetuximab) (IT-Cmab), mono-L-aspartyl chlorin e6 (NPe6, talaporfin sodium), and light (664 nm) irradiation (i.e., iTAP) in SAS, HO-1-u-1, Sa3, and HSQ-89 cells. RESULTS: EGFR was expressed highly in Sa3, moderately in HO-1-u-1, SAS, and nearly not in HSQ-89. Cmab alone or IT-Cmab alone did not show cytotoxic effects in Sa3, HO-1-u-1, and HSQ-89 cells, which have moderate or low expression levels of EGFR protein. However, the iTAP method enhanced the cytotoxicity of IT-Cmab by the photodynamic effect in Sa3 and HO-1-u-1 cells, which have moderate levels of EGFR expression. CONCLUSION: Our study is the first to report on the iTAP method using IT-Cmab and NPe6 for HNSCC. The cytotoxic effects are enhanced in cell lines with moderate levels of EGFR protein expression, but not in nonexpressing cell lines, which is expected to expand the range of therapeutic windows and potentially reduce complications.

MISC

 125

講演・口頭発表等

 3

共同研究・競争的資金等の研究課題

 20