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A novel monoclonal antibody targeting coxsackie virus and adenovirus receptor inhibits tumor growth in vivo.
Kawada, Manabu; Inoue, Hiroyuki; Kajikawa, Masunori; Sugiura, Masahito; Sakamoto, Shuichi; Urano, Sakiko; Karasawa, Chigusa; Usami, Ihomi; Futakuchi, Mitsuru; Masuda, Tohru.
Afiliação
  • Kawada M; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, 18-24 Miyamoto, Numazu-shi, Shizuoka 410-0301, Japan.
  • Inoue H; Institute of Microbial Chemistry (BIKAKEN), Laboratory of Oncology, Microbial Chemistry Research Foundation, 3-14-23 Kamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan.
  • Kajikawa M; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, 18-24 Miyamoto, Numazu-shi, Shizuoka 410-0301, Japan.
  • Sugiura M; Medical &Biological Laboratories Co., Ltd., 4-5-3 Sakae, Naka-ku, Nagoya, Aichi 460-0008, Japan.
  • Sakamoto S; Medical &Biological Laboratories Co., Ltd., 4-5-3 Sakae, Naka-ku, Nagoya, Aichi 460-0008, Japan.
  • Urano S; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, 18-24 Miyamoto, Numazu-shi, Shizuoka 410-0301, Japan.
  • Karasawa C; Medical &Biological Laboratories Co., Ltd., 4-5-3 Sakae, Naka-ku, Nagoya, Aichi 460-0008, Japan.
  • Usami I; Medical &Biological Laboratories Co., Ltd., 4-5-3 Sakae, Naka-ku, Nagoya, Aichi 460-0008, Japan.
  • Futakuchi M; Institute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, 18-24 Miyamoto, Numazu-shi, Shizuoka 410-0301, Japan.
  • Masuda T; Department of Molecular Toxicology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.
Sci Rep ; 7: 40400, 2017 01 11.
Article em En | MEDLINE | ID: mdl-28074864
ABSTRACT
To create a new anti-tumor antibody, we conducted signal sequence trap by retrovirus-meditated expression method and identified coxsackie virus and adenovirus receptor (CXADR) as an appropriate target. We developed monoclonal antibodies against human CXADR and found that one antibody (6G10A) significantly inhibited the growth of subcutaneous as well as orthotopic xenografts of human prostate cancer cells in vivo. Furthermore, 6G10A also inhibited other cancer xenografts expressing CXADR, such as pancreatic and colorectal cancer cells. Knockdown and overexpression of CXADR confirmed the dependence of its anti-tumor activity on CXADR expression. Our studies of its action demonstrated that 6G10A exerted its anti-tumor activity primarily through both antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. Moreover, 6G10A reacted with human tumor tissues, such as prostate, lung, and brain, each of which express CXADR. Although we need further evaluation of its reactivity and safety in human tissues, our results show that a novel anti-CXADR antibody may be a feasible candidate for cancer immunotherapy.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína de Membrana Semelhante a Receptor de Coxsackie e Adenovirus / Anticorpos Monoclonais Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína de Membrana Semelhante a Receptor de Coxsackie e Adenovirus / Anticorpos Monoclonais Limite: Animals / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article