HMOCC-1, a human monoclonal antibody that inhibits adhesion of ovarian cancer cells to human mesothelial cells

Nao Suzuki, Daisuke Aoki, Yutaka Tamada, Nobuyuki Susumu, Kimiko Orikawa, Katsumi Tsukazaki, Motoko Sakayori, Atsushi Suzuki, Takeshi Fukuchi, Makio Mukai, Kyoko Kojima-Aikawa, Isao Ishida, Shiro Nozawa

研究成果: Article査読

17 被引用数 (Scopus)

抄録

Objectives. Ovarian carcinoma is one of the most common gynecologic cancers and shows the worst prognosis since current therapies are not sufficiently effective at achieving and maintaining remission. To develop new treatment, a monoclonal antibody recognizing human ovarian cancer cells was raised in KM mice. Methods. A human monoclonal antibody targeting RMG-I (an ovarian carcinoma cell line) was established with hybridomas of myeloma cells and spleen cells from KM mice. The immunohistochemical reactivity of various types of ovarian carcinoma and other tumors was investigated. RMG-I cells were treated with N-glycosidase F, NaOH, H2SO4, and Gal NAC-α-benzyl to investigate the target antigens by Western blotting. The effect of HMOCC-1 on adhesion of RMG-I cells to cultured human mesothelial cells was also investigated. Results. The new human monoclonal antibody, HMOCC-1, was an immunoglobulin M that recognized ovarian epithelial carcinoma. Immunohistochemical staining revealed HMOCC-1 positivity in 83.2% of ovarian carcinomas. The antigen recognized by HMOCC-1 was apparently a glycoprotein since Western blotting yielded a broad band (34.8-49.1 kDa). HMOCC-1 inhibited the attachment of RMG-I cells to monolayers of cultured peritoneal mesothelial cells in a concentration-dependent manner. Conclusions. This new human monoclonal antibody reacted with most ovarian cancers tested. The antigen recognized by HMOCC-1 is a glycoprotein located on the cell membrane. Inhibition of the attachment of RMG-1 cells to mesothelial cells by HMOCC-1 suggests a potential role for this antibody in the treatment of ovarian cancer.

本文言語English
ページ(範囲)290-298
ページ数9
ジャーナルGynecologic Oncology
95
2
DOI
出版ステータスPublished - 2004 11

ASJC Scopus subject areas

  • 腫瘍学
  • 産婦人科学

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