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Generation of a monoclonal antibody that inhibits the procoagulant activity of various cancer cell lines
Author(s) -
Inufusa Haruhiko,
Adachi Toshiyuki,
Suzuki Motoyuki,
Ando Osamu,
Ohta Tsunetaka,
Kurimoto Masashi,
Nakatani Yoshihiro,
Nakamura Masato,
Yasutomi Masayuki
Publication year - 1998
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/(sici)1097-0142(19980415)82:8<1563::aid-cncr19>3.0.co;2-2
Subject(s) - tissue factor , monoclonal antibody , cancer cell , cancer , antibody , cell culture , flow cytometry , cancer research , medicine , cell , microbiology and biotechnology , factor vii , immunology , coagulation , biology , biochemistry , genetics
BACKGROUND Tumor procoagulant is one of the factors responsible for disseminated intravascular coagulation and metastasis. The authors found procoagulant activity in LK52 human squamous cell carcinoma cells, which they designated cancer cell‐derived blood coagulating activity 1 (CCA‐1). A monoclonal antibody (MoAb) was generated to characterize this CCA‐1 procoagulant activity. To date, antibodies that show an inhibitory effect on procoagulant activity as well as high reactivity in cancer cells are well known for their tissue factor specificity. METHODS Characterization of the procoagulant activity of CCA‐1 was performed and an anti‐CCA‐1 MoAb, FS01, was generated. CCA‐1 expression on the cancer cell surface was examined by flow cytometry. Procoagulant activity of various cancer cell lines and the inhibitory effect of the FS01 MoAb on this procoagulant activity was monitored by a clot timer. RESULTS The enzymologic character differed from that of cancer procoagulant (CP). The FS01 MoAb inhibited the procoagulant activity of CCA‐1, but did not inhibit that of tissue factor. A positive correlation was observed between the expression intensity of CCA‐1 and the inhibitory effect of the FS01 MoAb on the procoagulant activity of cancer cell lines. Expression of CCA‐l was observed more frequently than that of tissue factor in human cancer cell lines. CONCLUSIONS The FS01 MoAb generated in the current study is a new antibody that reacts with various cancer cell lines, but not with normal cells. FS01 inhibits cancer cell‐derived procoagulant activity and does not react with tissue factor and CP. CCA‐1, which is recognized by the FS01 MoAb, appears to play a major role in cancer cell‐derived procoagulant activity. Cancer 1998;82:1563‐9. © 1998 American Cancer Society.