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A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II)
A cell line designated RMG‐II was established from the ascites of a patient with ovarian clear cell carcinoma. The chromosomal analysis revealed aneuploidy with a hypertetraploid modal numher and 8 marker chromosomes. Radioimmunoassay and immunocytochemical staining showed that RMG‐II cells produced...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1991
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918546/ https://www.ncbi.nlm.nih.gov/pubmed/1715339 http://dx.doi.org/10.1111/j.1349-7006.1991.tb02713.x |
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author | Nozawa, Shiro Yajima, Masazumi Sasaki, Hirosuke Tsukazaki, Katsumi Aoki, Daisuke Sakayori, Motoko Udagawa, Yasuhiro Kobayashi, Toshifumi Sato, Ichiro Furusako, Shoji Mochizuki, Hiroshi |
author_facet | Nozawa, Shiro Yajima, Masazumi Sasaki, Hirosuke Tsukazaki, Katsumi Aoki, Daisuke Sakayori, Motoko Udagawa, Yasuhiro Kobayashi, Toshifumi Sato, Ichiro Furusako, Shoji Mochizuki, Hiroshi |
author_sort | Nozawa, Shiro |
collection | PubMed |
description | A cell line designated RMG‐II was established from the ascites of a patient with ovarian clear cell carcinoma. The chromosomal analysis revealed aneuploidy with a hypertetraploid modal numher and 8 marker chromosomes. Radioimmunoassay and immunocytochemical staining showed that RMG‐II cells produced some tumor markers such as CA125 and TPA. Two monoclonal antibodies, designated MA602‐1 and MA602‐6, were generated by immunization of mice with an extract prepared from the culture supernatant of RMG‐II cells. The epitopes recognized by these two monoclonal antibodies were proved to differ from the CA125 epitope, but to exist on the molecule bearing CA125. We developed a double‐determinant sandwich enzyme imnnmoassay using these two monoclonal anti‐bodies, and the antigen defined by this assay was termed CA602. CA602 was frequently found in the sera of ovarian cancer patients; the positive rates were 92%, 38%, 60%, and 80% for serous, mucinous, clear cell, and endometrioid ovarian carcinomas, respectively, when the cut‐off value was set at 60 U/ml (=mean + 3SD of healthy females). CA602 levels in serum were also high in endometriosis patients and in early pregnancy, as is the case for CA125, and the correlation coefficient between CA602 and CA125 was high (r=0.88). Our preliminary evidence suggests that this CA602 assay system has higher sensitivity than the CA125 one. |
format | Online Article Text |
id | pubmed-5918546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59185462018-05-11 A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) Nozawa, Shiro Yajima, Masazumi Sasaki, Hirosuke Tsukazaki, Katsumi Aoki, Daisuke Sakayori, Motoko Udagawa, Yasuhiro Kobayashi, Toshifumi Sato, Ichiro Furusako, Shoji Mochizuki, Hiroshi Jpn J Cancer Res Article A cell line designated RMG‐II was established from the ascites of a patient with ovarian clear cell carcinoma. The chromosomal analysis revealed aneuploidy with a hypertetraploid modal numher and 8 marker chromosomes. Radioimmunoassay and immunocytochemical staining showed that RMG‐II cells produced some tumor markers such as CA125 and TPA. Two monoclonal antibodies, designated MA602‐1 and MA602‐6, were generated by immunization of mice with an extract prepared from the culture supernatant of RMG‐II cells. The epitopes recognized by these two monoclonal antibodies were proved to differ from the CA125 epitope, but to exist on the molecule bearing CA125. We developed a double‐determinant sandwich enzyme imnnmoassay using these two monoclonal anti‐bodies, and the antigen defined by this assay was termed CA602. CA602 was frequently found in the sera of ovarian cancer patients; the positive rates were 92%, 38%, 60%, and 80% for serous, mucinous, clear cell, and endometrioid ovarian carcinomas, respectively, when the cut‐off value was set at 60 U/ml (=mean + 3SD of healthy females). CA602 levels in serum were also high in endometriosis patients and in early pregnancy, as is the case for CA125, and the correlation coefficient between CA602 and CA125 was high (r=0.88). Our preliminary evidence suggests that this CA602 assay system has higher sensitivity than the CA125 one. Blackwell Publishing Ltd 1991-07 /pmc/articles/PMC5918546/ /pubmed/1715339 http://dx.doi.org/10.1111/j.1349-7006.1991.tb02713.x Text en |
spellingShingle | Article Nozawa, Shiro Yajima, Masazumi Sasaki, Hirosuke Tsukazaki, Katsumi Aoki, Daisuke Sakayori, Motoko Udagawa, Yasuhiro Kobayashi, Toshifumi Sato, Ichiro Furusako, Shoji Mochizuki, Hiroshi A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title | A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title_full | A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title_fullStr | A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title_full_unstemmed | A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title_short | A New CA125‐like Antigen (CA602) Recognized by Two Monoclonal Antibodies against a Newly Established Ovarian Clear Cell Carcinoma Cell Line (RMG‐II) |
title_sort | new ca125‐like antigen (ca602) recognized by two monoclonal antibodies against a newly established ovarian clear cell carcinoma cell line (rmg‐ii) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918546/ https://www.ncbi.nlm.nih.gov/pubmed/1715339 http://dx.doi.org/10.1111/j.1349-7006.1991.tb02713.x |
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