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Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients
The human c‐erbB‐2 protooncogene product (erbB‐2 protein) is a 185 kilodalton glycoprotein closely related to epidermal growth factor receptor protein. In this study, we measured the concentration of circulating erbB‐2 protein in cancer patients by means of a new immunoradiometric assay (IRMA). Two...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1993
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919131/ https://www.ncbi.nlm.nih.gov/pubmed/8096502 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02848.x |
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author | Hosono, Makoto Saga, Tsuneo Sakahara, Harumi Kobayashi, Hisataka Shirato, Makoto Endo, Keigo Yamamoto, Tadashi Akiyama, Tetsu Toyoshima, Kumao Konishi, Junji |
author_facet | Hosono, Makoto Saga, Tsuneo Sakahara, Harumi Kobayashi, Hisataka Shirato, Makoto Endo, Keigo Yamamoto, Tadashi Akiyama, Tetsu Toyoshima, Kumao Konishi, Junji |
author_sort | Hosono, Makoto |
collection | PubMed |
description | The human c‐erbB‐2 protooncogene product (erbB‐2 protein) is a 185 kilodalton glycoprotein closely related to epidermal growth factor receptor protein. In this study, we measured the concentration of circulating erbB‐2 protein in cancer patients by means of a new immunoradiometric assay (IRMA). Two monoclonal antibodies (MoAbs), SV2‐61γ and 6G10, recognize erbB‐2 protein but bind to separate epitopes. SV2‐61γ was used as an immunoadsorbent and 6G10 as an (125)I‐labeled probe. A serum was considered positive for erbB‐2 protein if the percent binding exceeded the mean of the normal group by more than 3 standard deviations. Eleven of 21 patients with advanced breast cancer and 1 of 15 with advanced gastric cancer were positive. Serum erbB‐2 protein levels correlated well with the therapy and the status of the patients with breast cancer. On the contrary, all patients with advanced colon, ovarian, or pancreatic cancers, showed levels below the cut‐off value. These results suggest that circulating erbB‐2 protein can be measured using the newly constructed IRMA. Since c‐erbB‐2 protooncogene amplification and overexpression are accepted as a good marker of aggressiveness, relapsing potency, and poor prognosis, this IRMA should be a promising tool with which to help manage breast cancer patients. |
format | Online Article Text |
id | pubmed-5919131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59191312018-05-11 Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients Hosono, Makoto Saga, Tsuneo Sakahara, Harumi Kobayashi, Hisataka Shirato, Makoto Endo, Keigo Yamamoto, Tadashi Akiyama, Tetsu Toyoshima, Kumao Konishi, Junji Jpn J Cancer Res Article The human c‐erbB‐2 protooncogene product (erbB‐2 protein) is a 185 kilodalton glycoprotein closely related to epidermal growth factor receptor protein. In this study, we measured the concentration of circulating erbB‐2 protein in cancer patients by means of a new immunoradiometric assay (IRMA). Two monoclonal antibodies (MoAbs), SV2‐61γ and 6G10, recognize erbB‐2 protein but bind to separate epitopes. SV2‐61γ was used as an immunoadsorbent and 6G10 as an (125)I‐labeled probe. A serum was considered positive for erbB‐2 protein if the percent binding exceeded the mean of the normal group by more than 3 standard deviations. Eleven of 21 patients with advanced breast cancer and 1 of 15 with advanced gastric cancer were positive. Serum erbB‐2 protein levels correlated well with the therapy and the status of the patients with breast cancer. On the contrary, all patients with advanced colon, ovarian, or pancreatic cancers, showed levels below the cut‐off value. These results suggest that circulating erbB‐2 protein can be measured using the newly constructed IRMA. Since c‐erbB‐2 protooncogene amplification and overexpression are accepted as a good marker of aggressiveness, relapsing potency, and poor prognosis, this IRMA should be a promising tool with which to help manage breast cancer patients. Blackwell Publishing Ltd 1993-02 /pmc/articles/PMC5919131/ /pubmed/8096502 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02848.x Text en |
spellingShingle | Article Hosono, Makoto Saga, Tsuneo Sakahara, Harumi Kobayashi, Hisataka Shirato, Makoto Endo, Keigo Yamamoto, Tadashi Akiyama, Tetsu Toyoshima, Kumao Konishi, Junji Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title | Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title_full | Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title_fullStr | Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title_full_unstemmed | Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title_short | Construction of Immunoradiometric Assay for Circulating c‐erbB‐2 Protooncogene Product in Advanced Breast Cancer Patients |
title_sort | construction of immunoradiometric assay for circulating c‐erbb‐2 protooncogene product in advanced breast cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919131/ https://www.ncbi.nlm.nih.gov/pubmed/8096502 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02848.x |
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