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Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer
BACKGROUND: RAI3 is an orphan G-protein coupled receptor (GPCR) that has been associated with malignancy and may play a role in the proliferation of breast cancer cells. Although its exact function in normal and malignant cells remains unclear and evidence supporting its role in oncogenesis is contr...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711971/ https://www.ncbi.nlm.nih.gov/pubmed/19552806 http://dx.doi.org/10.1186/1471-2407-9-200 |
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author | Jörißen, Hannah Bektas, Nuran Dahl, Edgar Hartmann, Arndt ten Haaf, Anette Di Fiore, Stefano Kiefer, Hans Thess, Andreas Barth, Stefan Klockenbring, Torsten |
author_facet | Jörißen, Hannah Bektas, Nuran Dahl, Edgar Hartmann, Arndt ten Haaf, Anette Di Fiore, Stefano Kiefer, Hans Thess, Andreas Barth, Stefan Klockenbring, Torsten |
author_sort | Jörißen, Hannah |
collection | PubMed |
description | BACKGROUND: RAI3 is an orphan G-protein coupled receptor (GPCR) that has been associated with malignancy and may play a role in the proliferation of breast cancer cells. Although its exact function in normal and malignant cells remains unclear and evidence supporting its role in oncogenesis is controversial, its abundant expression on the surface of cancer cells would make it an interesting target for the development of antibody-based therapeutics. To investigate the link with cancer and provide more evidence for its role, we carried out a systematic analysis of RAI3 expression in a large set of human breast cancer specimens. METHODS: We expressed recombinant human RAI3 in bacteria and reconstituted the purified protein in liposomes to raise monoclonal antibodies using classical hybridoma techniques. The specific binding activity of the antibodies was confirmed by enzyme-linked immunosorbent assay (ELISA), western blot and immunocytochemistry. We carried out a systematic immunohistochemical analysis of RAI3 expression in human invasive breast carcinomas (n = 147) and normal breast tissues (n = 44) using a tissue microarray. In addition, a cDNA dot blot hybridisation assay was used to investigate a set of matched normal and cancerous breast tissue specimens (n = 50) as well as lymph node metastases (n = 3) for RAI3 mRNA expression. RESULTS: The anti-RAI3 monoclonal antibodies bound to recombinant human RAI3 protein with high specificity and affinity, as shown by ELISA, western blot and ICC. The cDNA dot blot and immunohistochemical experiments showed that both RAI3 mRNA and RAI3 protein were abundantly expressed in human breast carcinoma. However, there was no association between RAI3 protein expression and prognosis based on overall and recurrence-free survival. CONCLUSION: We have generated a novel, highly-specific monoclonal antibody that detects RAI3 in formaldehyde-fixed paraffin-embedded tissue. This is the first study to report a systematic analysis of RAI3 expression in normal and cancerous human breast tissue at both the mRNA and protein levels. |
format | Text |
id | pubmed-2711971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27119712009-07-17 Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer Jörißen, Hannah Bektas, Nuran Dahl, Edgar Hartmann, Arndt ten Haaf, Anette Di Fiore, Stefano Kiefer, Hans Thess, Andreas Barth, Stefan Klockenbring, Torsten BMC Cancer Technical Advance BACKGROUND: RAI3 is an orphan G-protein coupled receptor (GPCR) that has been associated with malignancy and may play a role in the proliferation of breast cancer cells. Although its exact function in normal and malignant cells remains unclear and evidence supporting its role in oncogenesis is controversial, its abundant expression on the surface of cancer cells would make it an interesting target for the development of antibody-based therapeutics. To investigate the link with cancer and provide more evidence for its role, we carried out a systematic analysis of RAI3 expression in a large set of human breast cancer specimens. METHODS: We expressed recombinant human RAI3 in bacteria and reconstituted the purified protein in liposomes to raise monoclonal antibodies using classical hybridoma techniques. The specific binding activity of the antibodies was confirmed by enzyme-linked immunosorbent assay (ELISA), western blot and immunocytochemistry. We carried out a systematic immunohistochemical analysis of RAI3 expression in human invasive breast carcinomas (n = 147) and normal breast tissues (n = 44) using a tissue microarray. In addition, a cDNA dot blot hybridisation assay was used to investigate a set of matched normal and cancerous breast tissue specimens (n = 50) as well as lymph node metastases (n = 3) for RAI3 mRNA expression. RESULTS: The anti-RAI3 monoclonal antibodies bound to recombinant human RAI3 protein with high specificity and affinity, as shown by ELISA, western blot and ICC. The cDNA dot blot and immunohistochemical experiments showed that both RAI3 mRNA and RAI3 protein were abundantly expressed in human breast carcinoma. However, there was no association between RAI3 protein expression and prognosis based on overall and recurrence-free survival. CONCLUSION: We have generated a novel, highly-specific monoclonal antibody that detects RAI3 in formaldehyde-fixed paraffin-embedded tissue. This is the first study to report a systematic analysis of RAI3 expression in normal and cancerous human breast tissue at both the mRNA and protein levels. BioMed Central 2009-06-24 /pmc/articles/PMC2711971/ /pubmed/19552806 http://dx.doi.org/10.1186/1471-2407-9-200 Text en Copyright ©2009 Jörißen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Advance Jörißen, Hannah Bektas, Nuran Dahl, Edgar Hartmann, Arndt ten Haaf, Anette Di Fiore, Stefano Kiefer, Hans Thess, Andreas Barth, Stefan Klockenbring, Torsten Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title | Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title_full | Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title_fullStr | Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title_full_unstemmed | Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title_short | Production and characterisation of monoclonal antibodies against RAI3 and its expression in human breast cancer |
title_sort | production and characterisation of monoclonal antibodies against rai3 and its expression in human breast cancer |
topic | Technical Advance |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711971/ https://www.ncbi.nlm.nih.gov/pubmed/19552806 http://dx.doi.org/10.1186/1471-2407-9-200 |
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