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Generation of metastatic melanoma specific antibodies by affinity purification

Melanoma is the most aggressive type of skin cancer and one of the most frequent tumours in young adults. Identification of primary tumours prone to develop metastasis is of paramount importance for further patient stratification. However, till today, no markers exist that are routinely used to pred...

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Autores principales: Schütz, Birgit, Koppensteiner, Anita, Schörghofer, David, Kinslechner, Katharina, Timelthaler, Gerald, Eferl, Robert, Hengstschläger, Markus, Missbichler, Albert, Hundsberger, Harald, Mikula, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112778/
https://www.ncbi.nlm.nih.gov/pubmed/27853253
http://dx.doi.org/10.1038/srep37253
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author Schütz, Birgit
Koppensteiner, Anita
Schörghofer, David
Kinslechner, Katharina
Timelthaler, Gerald
Eferl, Robert
Hengstschläger, Markus
Missbichler, Albert
Hundsberger, Harald
Mikula, Mario
author_facet Schütz, Birgit
Koppensteiner, Anita
Schörghofer, David
Kinslechner, Katharina
Timelthaler, Gerald
Eferl, Robert
Hengstschläger, Markus
Missbichler, Albert
Hundsberger, Harald
Mikula, Mario
author_sort Schütz, Birgit
collection PubMed
description Melanoma is the most aggressive type of skin cancer and one of the most frequent tumours in young adults. Identification of primary tumours prone to develop metastasis is of paramount importance for further patient stratification. However, till today, no markers exist that are routinely used to predict melanoma progression. To ameliorate this problem, we generated antiserum directed against metastatic melanoma tissue lysate and applied a novel approach to purify the obtained serum via consecutive affinity chromatography steps. The established antibody, termed MHA-3, showed high reactivity against metastatic melanoma cell lines both in vitro and in vivo. We also tested MHA-3 on 227 melanoma patient samples and compared staining with the melanoma marker S100b. Importantly, MHA-3 was able to differentiate between metastatic and non-metastatic melanoma samples. By proteome analysis we identified 18 distinct antigens bound by MHA-3. Combined expression profiling of all identified proteins revealed a significant survival difference in melanoma patients. In conclusion, we developed a polyclonal antibody, which is able to detect metastatic melanoma on paraffin embedded sections. Hence, we propose that this antibody will represent a valuable additional tool for precise melanoma diagnosis.
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spelling pubmed-51127782016-11-25 Generation of metastatic melanoma specific antibodies by affinity purification Schütz, Birgit Koppensteiner, Anita Schörghofer, David Kinslechner, Katharina Timelthaler, Gerald Eferl, Robert Hengstschläger, Markus Missbichler, Albert Hundsberger, Harald Mikula, Mario Sci Rep Article Melanoma is the most aggressive type of skin cancer and one of the most frequent tumours in young adults. Identification of primary tumours prone to develop metastasis is of paramount importance for further patient stratification. However, till today, no markers exist that are routinely used to predict melanoma progression. To ameliorate this problem, we generated antiserum directed against metastatic melanoma tissue lysate and applied a novel approach to purify the obtained serum via consecutive affinity chromatography steps. The established antibody, termed MHA-3, showed high reactivity against metastatic melanoma cell lines both in vitro and in vivo. We also tested MHA-3 on 227 melanoma patient samples and compared staining with the melanoma marker S100b. Importantly, MHA-3 was able to differentiate between metastatic and non-metastatic melanoma samples. By proteome analysis we identified 18 distinct antigens bound by MHA-3. Combined expression profiling of all identified proteins revealed a significant survival difference in melanoma patients. In conclusion, we developed a polyclonal antibody, which is able to detect metastatic melanoma on paraffin embedded sections. Hence, we propose that this antibody will represent a valuable additional tool for precise melanoma diagnosis. Nature Publishing Group 2016-11-17 /pmc/articles/PMC5112778/ /pubmed/27853253 http://dx.doi.org/10.1038/srep37253 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schütz, Birgit
Koppensteiner, Anita
Schörghofer, David
Kinslechner, Katharina
Timelthaler, Gerald
Eferl, Robert
Hengstschläger, Markus
Missbichler, Albert
Hundsberger, Harald
Mikula, Mario
Generation of metastatic melanoma specific antibodies by affinity purification
title Generation of metastatic melanoma specific antibodies by affinity purification
title_full Generation of metastatic melanoma specific antibodies by affinity purification
title_fullStr Generation of metastatic melanoma specific antibodies by affinity purification
title_full_unstemmed Generation of metastatic melanoma specific antibodies by affinity purification
title_short Generation of metastatic melanoma specific antibodies by affinity purification
title_sort generation of metastatic melanoma specific antibodies by affinity purification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112778/
https://www.ncbi.nlm.nih.gov/pubmed/27853253
http://dx.doi.org/10.1038/srep37253
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