Cargando…
A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin
Podoplanin (PDPN/Aggrus/T1α), a platelet aggregation-inducing mucin-like sialoglycoprotein, is highly expressed in many cancers and normal tissues. A neutralizing monoclonal antibody (mAb; NZ-1) can block the association between podoplanin and C-type lectin-like receptor-2 (CLEC-2) and inhibit podop...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118152/ https://www.ncbi.nlm.nih.gov/pubmed/25080943 http://dx.doi.org/10.1038/srep05924 |
_version_ | 1782328793560514560 |
---|---|
author | Kato, Yukinari Kaneko, Mika Kato |
author_facet | Kato, Yukinari Kaneko, Mika Kato |
author_sort | Kato, Yukinari |
collection | PubMed |
description | Podoplanin (PDPN/Aggrus/T1α), a platelet aggregation-inducing mucin-like sialoglycoprotein, is highly expressed in many cancers and normal tissues. A neutralizing monoclonal antibody (mAb; NZ-1) can block the association between podoplanin and C-type lectin-like receptor-2 (CLEC-2) and inhibit podoplanin-induced cancer metastasis, but NZ-1 reacts with podoplanin-expressing normal cells such as lymphatic endothelial cells. In this study, we established a cancer-specific mAb (CasMab) against human podoplanin. Aberrantly glycosylated podoplanin including keratan sulfate or aberrant sialylation, which was expressed in LN229 glioblastoma cells, was used as an immunogen. The newly established LpMab-2 mAb recognized both an aberrant O-glycosylation and a Thr55-Leu64 peptide from human podoplanin. Because LpMab-2 reacted with podoplanin-expressing cancer cells but not with normal cells, as shown by flow cytometry and immunohistochemistry, it is an anti-podoplanin CasMab that is expected to be useful for molecular targeting therapy against podoplanin-expressing cancers. |
format | Online Article Text |
id | pubmed-4118152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41181522014-08-15 A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin Kato, Yukinari Kaneko, Mika Kato Sci Rep Article Podoplanin (PDPN/Aggrus/T1α), a platelet aggregation-inducing mucin-like sialoglycoprotein, is highly expressed in many cancers and normal tissues. A neutralizing monoclonal antibody (mAb; NZ-1) can block the association between podoplanin and C-type lectin-like receptor-2 (CLEC-2) and inhibit podoplanin-induced cancer metastasis, but NZ-1 reacts with podoplanin-expressing normal cells such as lymphatic endothelial cells. In this study, we established a cancer-specific mAb (CasMab) against human podoplanin. Aberrantly glycosylated podoplanin including keratan sulfate or aberrant sialylation, which was expressed in LN229 glioblastoma cells, was used as an immunogen. The newly established LpMab-2 mAb recognized both an aberrant O-glycosylation and a Thr55-Leu64 peptide from human podoplanin. Because LpMab-2 reacted with podoplanin-expressing cancer cells but not with normal cells, as shown by flow cytometry and immunohistochemistry, it is an anti-podoplanin CasMab that is expected to be useful for molecular targeting therapy against podoplanin-expressing cancers. Nature Publishing Group 2014-08-01 /pmc/articles/PMC4118152/ /pubmed/25080943 http://dx.doi.org/10.1038/srep05924 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kato, Yukinari Kaneko, Mika Kato A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title | A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title_full | A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title_fullStr | A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title_full_unstemmed | A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title_short | A Cancer-specific Monoclonal Antibody Recognizes the Aberrantly Glycosylated Podoplanin |
title_sort | cancer-specific monoclonal antibody recognizes the aberrantly glycosylated podoplanin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118152/ https://www.ncbi.nlm.nih.gov/pubmed/25080943 http://dx.doi.org/10.1038/srep05924 |
work_keys_str_mv | AT katoyukinari acancerspecificmonoclonalantibodyrecognizestheaberrantlyglycosylatedpodoplanin AT kanekomikakato acancerspecificmonoclonalantibodyrecognizestheaberrantlyglycosylatedpodoplanin AT katoyukinari cancerspecificmonoclonalantibodyrecognizestheaberrantlyglycosylatedpodoplanin AT kanekomikakato cancerspecificmonoclonalantibodyrecognizestheaberrantlyglycosylatedpodoplanin |