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A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma
Matriptase is a transmembrane serine protease, synthesized as an inactive single-chain zymogen on the endoplasmic reticulum and transported to the plasma membrane. Matriptase is activated in different epithelial and some B-cell malignancies and changes its conformation and activity is inhibited main...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467949/ https://www.ncbi.nlm.nih.gov/pubmed/31024856 http://dx.doi.org/10.3389/fonc.2019.00258 |
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author | Rather, Gulam M. Lin, Siang-Yo Lin, Hongxia Szekely, Zoltan Bertino, Joseph R. |
author_facet | Rather, Gulam M. Lin, Siang-Yo Lin, Hongxia Szekely, Zoltan Bertino, Joseph R. |
author_sort | Rather, Gulam M. |
collection | PubMed |
description | Matriptase is a transmembrane serine protease, synthesized as an inactive single-chain zymogen on the endoplasmic reticulum and transported to the plasma membrane. Matriptase is activated in different epithelial and some B-cell malignancies and changes its conformation and activity is inhibited mainly by its endogenous inhibitor HAI-1. Activated matriptase plays a key role in tumor initiation as well as tumor progression, including invasiveness, and metastasis. To target the anti-mitotic toxin (monomethyl auristatin-E) to activated matriptase, a novel antibody to activated matriptase was conjugated with this toxin via a valine-citrulline-PABA linker. In a previous study, this antibody-toxin conjugate was found to be effective against triple negative breast cancer cell lines and xenografts, alone, or in combination with cisplatin (1). In this study, we examined the anti-tumor effect of the antibody toxin conjugate (ADC) against activated matriptase positive mantle cell lymphoma cell lines (JeKo-1, Maver, Mino, and Z138). This ADC was cytotoxic to these cell lines with IC(50)s between 5 and 14 μg/mL. The ADC also showed a dose dependent anti-tumor effect on the JeKo-1 xenograft in mice without toxicity. |
format | Online Article Text |
id | pubmed-6467949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64679492019-04-25 A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma Rather, Gulam M. Lin, Siang-Yo Lin, Hongxia Szekely, Zoltan Bertino, Joseph R. Front Oncol Oncology Matriptase is a transmembrane serine protease, synthesized as an inactive single-chain zymogen on the endoplasmic reticulum and transported to the plasma membrane. Matriptase is activated in different epithelial and some B-cell malignancies and changes its conformation and activity is inhibited mainly by its endogenous inhibitor HAI-1. Activated matriptase plays a key role in tumor initiation as well as tumor progression, including invasiveness, and metastasis. To target the anti-mitotic toxin (monomethyl auristatin-E) to activated matriptase, a novel antibody to activated matriptase was conjugated with this toxin via a valine-citrulline-PABA linker. In a previous study, this antibody-toxin conjugate was found to be effective against triple negative breast cancer cell lines and xenografts, alone, or in combination with cisplatin (1). In this study, we examined the anti-tumor effect of the antibody toxin conjugate (ADC) against activated matriptase positive mantle cell lymphoma cell lines (JeKo-1, Maver, Mino, and Z138). This ADC was cytotoxic to these cell lines with IC(50)s between 5 and 14 μg/mL. The ADC also showed a dose dependent anti-tumor effect on the JeKo-1 xenograft in mice without toxicity. Frontiers Media S.A. 2019-04-10 /pmc/articles/PMC6467949/ /pubmed/31024856 http://dx.doi.org/10.3389/fonc.2019.00258 Text en Copyright © 2019 Rather, Lin, Lin, Szekely and Bertino. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Rather, Gulam M. Lin, Siang-Yo Lin, Hongxia Szekely, Zoltan Bertino, Joseph R. A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title | A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title_full | A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title_fullStr | A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title_full_unstemmed | A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title_short | A Novel Antibody-Toxin Conjugate to Treat Mantle Cell Lymphoma |
title_sort | novel antibody-toxin conjugate to treat mantle cell lymphoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467949/ https://www.ncbi.nlm.nih.gov/pubmed/31024856 http://dx.doi.org/10.3389/fonc.2019.00258 |
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