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Antitumor activity of an anti‐CD98 antibody
CD98 is expressed on several tissue types and specifically upregulated on fast‐cycling cells undergoing clonal expansion. Various solid (e.g., nonsmall cell lung carcinoma) as well as hematological malignancies (e.g., acute myeloid leukemia) overexpress CD98. We have identified a CD98‐specific mouse...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680144/ https://www.ncbi.nlm.nih.gov/pubmed/25556716 http://dx.doi.org/10.1002/ijc.29415 |
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author | Hayes, Gregory M. Chinn, Lawrence Cantor, Joseph M. Cairns, Belinda Levashova, Zoia Tran, Hoang Velilla, Timothy Duey, Dana Lippincott, John Zachwieja, Joseph Ginsberg, Mark H. H. van der Horst, Edward |
author_facet | Hayes, Gregory M. Chinn, Lawrence Cantor, Joseph M. Cairns, Belinda Levashova, Zoia Tran, Hoang Velilla, Timothy Duey, Dana Lippincott, John Zachwieja, Joseph Ginsberg, Mark H. H. van der Horst, Edward |
author_sort | Hayes, Gregory M. |
collection | PubMed |
description | CD98 is expressed on several tissue types and specifically upregulated on fast‐cycling cells undergoing clonal expansion. Various solid (e.g., nonsmall cell lung carcinoma) as well as hematological malignancies (e.g., acute myeloid leukemia) overexpress CD98. We have identified a CD98‐specific mouse monoclonal antibody that exhibits potent preclinical antitumor activity against established lymphoma tumor xenografts. Additionally, the humanized antibody designated IGN523 demonstrated robust tumor growth inhibition in leukemic cell‐line derived xenograft models and was as efficacious as standard of care carboplatin in patient‐derived nonsmall lung cancer xenografts. In vitro studies revealed that IGN523 elicited strong ADCC activity, induced lysosomal membrane permeabilization and inhibited essential amino acid transport function, ultimately resulting in caspase‐3 and ‐7‐mediated apoptosis of tumor cells. IGN523 is currently being evaluated in a Phase I clinical trial for acute myeloid leukemia (NCT02040506). Furthermore, preclinical data support the therapeutic potential of IGN523 in solid tumors. |
format | Online Article Text |
id | pubmed-6680144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66801442019-08-09 Antitumor activity of an anti‐CD98 antibody Hayes, Gregory M. Chinn, Lawrence Cantor, Joseph M. Cairns, Belinda Levashova, Zoia Tran, Hoang Velilla, Timothy Duey, Dana Lippincott, John Zachwieja, Joseph Ginsberg, Mark H. H. van der Horst, Edward Int J Cancer Cancer Therapy CD98 is expressed on several tissue types and specifically upregulated on fast‐cycling cells undergoing clonal expansion. Various solid (e.g., nonsmall cell lung carcinoma) as well as hematological malignancies (e.g., acute myeloid leukemia) overexpress CD98. We have identified a CD98‐specific mouse monoclonal antibody that exhibits potent preclinical antitumor activity against established lymphoma tumor xenografts. Additionally, the humanized antibody designated IGN523 demonstrated robust tumor growth inhibition in leukemic cell‐line derived xenograft models and was as efficacious as standard of care carboplatin in patient‐derived nonsmall lung cancer xenografts. In vitro studies revealed that IGN523 elicited strong ADCC activity, induced lysosomal membrane permeabilization and inhibited essential amino acid transport function, ultimately resulting in caspase‐3 and ‐7‐mediated apoptosis of tumor cells. IGN523 is currently being evaluated in a Phase I clinical trial for acute myeloid leukemia (NCT02040506). Furthermore, preclinical data support the therapeutic potential of IGN523 in solid tumors. John Wiley and Sons Inc. 2015-01-14 2015-08-01 /pmc/articles/PMC6680144/ /pubmed/25556716 http://dx.doi.org/10.1002/ijc.29415 Text en © 2014 The Authors. Published by Wiley Periodicals, Inc. on behalf of UICC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Cancer Therapy Hayes, Gregory M. Chinn, Lawrence Cantor, Joseph M. Cairns, Belinda Levashova, Zoia Tran, Hoang Velilla, Timothy Duey, Dana Lippincott, John Zachwieja, Joseph Ginsberg, Mark H. H. van der Horst, Edward Antitumor activity of an anti‐CD98 antibody |
title | Antitumor activity of an anti‐CD98 antibody |
title_full | Antitumor activity of an anti‐CD98 antibody |
title_fullStr | Antitumor activity of an anti‐CD98 antibody |
title_full_unstemmed | Antitumor activity of an anti‐CD98 antibody |
title_short | Antitumor activity of an anti‐CD98 antibody |
title_sort | antitumor activity of an anti‐cd98 antibody |
topic | Cancer Therapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680144/ https://www.ncbi.nlm.nih.gov/pubmed/25556716 http://dx.doi.org/10.1002/ijc.29415 |
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