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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
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.
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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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