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Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers

The high expression of uPAR has been linked to tumor progression, invasion, and metastasis in several types of cancer. Such overexpression of uPAR makes it a potential target for immunotherapies across common cancers such as breast, colorectal, lung, ovarian cancer, and melanoma. In our study, two h...

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Autores principales: Chu, Xiaojie, Li, Wei, Hines, Margaret G., Lyakhov, Ilya, Mellors, John W., Dimitrov, Dimiter S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593477/
https://www.ncbi.nlm.nih.gov/pubmed/37876962
http://dx.doi.org/10.3389/fonc.2023.1194972
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author Chu, Xiaojie
Li, Wei
Hines, Margaret G.
Lyakhov, Ilya
Mellors, John W.
Dimitrov, Dimiter S.
author_facet Chu, Xiaojie
Li, Wei
Hines, Margaret G.
Lyakhov, Ilya
Mellors, John W.
Dimitrov, Dimiter S.
author_sort Chu, Xiaojie
collection PubMed
description The high expression of uPAR has been linked to tumor progression, invasion, and metastasis in several types of cancer. Such overexpression of uPAR makes it a potential target for immunotherapies across common cancers such as breast, colorectal, lung, ovarian cancer, and melanoma. In our study, two high-affinity and specific human V(H) domain antibody candidates, designed as clones 3 and 115, were isolated from a phage-displayed human V(H) antibody library. Domain-based bispecific T- cell engagers (DbTE) based on these two antibodies exhibited potent killing of uPAR-positive cancer cells. Thus, these two anti-uPAR domain antibodies are promising candidates for treating uPAR positive cancers.
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spelling pubmed-105934772023-10-24 Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers Chu, Xiaojie Li, Wei Hines, Margaret G. Lyakhov, Ilya Mellors, John W. Dimitrov, Dimiter S. Front Oncol Oncology The high expression of uPAR has been linked to tumor progression, invasion, and metastasis in several types of cancer. Such overexpression of uPAR makes it a potential target for immunotherapies across common cancers such as breast, colorectal, lung, ovarian cancer, and melanoma. In our study, two high-affinity and specific human V(H) domain antibody candidates, designed as clones 3 and 115, were isolated from a phage-displayed human V(H) antibody library. Domain-based bispecific T- cell engagers (DbTE) based on these two antibodies exhibited potent killing of uPAR-positive cancer cells. Thus, these two anti-uPAR domain antibodies are promising candidates for treating uPAR positive cancers. Frontiers Media S.A. 2023-10-09 /pmc/articles/PMC10593477/ /pubmed/37876962 http://dx.doi.org/10.3389/fonc.2023.1194972 Text en Copyright © 2023 Chu, Li, Hines, Lyakhov, Mellors and Dimitrov https://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
Chu, Xiaojie
Li, Wei
Hines, Margaret G.
Lyakhov, Ilya
Mellors, John W.
Dimitrov, Dimiter S.
Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title_full Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title_fullStr Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title_full_unstemmed Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title_short Human antibody V(H) domains targeting uPAR as candidate therapeutics for cancers
title_sort human antibody v(h) domains targeting upar as candidate therapeutics for cancers
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593477/
https://www.ncbi.nlm.nih.gov/pubmed/37876962
http://dx.doi.org/10.3389/fonc.2023.1194972
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