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Mutant p53 as an Antigen in Cancer Immunotherapy

The p53 tumor suppressor plays a pivotal role in cancer and infectious disease. Many oncology treatments are now calling on immunotherapy approaches, and scores of studies have investigated the role of p53 antibodies in cancer diagnosis and therapy. This review summarizes the current knowledge from...

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Autores principales: Sobhani, Navid, D’Angelo, Alberto, Wang, Xu, Young, Ken H., Generali, Daniele, Li, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312027/
https://www.ncbi.nlm.nih.gov/pubmed/32521648
http://dx.doi.org/10.3390/ijms21114087
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author Sobhani, Navid
D’Angelo, Alberto
Wang, Xu
Young, Ken H.
Generali, Daniele
Li, Yong
author_facet Sobhani, Navid
D’Angelo, Alberto
Wang, Xu
Young, Ken H.
Generali, Daniele
Li, Yong
author_sort Sobhani, Navid
collection PubMed
description The p53 tumor suppressor plays a pivotal role in cancer and infectious disease. Many oncology treatments are now calling on immunotherapy approaches, and scores of studies have investigated the role of p53 antibodies in cancer diagnosis and therapy. This review summarizes the current knowledge from the preliminary evidence that suggests a potential role of p53 as an antigen in the adaptive immune response and as a key monitor of the innate immune system, thereby speculating on the idea that mutant p53 antigens serve as a druggable targets in immunotherapy. Except in a few cases, the vast majority of published work on p53 antibodies in cancer patients use wild-type p53 as the antigen to detect these antibodies and it is unclear whether they can recognize p53 mutants carried by cancer patients at all. We envision that an antibody targeting a specific mutant p53 will be effective therapeutically against a cancer carrying the exact same mutant p53. To corroborate such a possibility, a recent study showed that a T cell receptor-like (TCLR) antibody, initially made for a wild-type antigen, was capable of discriminating between mutant p53 and wild-type p53, specifically killing more cancer cells expressing mutant p53 than wild-type p53 in vitro and inhibiting the tumour growth of mice injected with mutant p53 cancer cells than mice with wild-type p53 cancer cells. Thus, novel antibodies targeting mutant p53, but not the wild-type isoform, should be pursued in preclinical and clinical studies.
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spelling pubmed-73120272020-06-25 Mutant p53 as an Antigen in Cancer Immunotherapy Sobhani, Navid D’Angelo, Alberto Wang, Xu Young, Ken H. Generali, Daniele Li, Yong Int J Mol Sci Review The p53 tumor suppressor plays a pivotal role in cancer and infectious disease. Many oncology treatments are now calling on immunotherapy approaches, and scores of studies have investigated the role of p53 antibodies in cancer diagnosis and therapy. This review summarizes the current knowledge from the preliminary evidence that suggests a potential role of p53 as an antigen in the adaptive immune response and as a key monitor of the innate immune system, thereby speculating on the idea that mutant p53 antigens serve as a druggable targets in immunotherapy. Except in a few cases, the vast majority of published work on p53 antibodies in cancer patients use wild-type p53 as the antigen to detect these antibodies and it is unclear whether they can recognize p53 mutants carried by cancer patients at all. We envision that an antibody targeting a specific mutant p53 will be effective therapeutically against a cancer carrying the exact same mutant p53. To corroborate such a possibility, a recent study showed that a T cell receptor-like (TCLR) antibody, initially made for a wild-type antigen, was capable of discriminating between mutant p53 and wild-type p53, specifically killing more cancer cells expressing mutant p53 than wild-type p53 in vitro and inhibiting the tumour growth of mice injected with mutant p53 cancer cells than mice with wild-type p53 cancer cells. Thus, novel antibodies targeting mutant p53, but not the wild-type isoform, should be pursued in preclinical and clinical studies. MDPI 2020-06-08 /pmc/articles/PMC7312027/ /pubmed/32521648 http://dx.doi.org/10.3390/ijms21114087 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sobhani, Navid
D’Angelo, Alberto
Wang, Xu
Young, Ken H.
Generali, Daniele
Li, Yong
Mutant p53 as an Antigen in Cancer Immunotherapy
title Mutant p53 as an Antigen in Cancer Immunotherapy
title_full Mutant p53 as an Antigen in Cancer Immunotherapy
title_fullStr Mutant p53 as an Antigen in Cancer Immunotherapy
title_full_unstemmed Mutant p53 as an Antigen in Cancer Immunotherapy
title_short Mutant p53 as an Antigen in Cancer Immunotherapy
title_sort mutant p53 as an antigen in cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312027/
https://www.ncbi.nlm.nih.gov/pubmed/32521648
http://dx.doi.org/10.3390/ijms21114087
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