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Mesothelin as a biomarker for targeted therapy
CAR-T cell therapy targeting CD19 has achieved remarkable success in the treatment of B cell malignancies, while various solid malignancies are still refractory for lack of suitable target. In recent years, a large number of studies have sought to find suitable targets with low “on target, off tumor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708176/ https://www.ncbi.nlm.nih.gov/pubmed/31463062 http://dx.doi.org/10.1186/s40364-019-0169-8 |
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author | Lv, Jiang Li, Peng |
author_facet | Lv, Jiang Li, Peng |
author_sort | Lv, Jiang |
collection | PubMed |
description | CAR-T cell therapy targeting CD19 has achieved remarkable success in the treatment of B cell malignancies, while various solid malignancies are still refractory for lack of suitable target. In recent years, a large number of studies have sought to find suitable targets with low “on target, off tumor” concern for the treatment of solid tumors. Mesothelin (MSLN), a tumor-associated antigen broadly overexpressed on various malignant tumor cells, while its expression is generally limited to normal mesothelial cells, is an attractive candidate for targeted therapy. Strategies targeting MSLN, including antibody-based drugs, vaccines and CAR-T therapies, have been assessed in a large number of preclinical investigations and clinical trials. In particular, the development of CAR-T therapy has shown great promise as a treatment for various types of cancers. The safety, efficacy, doses, and pharmacokinetics of relevant strategies have been evaluated in many clinical trials. This review is intended to provide a brief overview of the characteristics of mesothelin and the development of strategies targeting MSLN for solid tumors. Further, we discussed the challenges and proposed potential strategies to improve the efficacy of MSLN targeted immunotherapy. |
format | Online Article Text |
id | pubmed-6708176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67081762019-08-28 Mesothelin as a biomarker for targeted therapy Lv, Jiang Li, Peng Biomark Res Review CAR-T cell therapy targeting CD19 has achieved remarkable success in the treatment of B cell malignancies, while various solid malignancies are still refractory for lack of suitable target. In recent years, a large number of studies have sought to find suitable targets with low “on target, off tumor” concern for the treatment of solid tumors. Mesothelin (MSLN), a tumor-associated antigen broadly overexpressed on various malignant tumor cells, while its expression is generally limited to normal mesothelial cells, is an attractive candidate for targeted therapy. Strategies targeting MSLN, including antibody-based drugs, vaccines and CAR-T therapies, have been assessed in a large number of preclinical investigations and clinical trials. In particular, the development of CAR-T therapy has shown great promise as a treatment for various types of cancers. The safety, efficacy, doses, and pharmacokinetics of relevant strategies have been evaluated in many clinical trials. This review is intended to provide a brief overview of the characteristics of mesothelin and the development of strategies targeting MSLN for solid tumors. Further, we discussed the challenges and proposed potential strategies to improve the efficacy of MSLN targeted immunotherapy. BioMed Central 2019-08-23 /pmc/articles/PMC6708176/ /pubmed/31463062 http://dx.doi.org/10.1186/s40364-019-0169-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Lv, Jiang Li, Peng Mesothelin as a biomarker for targeted therapy |
title | Mesothelin as a biomarker for targeted therapy |
title_full | Mesothelin as a biomarker for targeted therapy |
title_fullStr | Mesothelin as a biomarker for targeted therapy |
title_full_unstemmed | Mesothelin as a biomarker for targeted therapy |
title_short | Mesothelin as a biomarker for targeted therapy |
title_sort | mesothelin as a biomarker for targeted therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708176/ https://www.ncbi.nlm.nih.gov/pubmed/31463062 http://dx.doi.org/10.1186/s40364-019-0169-8 |
work_keys_str_mv | AT lvjiang mesothelinasabiomarkerfortargetedtherapy AT lipeng mesothelinasabiomarkerfortargetedtherapy |