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Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types
Overexpression of the chondroitin sulfate proteoglycan 4 (CSPG4) has been associated with the pathology of multiple types of such as melanoma, breast cancer, squamous cell carcinoma, mesothelioma, neuroblastoma, adult and pediatric sarcomas, and some hematological cancers. CSPG4 has been reported to...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767725/ https://www.ncbi.nlm.nih.gov/pubmed/29375561 http://dx.doi.org/10.3389/fimmu.2017.01911 |
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author | Ilieva, Kristina M. Cheung, Anthony Mele, Silvia Chiaruttini, Giulia Crescioli, Silvia Griffin, Merope Nakamura, Mano Spicer, James F. Tsoka, Sophia Lacy, Katie E. Tutt, Andrew N. J. Karagiannis, Sophia N. |
author_facet | Ilieva, Kristina M. Cheung, Anthony Mele, Silvia Chiaruttini, Giulia Crescioli, Silvia Griffin, Merope Nakamura, Mano Spicer, James F. Tsoka, Sophia Lacy, Katie E. Tutt, Andrew N. J. Karagiannis, Sophia N. |
author_sort | Ilieva, Kristina M. |
collection | PubMed |
description | Overexpression of the chondroitin sulfate proteoglycan 4 (CSPG4) has been associated with the pathology of multiple types of such as melanoma, breast cancer, squamous cell carcinoma, mesothelioma, neuroblastoma, adult and pediatric sarcomas, and some hematological cancers. CSPG4 has been reported to exhibit a role in the growth and survival as well as in the spreading and metastasis of tumor cells. CSPG4 is overexpressed in several malignant diseases, while it is thought to have restricted and low expression in normal tissues. Thus, CSPG4 has become the target of numerous anticancer treatment approaches, including monoclonal antibody-based therapies. This study reviews key potential anti-CSPG4 antibody and immune-based therapies and examines their direct antiproliferative/metastatic and immune activating mechanisms of action. |
format | Online Article Text |
id | pubmed-5767725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57677252018-01-26 Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types Ilieva, Kristina M. Cheung, Anthony Mele, Silvia Chiaruttini, Giulia Crescioli, Silvia Griffin, Merope Nakamura, Mano Spicer, James F. Tsoka, Sophia Lacy, Katie E. Tutt, Andrew N. J. Karagiannis, Sophia N. Front Immunol Immunology Overexpression of the chondroitin sulfate proteoglycan 4 (CSPG4) has been associated with the pathology of multiple types of such as melanoma, breast cancer, squamous cell carcinoma, mesothelioma, neuroblastoma, adult and pediatric sarcomas, and some hematological cancers. CSPG4 has been reported to exhibit a role in the growth and survival as well as in the spreading and metastasis of tumor cells. CSPG4 is overexpressed in several malignant diseases, while it is thought to have restricted and low expression in normal tissues. Thus, CSPG4 has become the target of numerous anticancer treatment approaches, including monoclonal antibody-based therapies. This study reviews key potential anti-CSPG4 antibody and immune-based therapies and examines their direct antiproliferative/metastatic and immune activating mechanisms of action. Frontiers Media S.A. 2018-01-10 /pmc/articles/PMC5767725/ /pubmed/29375561 http://dx.doi.org/10.3389/fimmu.2017.01911 Text en Copyright © 2018 Ilieva, Cheung, Mele, Chiaruttini, Crescioli, Griffin, Nakamura, Spicer, Tsoka, Lacy, Tutt and Karagiannis. http://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) or licensor 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 | Immunology Ilieva, Kristina M. Cheung, Anthony Mele, Silvia Chiaruttini, Giulia Crescioli, Silvia Griffin, Merope Nakamura, Mano Spicer, James F. Tsoka, Sophia Lacy, Katie E. Tutt, Andrew N. J. Karagiannis, Sophia N. Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title | Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title_full | Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title_fullStr | Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title_full_unstemmed | Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title_short | Chondroitin Sulfate Proteoglycan 4 and Its Potential As an Antibody Immunotherapy Target across Different Tumor Types |
title_sort | chondroitin sulfate proteoglycan 4 and its potential as an antibody immunotherapy target across different tumor types |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767725/ https://www.ncbi.nlm.nih.gov/pubmed/29375561 http://dx.doi.org/10.3389/fimmu.2017.01911 |
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