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Potential Therapeutic Targets of B7 Family in Colorectal Cancer

Programmed cell death protein 1 (PD-1)/programmed death ligand 1 (PD-L1) pathway blockade has impressively benefited cancer patients with a wide spectrum of tumors. However, its efficacy in colorectal cancer (CRC) is modest, and only a small subset of patients benefits from approved checkpoint inhib...

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Autores principales: Wang, Changgang, Feng, Haoran, Cheng, Xi, Liu, Kun, Cai, Dongli, Zhao, Ren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232583/
https://www.ncbi.nlm.nih.gov/pubmed/32477326
http://dx.doi.org/10.3389/fimmu.2020.00681
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author Wang, Changgang
Feng, Haoran
Cheng, Xi
Liu, Kun
Cai, Dongli
Zhao, Ren
author_facet Wang, Changgang
Feng, Haoran
Cheng, Xi
Liu, Kun
Cai, Dongli
Zhao, Ren
author_sort Wang, Changgang
collection PubMed
description Programmed cell death protein 1 (PD-1)/programmed death ligand 1 (PD-L1) pathway blockade has impressively benefited cancer patients with a wide spectrum of tumors. However, its efficacy in colorectal cancer (CRC) is modest, and only a small subset of patients benefits from approved checkpoint inhibitors. Newer checkpoints that target additional immunomodulatory pathways are becoming necessary to activate durable antitumor immune responses in patients with CRC. In this review, we evaluated the mRNA expression of all 10 reported B7 family members in human CRC by retrieving and analyzing the TCGA database and reviewed the current understanding of the top three B7 family checkpoint molecules (B7-H3, VISTA, and HHLA2) with the highest mRNA expression, introducing them as putative therapeutic targets in CRC.
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spelling pubmed-72325832020-05-29 Potential Therapeutic Targets of B7 Family in Colorectal Cancer Wang, Changgang Feng, Haoran Cheng, Xi Liu, Kun Cai, Dongli Zhao, Ren Front Immunol Immunology Programmed cell death protein 1 (PD-1)/programmed death ligand 1 (PD-L1) pathway blockade has impressively benefited cancer patients with a wide spectrum of tumors. However, its efficacy in colorectal cancer (CRC) is modest, and only a small subset of patients benefits from approved checkpoint inhibitors. Newer checkpoints that target additional immunomodulatory pathways are becoming necessary to activate durable antitumor immune responses in patients with CRC. In this review, we evaluated the mRNA expression of all 10 reported B7 family members in human CRC by retrieving and analyzing the TCGA database and reviewed the current understanding of the top three B7 family checkpoint molecules (B7-H3, VISTA, and HHLA2) with the highest mRNA expression, introducing them as putative therapeutic targets in CRC. Frontiers Media S.A. 2020-05-05 /pmc/articles/PMC7232583/ /pubmed/32477326 http://dx.doi.org/10.3389/fimmu.2020.00681 Text en Copyright © 2020 Wang, Feng, Cheng, Liu, Cai and Zhao. 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) 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 Immunology
Wang, Changgang
Feng, Haoran
Cheng, Xi
Liu, Kun
Cai, Dongli
Zhao, Ren
Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title_full Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title_fullStr Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title_full_unstemmed Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title_short Potential Therapeutic Targets of B7 Family in Colorectal Cancer
title_sort potential therapeutic targets of b7 family in colorectal cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232583/
https://www.ncbi.nlm.nih.gov/pubmed/32477326
http://dx.doi.org/10.3389/fimmu.2020.00681
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