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CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment
Hepatocellular carcinoma (HCC) is a lethal malignancy with a lack of effective treatments particularly for the disease at an advanced stage. Even though immune checkpoint inhibitors (ICIs) have made great progress in the treatment of HCC, durable and ideal clinical benefits still cannot be achieved...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061011/ https://www.ncbi.nlm.nih.gov/pubmed/37006233 http://dx.doi.org/10.3389/fimmu.2023.1052657 |
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author | Han, Rui Li, Jiayin Hony, Jing Xiao, Zhiwei wang, Jinghui Yao, Man Liang, Shufang Lu, Lingeng |
author_facet | Han, Rui Li, Jiayin Hony, Jing Xiao, Zhiwei wang, Jinghui Yao, Man Liang, Shufang Lu, Lingeng |
author_sort | Han, Rui |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is a lethal malignancy with a lack of effective treatments particularly for the disease at an advanced stage. Even though immune checkpoint inhibitors (ICIs) have made great progress in the treatment of HCC, durable and ideal clinical benefits still cannot be achieved in plenty of patients with HCC. Therefore, novel and refined ICI-based combination therapies are still needed to enhance the therapeutic effect. The latest study has reported that the carbonic anhydrase XII inhibitor (CAXIIi), a novel type of anticancer drug, can modify the tumor immunosuppression microenvironment by affecting hypoxic/acidic metabolism and alter the functions of monocytes and macrophages by regulating the expression of C-C motif chemokine ligand 8 (CCL8). These observations shine a light on improving programmed cell death protein 1 (PD-1)/programmed cell death ligand-1 (PD-L1) immunotherapy in combination with CAXIIis. This mini-review aims to ignite enthusiasm to explore the potential application of CAXIIis in combination with immunotherapy for HCC. |
format | Online Article Text |
id | pubmed-10061011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100610112023-03-31 CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment Han, Rui Li, Jiayin Hony, Jing Xiao, Zhiwei wang, Jinghui Yao, Man Liang, Shufang Lu, Lingeng Front Immunol Immunology Hepatocellular carcinoma (HCC) is a lethal malignancy with a lack of effective treatments particularly for the disease at an advanced stage. Even though immune checkpoint inhibitors (ICIs) have made great progress in the treatment of HCC, durable and ideal clinical benefits still cannot be achieved in plenty of patients with HCC. Therefore, novel and refined ICI-based combination therapies are still needed to enhance the therapeutic effect. The latest study has reported that the carbonic anhydrase XII inhibitor (CAXIIi), a novel type of anticancer drug, can modify the tumor immunosuppression microenvironment by affecting hypoxic/acidic metabolism and alter the functions of monocytes and macrophages by regulating the expression of C-C motif chemokine ligand 8 (CCL8). These observations shine a light on improving programmed cell death protein 1 (PD-1)/programmed cell death ligand-1 (PD-L1) immunotherapy in combination with CAXIIis. This mini-review aims to ignite enthusiasm to explore the potential application of CAXIIis in combination with immunotherapy for HCC. Frontiers Media S.A. 2023-03-16 /pmc/articles/PMC10061011/ /pubmed/37006233 http://dx.doi.org/10.3389/fimmu.2023.1052657 Text en Copyright © 2023 Han, Li, Hony, Xiao, wang, Yao, Liang and Lu 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 | Immunology Han, Rui Li, Jiayin Hony, Jing Xiao, Zhiwei wang, Jinghui Yao, Man Liang, Shufang Lu, Lingeng CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title | CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title_full | CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title_fullStr | CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title_full_unstemmed | CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title_short | CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment |
title_sort | caxii inhibitors: potential sensitizers for immune checkpoint inhibitors in hcc treatment |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061011/ https://www.ncbi.nlm.nih.gov/pubmed/37006233 http://dx.doi.org/10.3389/fimmu.2023.1052657 |
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