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Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer

Immune checkpoint inhibitors (ICIs) treatment is becoming a new hope for cancer treatment. However, most prostate cancer (PCa) patients do not benefit from it. In order to achieve the accuracy of ICIs treatment in PCa and reduce unnecessary costs for patients, we have analyzed the data from TCGA dat...

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Autores principales: Gao, Ze, Tao, Yiran, Lai, Yiming, Wang, Qiong, Li, Zean, Peng, Shirong, Chen, Junxiu, Cai, Wenli, Li, Kaiwen, Huang, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423880/
https://www.ncbi.nlm.nih.gov/pubmed/32850758
http://dx.doi.org/10.3389/fbioe.2020.00930
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author Gao, Ze
Tao, Yiran
Lai, Yiming
Wang, Qiong
Li, Zean
Peng, Shirong
Chen, Junxiu
Cai, Wenli
Li, Kaiwen
Huang, Hai
author_facet Gao, Ze
Tao, Yiran
Lai, Yiming
Wang, Qiong
Li, Zean
Peng, Shirong
Chen, Junxiu
Cai, Wenli
Li, Kaiwen
Huang, Hai
author_sort Gao, Ze
collection PubMed
description Immune checkpoint inhibitors (ICIs) treatment is becoming a new hope for cancer treatment. However, most prostate cancer (PCa) patients do not benefit from it. In order to achieve the accuracy of ICIs treatment in PCa and reduce unnecessary costs for patients, we have analyzed the data from TCGA database to find a indicator that can assist the choice of treatment. By analyzing the data of PCa patients with TMB analysis and immune infiltration analysis, we found the expression of immune cells in different immune infiltration groups. Commonly used markers of ICIs, expressed on CD8(+) T cell, were highly expressed in the high immune group. Then we used the forimmune cytolytic activity (CYT) to determine its relationship with the target of ICIs treatment. Through the analysis of CYT score and the ligands of immune checkpoints, we found that there was a significant correlation between them. With the increase of CYT score, the expression of CD80/86, PD-L1/L2, TNFSF14, and LGALS9 also increased gradually. Similarly, CD8(+) T cells were significantly increased in the CYT high group compared with the CYT low group in PRAD. The present research provides novel insights into the immune microenvironment of PRAD and potential immunotherapies. The proposed CYT score is a clinically promising indicator that can serve as a marker to assist anti-PD-L1 or other ICIs treatment. At the same time, it also provides a basis for the selection of other immune checkpoint drugs.
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spelling pubmed-74238802020-08-25 Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer Gao, Ze Tao, Yiran Lai, Yiming Wang, Qiong Li, Zean Peng, Shirong Chen, Junxiu Cai, Wenli Li, Kaiwen Huang, Hai Front Bioeng Biotechnol Bioengineering and Biotechnology Immune checkpoint inhibitors (ICIs) treatment is becoming a new hope for cancer treatment. However, most prostate cancer (PCa) patients do not benefit from it. In order to achieve the accuracy of ICIs treatment in PCa and reduce unnecessary costs for patients, we have analyzed the data from TCGA database to find a indicator that can assist the choice of treatment. By analyzing the data of PCa patients with TMB analysis and immune infiltration analysis, we found the expression of immune cells in different immune infiltration groups. Commonly used markers of ICIs, expressed on CD8(+) T cell, were highly expressed in the high immune group. Then we used the forimmune cytolytic activity (CYT) to determine its relationship with the target of ICIs treatment. Through the analysis of CYT score and the ligands of immune checkpoints, we found that there was a significant correlation between them. With the increase of CYT score, the expression of CD80/86, PD-L1/L2, TNFSF14, and LGALS9 also increased gradually. Similarly, CD8(+) T cells were significantly increased in the CYT high group compared with the CYT low group in PRAD. The present research provides novel insights into the immune microenvironment of PRAD and potential immunotherapies. The proposed CYT score is a clinically promising indicator that can serve as a marker to assist anti-PD-L1 or other ICIs treatment. At the same time, it also provides a basis for the selection of other immune checkpoint drugs. Frontiers Media S.A. 2020-08-06 /pmc/articles/PMC7423880/ /pubmed/32850758 http://dx.doi.org/10.3389/fbioe.2020.00930 Text en Copyright © 2020 Gao, Tao, Lai, Wang, Li, Peng, Chen, Cai, Li and Huang. 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 Bioengineering and Biotechnology
Gao, Ze
Tao, Yiran
Lai, Yiming
Wang, Qiong
Li, Zean
Peng, Shirong
Chen, Junxiu
Cai, Wenli
Li, Kaiwen
Huang, Hai
Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title_full Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title_fullStr Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title_full_unstemmed Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title_short Immune Cytolytic Activity as an Indicator of Immune Checkpoint Inhibitors Treatment for Prostate Cancer
title_sort immune cytolytic activity as an indicator of immune checkpoint inhibitors treatment for prostate cancer
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423880/
https://www.ncbi.nlm.nih.gov/pubmed/32850758
http://dx.doi.org/10.3389/fbioe.2020.00930
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