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Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes

Recent studies demonstrate that immune checkpoint inhibitor (ICI) therapy has achieved success in many types of advanced cancers including advanced hepatocellular carcinoma (HCC). However, ICI therapy is beneficial in only some HCC patients, suggesting that immune-responses are highly variable in HC...

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Autores principales: Cao, Di, Chen, Meng-Ke, Zhang, Qing-Feng, Zhou, Yu-Feng, Zhang, Mei-Yin, Mai, Shi-Juan, Zhang, Yao-Jun, Chen, Min-Shan, Li, Xiao-Xing, Wang, Hui-Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343492/
https://www.ncbi.nlm.nih.gov/pubmed/32544882
http://dx.doi.org/10.18632/aging.103395
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author Cao, Di
Chen, Meng-Ke
Zhang, Qing-Feng
Zhou, Yu-Feng
Zhang, Mei-Yin
Mai, Shi-Juan
Zhang, Yao-Jun
Chen, Min-Shan
Li, Xiao-Xing
Wang, Hui-Yun
author_facet Cao, Di
Chen, Meng-Ke
Zhang, Qing-Feng
Zhou, Yu-Feng
Zhang, Mei-Yin
Mai, Shi-Juan
Zhang, Yao-Jun
Chen, Min-Shan
Li, Xiao-Xing
Wang, Hui-Yun
author_sort Cao, Di
collection PubMed
description Recent studies demonstrate that immune checkpoint inhibitor (ICI) therapy has achieved success in many types of advanced cancers including advanced hepatocellular carcinoma (HCC). However, ICI therapy is beneficial in only some HCC patients, suggesting that immune-responses are highly variable in HCCs. Therefore, understanding the immune status in HCC microenvironment will facilitate ICI immunotherapy and guide patient selection for the therapy. In this study, we first analyzed the expression profile of immune-modulating genes and their relationship with survival of HCC patients using the data downloaded from The Cancer Genome Atlas - Liver Hepatocellular Carcinoma (TCGA-LIHC) database, and found that the higher expressions of CD276 (B7-H3) and CD47 were significantly associated with poor survival. Then we identified 4 immune subtypes of HCCs with different survivals by using the combination expression of B7-H3 (or CD47) and CD8. Patients with B7-H3(low)/CD8(high) or CD47(low)/CD8(high) have the best survival while ones with B7-H3(high)/CD8(low) or CD47(high)/CD8(low) have the worst survival. The 4 immune subtypes were validated in another 72 HCC patients obtained from South China. In conclusion, our findings suggest that HCC patient prognosis is associated with immunophenotypes by T cell infiltration (CD8 expression) and the expression of the adaptive immune resistance gene (B7-H3 or CD47), and this immune classification system will facilitate HCC patient selection for ICI immunotherapy.
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spelling pubmed-73434922020-07-15 Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes Cao, Di Chen, Meng-Ke Zhang, Qing-Feng Zhou, Yu-Feng Zhang, Mei-Yin Mai, Shi-Juan Zhang, Yao-Jun Chen, Min-Shan Li, Xiao-Xing Wang, Hui-Yun Aging (Albany NY) Research Paper Recent studies demonstrate that immune checkpoint inhibitor (ICI) therapy has achieved success in many types of advanced cancers including advanced hepatocellular carcinoma (HCC). However, ICI therapy is beneficial in only some HCC patients, suggesting that immune-responses are highly variable in HCCs. Therefore, understanding the immune status in HCC microenvironment will facilitate ICI immunotherapy and guide patient selection for the therapy. In this study, we first analyzed the expression profile of immune-modulating genes and their relationship with survival of HCC patients using the data downloaded from The Cancer Genome Atlas - Liver Hepatocellular Carcinoma (TCGA-LIHC) database, and found that the higher expressions of CD276 (B7-H3) and CD47 were significantly associated with poor survival. Then we identified 4 immune subtypes of HCCs with different survivals by using the combination expression of B7-H3 (or CD47) and CD8. Patients with B7-H3(low)/CD8(high) or CD47(low)/CD8(high) have the best survival while ones with B7-H3(high)/CD8(low) or CD47(high)/CD8(low) have the worst survival. The 4 immune subtypes were validated in another 72 HCC patients obtained from South China. In conclusion, our findings suggest that HCC patient prognosis is associated with immunophenotypes by T cell infiltration (CD8 expression) and the expression of the adaptive immune resistance gene (B7-H3 or CD47), and this immune classification system will facilitate HCC patient selection for ICI immunotherapy. Impact Journals 2020-06-16 /pmc/articles/PMC7343492/ /pubmed/32544882 http://dx.doi.org/10.18632/aging.103395 Text en Copyright © 2020 Cao et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Cao, Di
Chen, Meng-Ke
Zhang, Qing-Feng
Zhou, Yu-Feng
Zhang, Mei-Yin
Mai, Shi-Juan
Zhang, Yao-Jun
Chen, Min-Shan
Li, Xiao-Xing
Wang, Hui-Yun
Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title_full Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title_fullStr Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title_full_unstemmed Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title_short Identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
title_sort identification of immunological subtypes of hepatocellular carcinoma with expression profiling of immune-modulating genes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343492/
https://www.ncbi.nlm.nih.gov/pubmed/32544882
http://dx.doi.org/10.18632/aging.103395
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