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An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma
BACKGROUND: The tumor microenvironment is largely orchestrated by the immune cells. Considerable evidence has shown their excellent clinicopathological application value in assessment of clinical outcomes and immunotherapy efficacy. Hence, a moderate, individualized prognostic signature based on imm...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285951/ https://www.ncbi.nlm.nih.gov/pubmed/32527991 http://dx.doi.org/10.12659/MSM.921786 |
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author | Wang, Xiaodong Wu, Yuquan Wen, Dongyue Wu, Lin-yong Zhao, Yujia He, Yun Yang, Hong |
author_facet | Wang, Xiaodong Wu, Yuquan Wen, Dongyue Wu, Lin-yong Zhao, Yujia He, Yun Yang, Hong |
author_sort | Wang, Xiaodong |
collection | PubMed |
description | BACKGROUND: The tumor microenvironment is largely orchestrated by the immune cells. Considerable evidence has shown their excellent clinicopathological application value in assessment of clinical outcomes and immunotherapy efficacy. Hence, a moderate, individualized prognostic signature based on immune cells that can estimate prognosis and reflect the immune microenvironment in hepatocellular carcinoma (HCC) patients is greatly needed. MATERIAL/METHODS: Here, we systematically analyzed the expression differences and survival prediction value of tumor infiltrating immune cells by analyzing 638 HCC patients from 3 public cohorts, including 2 microarray datasets and 1 RNA sequencing dataset. CIBERSORT software, a computational algorithm, was used to calculate the relative levels of immune cells. Three immune microenvironment subtypes were defined via ConsensuClusterPlus package. Univariate and multivariate survival analyses were used to develop an individualized immune prognostic index based on immune cell pairs. RESULTS: Notably, HCC patients with higher immune signatures score, utterly appreciable, suffered inferior prognosis (hazard ratio=2.742; 95% confidence interval: 1.887–3.983; P<0.001). Subgroup analysis suggested that the prognostic signature did particularly well in early-stage patients. Furthermore, moderate survival prediction value was also confirmed in another two independent cohorts GSE14520 and GSE76427. CONCLUSIONS: This study provides a systematic view of the immune cells characteristics in HCC and suggests their superior survival monitoring performance. |
format | Online Article Text |
id | pubmed-7285951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72859512020-06-19 An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma Wang, Xiaodong Wu, Yuquan Wen, Dongyue Wu, Lin-yong Zhao, Yujia He, Yun Yang, Hong Med Sci Monit Database Analysis BACKGROUND: The tumor microenvironment is largely orchestrated by the immune cells. Considerable evidence has shown their excellent clinicopathological application value in assessment of clinical outcomes and immunotherapy efficacy. Hence, a moderate, individualized prognostic signature based on immune cells that can estimate prognosis and reflect the immune microenvironment in hepatocellular carcinoma (HCC) patients is greatly needed. MATERIAL/METHODS: Here, we systematically analyzed the expression differences and survival prediction value of tumor infiltrating immune cells by analyzing 638 HCC patients from 3 public cohorts, including 2 microarray datasets and 1 RNA sequencing dataset. CIBERSORT software, a computational algorithm, was used to calculate the relative levels of immune cells. Three immune microenvironment subtypes were defined via ConsensuClusterPlus package. Univariate and multivariate survival analyses were used to develop an individualized immune prognostic index based on immune cell pairs. RESULTS: Notably, HCC patients with higher immune signatures score, utterly appreciable, suffered inferior prognosis (hazard ratio=2.742; 95% confidence interval: 1.887–3.983; P<0.001). Subgroup analysis suggested that the prognostic signature did particularly well in early-stage patients. Furthermore, moderate survival prediction value was also confirmed in another two independent cohorts GSE14520 and GSE76427. CONCLUSIONS: This study provides a systematic view of the immune cells characteristics in HCC and suggests their superior survival monitoring performance. International Scientific Literature, Inc. 2020-05-31 /pmc/articles/PMC7285951/ /pubmed/32527991 http://dx.doi.org/10.12659/MSM.921786 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Database Analysis Wang, Xiaodong Wu, Yuquan Wen, Dongyue Wu, Lin-yong Zhao, Yujia He, Yun Yang, Hong An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title | An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title_full | An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title_fullStr | An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title_full_unstemmed | An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title_short | An Individualized Immune Prognostic Index is a Superior Predictor of Survival of Hepatocellular Carcinoma |
title_sort | individualized immune prognostic index is a superior predictor of survival of hepatocellular carcinoma |
topic | Database Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285951/ https://www.ncbi.nlm.nih.gov/pubmed/32527991 http://dx.doi.org/10.12659/MSM.921786 |
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