Cargando…

PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration

PURPOSE: Hepatocellular carcinoma (HCC) has high morbidity and poor prognosis due to the propensity of recurrence and metastasis. Emerging studies have confirmed that proline-rich coiled-coil2A (PRRC2A) plays a crucial role in tumorigenesis and immunoregulation. However, its expression status and bi...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Xin, Zhang, Yize, Wang, Zenghan, Liu, Liwen, Zhang, Guizhen, Li, Jianhao, Ren, Zhigang, Dong, Zihui, Yu, Zujiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646232/
https://www.ncbi.nlm.nih.gov/pubmed/34881207
http://dx.doi.org/10.2147/JHC.S337111
_version_ 1784610480657006592
author Liu, Xin
Zhang, Yize
Wang, Zenghan
Liu, Liwen
Zhang, Guizhen
Li, Jianhao
Ren, Zhigang
Dong, Zihui
Yu, Zujiang
author_facet Liu, Xin
Zhang, Yize
Wang, Zenghan
Liu, Liwen
Zhang, Guizhen
Li, Jianhao
Ren, Zhigang
Dong, Zihui
Yu, Zujiang
author_sort Liu, Xin
collection PubMed
description PURPOSE: Hepatocellular carcinoma (HCC) has high morbidity and poor prognosis due to the propensity of recurrence and metastasis. Emerging studies have confirmed that proline-rich coiled-coil2A (PRRC2A) plays a crucial role in tumorigenesis and immunoregulation. However, its expression status and biological functions in HCC remain poorly documented. METHODS: The presence and prognostic value of PRRC2A were determined by a tissue microarray (TMA) cohort and multiple databases, mainly from The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), Clinical Proteomic Tumor Analysis Consortium (CPTAC). Functional enrichment analysis was applied to identify the mechanisms of PRRC2A in HCC. The biological function of PRRC2A in HCC progression in vitro was determined by CCK-8, colony formation, EdU, transwell migration and invasion assays. Moreover, the Estimation of STromal and Immune cells in Malignant Tumor tissues using Expression data (ESTIMATE), single-sample gene set enrichment analysis (ssGSEA), tumor immune dysfunction and exclusion (TIDE) algorithms, immunophenoscore (IPS) and public available immunotherapy cohorts were performed to classify their associations with tumor-infiltrating immune cells and immunotherapy. RESULTS: PRRC2A was upregulated in HCC at both mRNA and protein levels. High PRRC2A expression was correlated with poor prognosis and could be an independent risk factor. Functional enrichment analysis demonstrated that elevated PRRC2A was significantly correlated with the activation of various oncogenic pathways. Additionally, in vitro experiments confirmed that silencing PRRC2A could suppress the proliferation and metastasis capacities of HCC cells. More importantly, PRRC2A was negatively associated with many anti-tumor immune cells, but positively related to the expression of markers of exhaustive T cells. And HCC patients with high PRRC2A were more likely to be nonresponsive to immunotherapy. CONCLUSION: This study explored the predictive value and biological roles of PRRC2A in HCC progression and indicated that it might be a potential biomarker for HCC patients and a predictor for immunotherapy.
format Online
Article
Text
id pubmed-8646232
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-86462322021-12-07 PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration Liu, Xin Zhang, Yize Wang, Zenghan Liu, Liwen Zhang, Guizhen Li, Jianhao Ren, Zhigang Dong, Zihui Yu, Zujiang J Hepatocell Carcinoma Original Research PURPOSE: Hepatocellular carcinoma (HCC) has high morbidity and poor prognosis due to the propensity of recurrence and metastasis. Emerging studies have confirmed that proline-rich coiled-coil2A (PRRC2A) plays a crucial role in tumorigenesis and immunoregulation. However, its expression status and biological functions in HCC remain poorly documented. METHODS: The presence and prognostic value of PRRC2A were determined by a tissue microarray (TMA) cohort and multiple databases, mainly from The Cancer Genome Atlas (TCGA), Gene Expression Omnibus (GEO), Clinical Proteomic Tumor Analysis Consortium (CPTAC). Functional enrichment analysis was applied to identify the mechanisms of PRRC2A in HCC. The biological function of PRRC2A in HCC progression in vitro was determined by CCK-8, colony formation, EdU, transwell migration and invasion assays. Moreover, the Estimation of STromal and Immune cells in Malignant Tumor tissues using Expression data (ESTIMATE), single-sample gene set enrichment analysis (ssGSEA), tumor immune dysfunction and exclusion (TIDE) algorithms, immunophenoscore (IPS) and public available immunotherapy cohorts were performed to classify their associations with tumor-infiltrating immune cells and immunotherapy. RESULTS: PRRC2A was upregulated in HCC at both mRNA and protein levels. High PRRC2A expression was correlated with poor prognosis and could be an independent risk factor. Functional enrichment analysis demonstrated that elevated PRRC2A was significantly correlated with the activation of various oncogenic pathways. Additionally, in vitro experiments confirmed that silencing PRRC2A could suppress the proliferation and metastasis capacities of HCC cells. More importantly, PRRC2A was negatively associated with many anti-tumor immune cells, but positively related to the expression of markers of exhaustive T cells. And HCC patients with high PRRC2A were more likely to be nonresponsive to immunotherapy. CONCLUSION: This study explored the predictive value and biological roles of PRRC2A in HCC progression and indicated that it might be a potential biomarker for HCC patients and a predictor for immunotherapy. Dove 2021-12-01 /pmc/articles/PMC8646232/ /pubmed/34881207 http://dx.doi.org/10.2147/JHC.S337111 Text en © 2021 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Xin
Zhang, Yize
Wang, Zenghan
Liu, Liwen
Zhang, Guizhen
Li, Jianhao
Ren, Zhigang
Dong, Zihui
Yu, Zujiang
PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title_full PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title_fullStr PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title_full_unstemmed PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title_short PRRC2A Promotes Hepatocellular Carcinoma Progression and Associates with Immune Infiltration
title_sort prrc2a promotes hepatocellular carcinoma progression and associates with immune infiltration
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646232/
https://www.ncbi.nlm.nih.gov/pubmed/34881207
http://dx.doi.org/10.2147/JHC.S337111
work_keys_str_mv AT liuxin prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT zhangyize prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT wangzenghan prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT liuliwen prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT zhangguizhen prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT lijianhao prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT renzhigang prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT dongzihui prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration
AT yuzujiang prrc2apromoteshepatocellularcarcinomaprogressionandassociateswithimmuneinfiltration