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Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma

Cathepsin A (CTSA) is a lysosomal protease that regulates galactoside metabolism. The previous study has shown CTSA is abnormally expressed in various types of cancer. However, rarely the previous study has addressed the role of CTSA in hepatocellular carcinoma (HCC) and its prognostic value. To stu...

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Autores principales: Wang, Huaxiang, Xu, Fengfeng, Yang, Fang, Lv, Lizhi, Jiang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285409/
https://www.ncbi.nlm.nih.gov/pubmed/34272452
http://dx.doi.org/10.1038/s41598-021-93998-9
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author Wang, Huaxiang
Xu, Fengfeng
Yang, Fang
Lv, Lizhi
Jiang, Yi
author_facet Wang, Huaxiang
Xu, Fengfeng
Yang, Fang
Lv, Lizhi
Jiang, Yi
author_sort Wang, Huaxiang
collection PubMed
description Cathepsin A (CTSA) is a lysosomal protease that regulates galactoside metabolism. The previous study has shown CTSA is abnormally expressed in various types of cancer. However, rarely the previous study has addressed the role of CTSA in hepatocellular carcinoma (HCC) and its prognostic value. To study the clinical value and potential function of CTSA in HCC, datasets from the Cancer Genome Atlas (TCGA) database and a 136 HCC patient cohort were analyzed. CTSA expression was found to be significantly higher in HCC patients compared with normal liver tissues, which was supported by immunohistochemistry (IHC) validation. Both gene ontology (GO) and The Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses demonstrated that CTSA co-expressed genes were involved in ATP hydrolysis coupled proton transport, carbohydrate metabolic process, lysosome organization, oxidative phosphorylation, other glycan degradation, etc. Survival analysis showed a significant reduction both in overall survival (OS) and recurrence-free survival (RFS) of patients with high CTSA expression from both the TCGA HCC cohort and 136 patients with the HCC cohort. Furthermore, CTSA overexpression has diagnostic value in distinguishing between HCC and normal liver tissue [Area under curve (AUC) = 0.864]. Moreover, Gene set enrichment analysis (GSEA) showed that CTSA expression correlated with the oxidative phosphorylation, proteasome, and lysosome, etc. in HCC tissues. These findings demonstrate that CTSA may as a potential diagnostic and prognostic biomarker in HCC.
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spelling pubmed-82854092021-07-19 Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma Wang, Huaxiang Xu, Fengfeng Yang, Fang Lv, Lizhi Jiang, Yi Sci Rep Article Cathepsin A (CTSA) is a lysosomal protease that regulates galactoside metabolism. The previous study has shown CTSA is abnormally expressed in various types of cancer. However, rarely the previous study has addressed the role of CTSA in hepatocellular carcinoma (HCC) and its prognostic value. To study the clinical value and potential function of CTSA in HCC, datasets from the Cancer Genome Atlas (TCGA) database and a 136 HCC patient cohort were analyzed. CTSA expression was found to be significantly higher in HCC patients compared with normal liver tissues, which was supported by immunohistochemistry (IHC) validation. Both gene ontology (GO) and The Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses demonstrated that CTSA co-expressed genes were involved in ATP hydrolysis coupled proton transport, carbohydrate metabolic process, lysosome organization, oxidative phosphorylation, other glycan degradation, etc. Survival analysis showed a significant reduction both in overall survival (OS) and recurrence-free survival (RFS) of patients with high CTSA expression from both the TCGA HCC cohort and 136 patients with the HCC cohort. Furthermore, CTSA overexpression has diagnostic value in distinguishing between HCC and normal liver tissue [Area under curve (AUC) = 0.864]. Moreover, Gene set enrichment analysis (GSEA) showed that CTSA expression correlated with the oxidative phosphorylation, proteasome, and lysosome, etc. in HCC tissues. These findings demonstrate that CTSA may as a potential diagnostic and prognostic biomarker in HCC. Nature Publishing Group UK 2021-07-16 /pmc/articles/PMC8285409/ /pubmed/34272452 http://dx.doi.org/10.1038/s41598-021-93998-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Huaxiang
Xu, Fengfeng
Yang, Fang
Lv, Lizhi
Jiang, Yi
Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title_full Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title_fullStr Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title_full_unstemmed Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title_short Prognostic significance and oncogene function of cathepsin A in hepatocellular carcinoma
title_sort prognostic significance and oncogene function of cathepsin a in hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285409/
https://www.ncbi.nlm.nih.gov/pubmed/34272452
http://dx.doi.org/10.1038/s41598-021-93998-9
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