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Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma
PURPOSE: Ribosomal protein metallopanstimulin-1 (MPS-1) is implicated in tumorigenesis. However, to date, the underlying role of MPS-1 in the generation, progression and prognosis of hepatocellular carcinoma (HCC) remains unknown. This study aims to investigate the expression of MPS-1 in HCC and its...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647167/ https://www.ncbi.nlm.nih.gov/pubmed/34880653 http://dx.doi.org/10.2147/IJGM.S334378 |
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author | Jiang, He Yuan, Feifei Zhao, Zhiying Xue, Tongchun Ge, Ningling Ren, Zhenggang Zhang, Lan |
author_facet | Jiang, He Yuan, Feifei Zhao, Zhiying Xue, Tongchun Ge, Ningling Ren, Zhenggang Zhang, Lan |
author_sort | Jiang, He |
collection | PubMed |
description | PURPOSE: Ribosomal protein metallopanstimulin-1 (MPS-1) is implicated in tumorigenesis. However, to date, the underlying role of MPS-1 in the generation, progression and prognosis of hepatocellular carcinoma (HCC) remains unknown. This study aims to investigate the expression of MPS-1 in HCC and its significance for the prognosis of HCC. METHODS: The Oncomine and GEPIA databases were used to analyze the expression pattern of MPS-1 in HCC. Immunohistochemical staining was performed on tissue microarrays containing 169 HCC tissue samples to examine the expression of MPS-1. In addition, univariate and multivariate Cox regression analyses and Kaplan–Meier analysis were used to verify the correlation between clinicopathological factors in HCC patients and its clinical prognostic significance. RESULTS: MPS-1 was more highly expressed in HCC than in normal tissues, and MPS-1 expression was correlated with serum AFP levels (P = 0.003), liver cirrhosis (P = 0.024), tumor embolus (P = 0.009) and tumor recurrence (P < 0.003). MPS-1 was an independent prognostic factor for the overall survival of HCC (HR, 1.92; 95% CI, 1.01–3.68), and a higher expression of MPS-1 predicted poorer survival. Furthermore, high expression of MPS-1 indicated a poor prognosis in patients with AFP positivity, cirrhosis or HBsAg positivity. CONCLUSION: These findings demonstrate that MPS-1 is highly expressed in HCC and serves as an independent prognostic marker, highlighting the potential role of MPS-1 as a novel biomarker and therapeutic target for HCC. |
format | Online Article Text |
id | pubmed-8647167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-86471672021-12-07 Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma Jiang, He Yuan, Feifei Zhao, Zhiying Xue, Tongchun Ge, Ningling Ren, Zhenggang Zhang, Lan Int J Gen Med Original Research PURPOSE: Ribosomal protein metallopanstimulin-1 (MPS-1) is implicated in tumorigenesis. However, to date, the underlying role of MPS-1 in the generation, progression and prognosis of hepatocellular carcinoma (HCC) remains unknown. This study aims to investigate the expression of MPS-1 in HCC and its significance for the prognosis of HCC. METHODS: The Oncomine and GEPIA databases were used to analyze the expression pattern of MPS-1 in HCC. Immunohistochemical staining was performed on tissue microarrays containing 169 HCC tissue samples to examine the expression of MPS-1. In addition, univariate and multivariate Cox regression analyses and Kaplan–Meier analysis were used to verify the correlation between clinicopathological factors in HCC patients and its clinical prognostic significance. RESULTS: MPS-1 was more highly expressed in HCC than in normal tissues, and MPS-1 expression was correlated with serum AFP levels (P = 0.003), liver cirrhosis (P = 0.024), tumor embolus (P = 0.009) and tumor recurrence (P < 0.003). MPS-1 was an independent prognostic factor for the overall survival of HCC (HR, 1.92; 95% CI, 1.01–3.68), and a higher expression of MPS-1 predicted poorer survival. Furthermore, high expression of MPS-1 indicated a poor prognosis in patients with AFP positivity, cirrhosis or HBsAg positivity. CONCLUSION: These findings demonstrate that MPS-1 is highly expressed in HCC and serves as an independent prognostic marker, highlighting the potential role of MPS-1 as a novel biomarker and therapeutic target for HCC. Dove 2021-12-01 /pmc/articles/PMC8647167/ /pubmed/34880653 http://dx.doi.org/10.2147/IJGM.S334378 Text en © 2021 Jiang 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 Jiang, He Yuan, Feifei Zhao, Zhiying Xue, Tongchun Ge, Ningling Ren, Zhenggang Zhang, Lan Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title | Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title_full | Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title_fullStr | Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title_full_unstemmed | Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title_short | Expression and Clinical Significance of MPS-1 in Hepatocellular Carcinoma |
title_sort | expression and clinical significance of mps-1 in hepatocellular carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647167/ https://www.ncbi.nlm.nih.gov/pubmed/34880653 http://dx.doi.org/10.2147/IJGM.S334378 |
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