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Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma
Glycogen phosphorylase (GP) is an essential enzyme for glycolysis via the glycogen degradation pathway. It consists of three isoforms: PYGB (brain form), PYGL (liver form) and PYGM (muscle form). Although the abnormal expression of GP is associated with a variety of tumors, its relationship with hep...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214699/ https://www.ncbi.nlm.nih.gov/pubmed/35761940 http://dx.doi.org/10.3892/ol.2022.13364 |
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author | Jiang, Lingyu Liu, Shuyan Deng, Tingzhi Yang, Yang Zhang, Yin |
author_facet | Jiang, Lingyu Liu, Shuyan Deng, Tingzhi Yang, Yang Zhang, Yin |
author_sort | Jiang, Lingyu |
collection | PubMed |
description | Glycogen phosphorylase (GP) is an essential enzyme for glycolysis via the glycogen degradation pathway. It consists of three isoforms: PYGB (brain form), PYGL (liver form) and PYGM (muscle form). Although the abnormal expression of GP is associated with a variety of tumors, its relationship with hepatocellular carcinoma (HCC) and whether it can be used as a prognostic marker of HCC remains unclear. In the present study, the expression levels of PYGB, PYGL and PYGM were analyzed. It was found that the expression levels of PYGB in tumor tissues were higher than those in normal tissues, particularly in HCC. The high expression of PYGB (hazard ratios=1.801; 95% confidence interval: 1.266-2.562) could predict the poor prognosis of HCC patients but not PYGL and PYGM. Inhibition of PYGB with GP inhibitor CP91149 significantly suppressed the HCC cell proliferation in the HCC cell model. In addition, combination treatment with sorafenib, a standard treatment for HCC, showed a great inhibition on tumor growth and angiogenesis. These findings suggested that PYGB may be used as a therapeutic and prognostic indicator for HCC. |
format | Online Article Text |
id | pubmed-9214699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-92146992022-06-26 Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma Jiang, Lingyu Liu, Shuyan Deng, Tingzhi Yang, Yang Zhang, Yin Oncol Lett Articles Glycogen phosphorylase (GP) is an essential enzyme for glycolysis via the glycogen degradation pathway. It consists of three isoforms: PYGB (brain form), PYGL (liver form) and PYGM (muscle form). Although the abnormal expression of GP is associated with a variety of tumors, its relationship with hepatocellular carcinoma (HCC) and whether it can be used as a prognostic marker of HCC remains unclear. In the present study, the expression levels of PYGB, PYGL and PYGM were analyzed. It was found that the expression levels of PYGB in tumor tissues were higher than those in normal tissues, particularly in HCC. The high expression of PYGB (hazard ratios=1.801; 95% confidence interval: 1.266-2.562) could predict the poor prognosis of HCC patients but not PYGL and PYGM. Inhibition of PYGB with GP inhibitor CP91149 significantly suppressed the HCC cell proliferation in the HCC cell model. In addition, combination treatment with sorafenib, a standard treatment for HCC, showed a great inhibition on tumor growth and angiogenesis. These findings suggested that PYGB may be used as a therapeutic and prognostic indicator for HCC. D.A. Spandidos 2022-06-07 /pmc/articles/PMC9214699/ /pubmed/35761940 http://dx.doi.org/10.3892/ol.2022.13364 Text en Copyright: © Jiang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Jiang, Lingyu Liu, Shuyan Deng, Tingzhi Yang, Yang Zhang, Yin Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title | Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title_full | Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title_fullStr | Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title_full_unstemmed | Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title_short | Analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
title_sort | analysis of the expression, function and signaling of glycogen phosphorylase isoforms in hepatocellular carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214699/ https://www.ncbi.nlm.nih.gov/pubmed/35761940 http://dx.doi.org/10.3892/ol.2022.13364 |
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