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Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study
Background: Aberrant expression of pepsinogen C (PGC) has been observed in human cancers. However, its role in hepatocellular carcinoma (HCC) remains to be established. The goal of this study is to illustrate PGC expression and to evaluate its clinical relevance in HCC. Materials and methods: PGC ex...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497866/ https://www.ncbi.nlm.nih.gov/pubmed/31114341 http://dx.doi.org/10.2147/CMAR.S192241 |
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author | Chen, Hong Zhu, Hai-Rong Yu, Xiang-Nan Shi, Xuan Bilegsaikhan, Enkhnaran Guo, Hong-Ying Huang, Ren-Zheng Liu, Tao-Tao Shen, Xi-Zhong Zhu, Ji-Min |
author_facet | Chen, Hong Zhu, Hai-Rong Yu, Xiang-Nan Shi, Xuan Bilegsaikhan, Enkhnaran Guo, Hong-Ying Huang, Ren-Zheng Liu, Tao-Tao Shen, Xi-Zhong Zhu, Ji-Min |
author_sort | Chen, Hong |
collection | PubMed |
description | Background: Aberrant expression of pepsinogen C (PGC) has been observed in human cancers. However, its role in hepatocellular carcinoma (HCC) remains to be established. The goal of this study is to illustrate PGC expression and to evaluate its clinical relevance in HCC. Materials and methods: PGC expression was examined in 75 pairs of HCC and adjacent non-tumor tissues using tissue microarray. The correlations between its expression and clinical parameters were also analyzed. Results: PGC overexpression was significantly associated with larger tumor size (≥5 cm; P=0.017) and incomplete encapsulation (P<0.0001). Cox regression model demonstrated that PGC expression and tumor size were independent prognostic factors for overall survival (OS) and disease-free survival (DFS) in HCC. The subgroup analysis by Kaplan–Meier uncovered that OS and DFS were much worse in high PGC level group than in low PGC level group with large tumor size subgroup, while no difference of OS was noted between the two groups with low tumor size subgroup. Conclusion: PGC plays a tumorigenesis role in HCC progression, which may lead to a novel insight to the potential biomarker and novel therapeutic strategies for HCC patients. |
format | Online Article Text |
id | pubmed-6497866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-64978662019-05-21 Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study Chen, Hong Zhu, Hai-Rong Yu, Xiang-Nan Shi, Xuan Bilegsaikhan, Enkhnaran Guo, Hong-Ying Huang, Ren-Zheng Liu, Tao-Tao Shen, Xi-Zhong Zhu, Ji-Min Cancer Manag Res Original Research Background: Aberrant expression of pepsinogen C (PGC) has been observed in human cancers. However, its role in hepatocellular carcinoma (HCC) remains to be established. The goal of this study is to illustrate PGC expression and to evaluate its clinical relevance in HCC. Materials and methods: PGC expression was examined in 75 pairs of HCC and adjacent non-tumor tissues using tissue microarray. The correlations between its expression and clinical parameters were also analyzed. Results: PGC overexpression was significantly associated with larger tumor size (≥5 cm; P=0.017) and incomplete encapsulation (P<0.0001). Cox regression model demonstrated that PGC expression and tumor size were independent prognostic factors for overall survival (OS) and disease-free survival (DFS) in HCC. The subgroup analysis by Kaplan–Meier uncovered that OS and DFS were much worse in high PGC level group than in low PGC level group with large tumor size subgroup, while no difference of OS was noted between the two groups with low tumor size subgroup. Conclusion: PGC plays a tumorigenesis role in HCC progression, which may lead to a novel insight to the potential biomarker and novel therapeutic strategies for HCC patients. Dove 2019-04-10 /pmc/articles/PMC6497866/ /pubmed/31114341 http://dx.doi.org/10.2147/CMAR.S192241 Text en © 2019 Chen et al. http://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/). 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 Chen, Hong Zhu, Hai-Rong Yu, Xiang-Nan Shi, Xuan Bilegsaikhan, Enkhnaran Guo, Hong-Ying Huang, Ren-Zheng Liu, Tao-Tao Shen, Xi-Zhong Zhu, Ji-Min Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title | Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title_full | Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title_fullStr | Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title_full_unstemmed | Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title_short | Overexpressed pepsinogen C is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
title_sort | overexpressed pepsinogen c is associated with poor prognosis in human hepatocellular carcinoma: a tissue microarray study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497866/ https://www.ncbi.nlm.nih.gov/pubmed/31114341 http://dx.doi.org/10.2147/CMAR.S192241 |
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