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Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma
BACKGROUND: This study aimed to investigate the effect of matrix metalloproteinase-9 (MMP-9) copy number variations (CNVs) on hepatocellular carcinoma (HCC) poor prognosis and recurrence. METHODS: A total of 35 patients were collected between January 2016 and December 2018. The copy number and expre...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797802/ https://www.ncbi.nlm.nih.gov/pubmed/35117415 http://dx.doi.org/10.21037/tcr.2019.11.52 |
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author | Yu, Xi Huang, Jing Wu, Shengdong Huang, Yi Shan, Yuying Lu, Caide |
author_facet | Yu, Xi Huang, Jing Wu, Shengdong Huang, Yi Shan, Yuying Lu, Caide |
author_sort | Yu, Xi |
collection | PubMed |
description | BACKGROUND: This study aimed to investigate the effect of matrix metalloproteinase-9 (MMP-9) copy number variations (CNVs) on hepatocellular carcinoma (HCC) poor prognosis and recurrence. METHODS: A total of 35 patients were collected between January 2016 and December 2018. The copy number and expression level of MMP-9 were measured in 35 HCC tumor tissues and 35 paired adjacent non-tumor tissues using digital polymerase chain reaction (dPCR) and quantitative reverse transcription polymerase chain reaction (RT-qPCR), respectively. RESULTS: Our results showed that MMP-9 expression was significantly upregulated in HCC tumor tissues compared to adjacent non-tumor tissues (5.521±9.545 versus 1.000±0.000, P=0.0047). Interestingly, MMP-9 CNVs only existed in tumor tissues (15/35 versus 0/35, P=0.002). A breakdown analysis by the occurrence of CNVs in tumor tissues had shown that there were significant differences between CNVs group and non-CNVs group in the expression levels of tissue alpha-fetoprotein (AFP) (P=0.015), tumor size (P<0.001), differentiation (P<0.001), microvascular invasion (MVI) (P=0.009), and clinical stage (P<0.001). Receiver operating characteristic (ROC) curves showed that MMP-9 CNVs and expression were significant predictors of HCC [P<0.0001, area under the curve (AUC) =0.76]. CONCLUSIONS: Our results demonstrated that MMP-9 CNVs were a promising diagnostic biomarker for HCC. |
format | Online Article Text |
id | pubmed-8797802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87978022022-02-02 Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma Yu, Xi Huang, Jing Wu, Shengdong Huang, Yi Shan, Yuying Lu, Caide Transl Cancer Res Original Article BACKGROUND: This study aimed to investigate the effect of matrix metalloproteinase-9 (MMP-9) copy number variations (CNVs) on hepatocellular carcinoma (HCC) poor prognosis and recurrence. METHODS: A total of 35 patients were collected between January 2016 and December 2018. The copy number and expression level of MMP-9 were measured in 35 HCC tumor tissues and 35 paired adjacent non-tumor tissues using digital polymerase chain reaction (dPCR) and quantitative reverse transcription polymerase chain reaction (RT-qPCR), respectively. RESULTS: Our results showed that MMP-9 expression was significantly upregulated in HCC tumor tissues compared to adjacent non-tumor tissues (5.521±9.545 versus 1.000±0.000, P=0.0047). Interestingly, MMP-9 CNVs only existed in tumor tissues (15/35 versus 0/35, P=0.002). A breakdown analysis by the occurrence of CNVs in tumor tissues had shown that there were significant differences between CNVs group and non-CNVs group in the expression levels of tissue alpha-fetoprotein (AFP) (P=0.015), tumor size (P<0.001), differentiation (P<0.001), microvascular invasion (MVI) (P=0.009), and clinical stage (P<0.001). Receiver operating characteristic (ROC) curves showed that MMP-9 CNVs and expression were significant predictors of HCC [P<0.0001, area under the curve (AUC) =0.76]. CONCLUSIONS: Our results demonstrated that MMP-9 CNVs were a promising diagnostic biomarker for HCC. AME Publishing Company 2020-02 /pmc/articles/PMC8797802/ /pubmed/35117415 http://dx.doi.org/10.21037/tcr.2019.11.52 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Yu, Xi Huang, Jing Wu, Shengdong Huang, Yi Shan, Yuying Lu, Caide Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title | Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title_full | Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title_fullStr | Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title_full_unstemmed | Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title_short | Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma |
title_sort | copy number variations of mmp-9 are prognostic biomarkers for hepatocellular carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797802/ https://www.ncbi.nlm.nih.gov/pubmed/35117415 http://dx.doi.org/10.21037/tcr.2019.11.52 |
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