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IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma
BACKGROUND: Epigenetic alterations of tumor-associated genes contribute to the pathogenesis of virtually all cancer types. We evaluated the methylation status of the interleukin-10 (IL-10) gene promoter and assessed its association with IL-10 mRNA expression and clinical prognosis in hepatocellular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797925/ https://www.ncbi.nlm.nih.gov/pubmed/35116889 http://dx.doi.org/10.21037/tcr.2019.07.33 |
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author | Zhang, Xianjing Lu, Mingzhu Xu, Yun He, Guangzhao Liu, Qian Zhu, Jing Zhang, Changsong Zhang, Xiaoli |
author_facet | Zhang, Xianjing Lu, Mingzhu Xu, Yun He, Guangzhao Liu, Qian Zhu, Jing Zhang, Changsong Zhang, Xiaoli |
author_sort | Zhang, Xianjing |
collection | PubMed |
description | BACKGROUND: Epigenetic alterations of tumor-associated genes contribute to the pathogenesis of virtually all cancer types. We evaluated the methylation status of the interleukin-10 (IL-10) gene promoter and assessed its association with IL-10 mRNA expression and clinical prognosis in hepatocellular carcinoma (HCC) patients. METHODS: Methylation-specific polymerase chain reaction (MSP) and real-time polymerase chain reaction (PCR) were used to define the methylation index (MI) of the IL-10 gene and quantify IL-10 mRNA expression in 120 HCC samples and paired non-tumor tissues. RESULTS: Mean MI was 0.47 in HCC specimens and 0.59 in non-tumor controls, and was associated with metastasis classification and serum α-fetoprotein (AFP) levels. IL-10 mRNA levels [mean –∆∆Ct of 1.678 in HCC cases with hypomethylation (∆MI ≤0) and –0.18 in HCC cases with hypermethylation (∆MI >0)] also correlated with metastasis classification and serum AFP. An association was detected between IL-10 mRNA and its gene’s MI in HCC. Also, an association was found between IL-10 hypomethylation, but not IL-10 mRNA expression and reduced postoperative HCC survival. CONCLUSIONS: These results indicate that IL-10 promoter hypomethylation is associated with increased IL-10 mRNA levels and indicative of poor survival in HCC. |
format | Online Article Text |
id | pubmed-8797925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87979252022-02-02 IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma Zhang, Xianjing Lu, Mingzhu Xu, Yun He, Guangzhao Liu, Qian Zhu, Jing Zhang, Changsong Zhang, Xiaoli Transl Cancer Res Original Article BACKGROUND: Epigenetic alterations of tumor-associated genes contribute to the pathogenesis of virtually all cancer types. We evaluated the methylation status of the interleukin-10 (IL-10) gene promoter and assessed its association with IL-10 mRNA expression and clinical prognosis in hepatocellular carcinoma (HCC) patients. METHODS: Methylation-specific polymerase chain reaction (MSP) and real-time polymerase chain reaction (PCR) were used to define the methylation index (MI) of the IL-10 gene and quantify IL-10 mRNA expression in 120 HCC samples and paired non-tumor tissues. RESULTS: Mean MI was 0.47 in HCC specimens and 0.59 in non-tumor controls, and was associated with metastasis classification and serum α-fetoprotein (AFP) levels. IL-10 mRNA levels [mean –∆∆Ct of 1.678 in HCC cases with hypomethylation (∆MI ≤0) and –0.18 in HCC cases with hypermethylation (∆MI >0)] also correlated with metastasis classification and serum AFP. An association was detected between IL-10 mRNA and its gene’s MI in HCC. Also, an association was found between IL-10 hypomethylation, but not IL-10 mRNA expression and reduced postoperative HCC survival. CONCLUSIONS: These results indicate that IL-10 promoter hypomethylation is associated with increased IL-10 mRNA levels and indicative of poor survival in HCC. AME Publishing Company 2019-08 /pmc/articles/PMC8797925/ /pubmed/35116889 http://dx.doi.org/10.21037/tcr.2019.07.33 Text en 2019 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 Zhang, Xianjing Lu, Mingzhu Xu, Yun He, Guangzhao Liu, Qian Zhu, Jing Zhang, Changsong Zhang, Xiaoli IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title | IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title_full | IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title_fullStr | IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title_full_unstemmed | IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title_short | IL-10 promoter hypomethylation is associated with increased IL-10 expression and poor survival in hepatocellular carcinoma |
title_sort | il-10 promoter hypomethylation is associated with increased il-10 expression and poor survival in hepatocellular carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797925/ https://www.ncbi.nlm.nih.gov/pubmed/35116889 http://dx.doi.org/10.21037/tcr.2019.07.33 |
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