β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development

Abstract β-defensin family plays a role in host defense against viral infection, however its role in HCV infection is still unknown. In this study, we demonstrated that β-defensin 1 was significantly reduced in HCV-infected liver specimens. Treatment with interferon and ribavirin upregulated β-defen...

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Autores principales: Yue-Ming Ling, Jin-Yu Chen, Libin Guo, Chen-Yi Wang, Wen-Ting Tan, Qing Wen, Shu-Dong Zhang, Guo-Hong Deng, Yao Lin, Hang Fai Kwok
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/35a3888c4b1b4537837048423ababe71
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spelling oai:doaj.org-article:35a3888c4b1b4537837048423ababe712021-12-02T11:52:30Zβ-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development10.1038/s41598-017-13332-02045-2322https://doaj.org/article/35a3888c4b1b4537837048423ababe712017-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-13332-0https://doaj.org/toc/2045-2322Abstract β-defensin family plays a role in host defense against viral infection, however its role in HCV infection is still unknown. In this study, we demonstrated that β-defensin 1 was significantly reduced in HCV-infected liver specimens. Treatment with interferon and ribavirin upregulated β-defensin-1, but not other β-defensin tested, with the extent and duration of upregulation associated with treatment response. We investigated β-defensin family expression in liver cancer in publicly available datasets and found that among all the β-defensins tested, only β-defensin 1 was significantly downregulated, suggesting β-defensin 1 plays a crucial role in liver cancer development. Further analysis identified E-cadherin as the top positive correlated gene, while hepatocyte growth factor-regulated tyrosine kinase substrate as the top negative correlated gene. Expression of two proteoglycans were also positively correlated with that of β-defensin 1. We have also identified small molecules as potential therapeutic agents to reverse β-defensin 1-associated gene signature. Furthermore, the downregulation of β-defensin 1 and E-cadherin, and upregulation of hepatocyte growth factor-regulated tyrosine kinase substrate, were further confirmed in liver cancer and adjacent normal tissue collected from in-house Chinese liver cancer patients. Together, our results suggest β-defensin 1 plays an important role in protecting HCV progression and liver cancer development.Yue-Ming LingJin-Yu ChenLibin GuoChen-Yi WangWen-Ting TanQing WenShu-Dong ZhangGuo-Hong DengYao LinHang Fai KwokNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yue-Ming Ling
Jin-Yu Chen
Libin Guo
Chen-Yi Wang
Wen-Ting Tan
Qing Wen
Shu-Dong Zhang
Guo-Hong Deng
Yao Lin
Hang Fai Kwok
β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
description Abstract β-defensin family plays a role in host defense against viral infection, however its role in HCV infection is still unknown. In this study, we demonstrated that β-defensin 1 was significantly reduced in HCV-infected liver specimens. Treatment with interferon and ribavirin upregulated β-defensin-1, but not other β-defensin tested, with the extent and duration of upregulation associated with treatment response. We investigated β-defensin family expression in liver cancer in publicly available datasets and found that among all the β-defensins tested, only β-defensin 1 was significantly downregulated, suggesting β-defensin 1 plays a crucial role in liver cancer development. Further analysis identified E-cadherin as the top positive correlated gene, while hepatocyte growth factor-regulated tyrosine kinase substrate as the top negative correlated gene. Expression of two proteoglycans were also positively correlated with that of β-defensin 1. We have also identified small molecules as potential therapeutic agents to reverse β-defensin 1-associated gene signature. Furthermore, the downregulation of β-defensin 1 and E-cadherin, and upregulation of hepatocyte growth factor-regulated tyrosine kinase substrate, were further confirmed in liver cancer and adjacent normal tissue collected from in-house Chinese liver cancer patients. Together, our results suggest β-defensin 1 plays an important role in protecting HCV progression and liver cancer development.
format article
author Yue-Ming Ling
Jin-Yu Chen
Libin Guo
Chen-Yi Wang
Wen-Ting Tan
Qing Wen
Shu-Dong Zhang
Guo-Hong Deng
Yao Lin
Hang Fai Kwok
author_facet Yue-Ming Ling
Jin-Yu Chen
Libin Guo
Chen-Yi Wang
Wen-Ting Tan
Qing Wen
Shu-Dong Zhang
Guo-Hong Deng
Yao Lin
Hang Fai Kwok
author_sort Yue-Ming Ling
title β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
title_short β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
title_full β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
title_fullStr β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
title_full_unstemmed β-defensin 1 expression in HCV infected liver/liver cancer: an important role in protecting HCV progression and liver cancer development
title_sort β-defensin 1 expression in hcv infected liver/liver cancer: an important role in protecting hcv progression and liver cancer development
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/35a3888c4b1b4537837048423ababe71
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