Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease

As a result of increased prevalence of obesity worldwide, non-alcoholic fatty liver disease (NAFLD) has become one of the most common causes of chronic liver disease. Although most NAFLD cases remain benign, some progress to end-stage liver diseases such as cirrhosis and hepatocellular carcinoma. Th...

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Autores principales: Yong Jiang, Tao Han, Zhi-Guang Zhang, Man Li, Feng-Xiang Qi, Ying Zhang, Ying-Lan Ji
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Publicado: KeAi Communications Co., Ltd. 2017
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spelling oai:doaj.org-article:a2dc2abff5b64dabb16e2113912d964a2021-12-02T14:11:50ZPotential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease2095-882X10.1016/j.cdtm.2017.06.003https://doaj.org/article/a2dc2abff5b64dabb16e2113912d964a2017-09-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2095882X16301645https://doaj.org/toc/2095-882XAs a result of increased prevalence of obesity worldwide, non-alcoholic fatty liver disease (NAFLD) has become one of the most common causes of chronic liver disease. Although most NAFLD cases remain benign, some progress to end-stage liver diseases such as cirrhosis and hepatocellular carcinoma. Therefore, treatment should be considered for NAFLD patients who are likely to progress to nonalcoholic steatohepatitis (NASH) or fibrosis. Thymosin beta 4 (Tβ4), a G-actin sequestering peptide, regulates actin polymerization in mammalian cells. In addition, studies have reported anti-inflammatory, insulin-sensitizing, and anti-fibrotic effects of Tβ4. However, no research has been done to investigate the effects of Tβ4 on NAFLD. Based on the findings above mentioned, we hypothesize that Tβ4 may represent an effective treatment for NAFLD. Keywords: Thymosin beta 4, Nonalcoholic fatty liver disease, Nonalcoholic steatohepatitis, HypothesisYong JiangTao HanZhi-Guang ZhangMan LiFeng-Xiang QiYing ZhangYing-Lan JiKeAi Communications Co., Ltd.articleMedicine (General)R5-920ENChronic Diseases and Translational Medicine, Vol 3, Iss 3, Pp 165-168 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Yong Jiang
Tao Han
Zhi-Guang Zhang
Man Li
Feng-Xiang Qi
Ying Zhang
Ying-Lan Ji
Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
description As a result of increased prevalence of obesity worldwide, non-alcoholic fatty liver disease (NAFLD) has become one of the most common causes of chronic liver disease. Although most NAFLD cases remain benign, some progress to end-stage liver diseases such as cirrhosis and hepatocellular carcinoma. Therefore, treatment should be considered for NAFLD patients who are likely to progress to nonalcoholic steatohepatitis (NASH) or fibrosis. Thymosin beta 4 (Tβ4), a G-actin sequestering peptide, regulates actin polymerization in mammalian cells. In addition, studies have reported anti-inflammatory, insulin-sensitizing, and anti-fibrotic effects of Tβ4. However, no research has been done to investigate the effects of Tβ4 on NAFLD. Based on the findings above mentioned, we hypothesize that Tβ4 may represent an effective treatment for NAFLD. Keywords: Thymosin beta 4, Nonalcoholic fatty liver disease, Nonalcoholic steatohepatitis, Hypothesis
format article
author Yong Jiang
Tao Han
Zhi-Guang Zhang
Man Li
Feng-Xiang Qi
Ying Zhang
Ying-Lan Ji
author_facet Yong Jiang
Tao Han
Zhi-Guang Zhang
Man Li
Feng-Xiang Qi
Ying Zhang
Ying-Lan Ji
author_sort Yong Jiang
title Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
title_short Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
title_full Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
title_fullStr Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
title_full_unstemmed Potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
title_sort potential role of thymosin beta 4 in the treatment of nonalcoholic fatty liver disease
publisher KeAi Communications Co., Ltd.
publishDate 2017
url https://doaj.org/article/a2dc2abff5b64dabb16e2113912d964a
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