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作为一种代谢沉默剂和肝脏肿瘤抑制因子。

as a metabolic silencer and liver tumor suppressor.

作者信息

Wang Lijun, Wang Yu-Shiuan, Mugiyanto Eko, Chang Wei-Chiao, Yvonne Wan Yu-Jui

机构信息

Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, CA.

The College of Life Science, Yangtze University, Jingzhou, Hubei.

出版信息

Liver Res. 2020 Jun;4(2):74-80. doi: 10.1016/j.livres.2020.06.001. Epub 2020 Jun 9.

Abstract

With obesity rate consistently increasing, a strong relationship between obesity and fatty liver disease has been discovered. More than 90% of bariatric surgery patients also have non-alcoholic fatty liver diseases (NAFLDs). NAFLD and non-alcoholic steatohepatitis (NASH), which are the hepatic manifestations of metabolic syndrome, can lead to liver carcinogenesis. Unfortunately, there is no effective medicine that can be used to treat NASH or liver cancer. Thus, it is critically important to understand the mechanism underlying the development of these diseases. Extensive evidence suggests that microRNA 22 () can be a diagnostic marker for liver diseases as well as a treatment target. This review paper focuses on the roles of in metabolism, steatosis, and liver carcinogenesis. Literature search is limited based on the publications included in the PubMed database in the recent 10 years.

摘要

随着肥胖率持续上升,肥胖与脂肪性肝病之间的紧密关系已被发现。超过90%的减肥手术患者也患有非酒精性脂肪性肝病(NAFLD)。NAFLD和非酒精性脂肪性肝炎(NASH)作为代谢综合征的肝脏表现,可导致肝癌发生。不幸的是,目前尚无可用于治疗NASH或肝癌的有效药物。因此,了解这些疾病发生发展的潜在机制至关重要。大量证据表明,微小RNA 22()可作为肝脏疾病的诊断标志物以及治疗靶点。本综述文章聚焦于其在代谢、脂肪变性和肝癌发生中的作用。文献检索基于近10年PubMed数据库收录的出版物,范围有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5f/7523703/fb81bbbce8d1/nihms-1631416-f0001.jpg

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