Abstract

Nonalcoholic fatty liver disease (NAFLD) encompasses a spectrum of conditions ranging from hepatic steatosis to inflammation (nonalcoholic steatohepatitis or NASH) with or without fibrosis, in the absence of significant alcohol consumption. The presence of fibrosis in NASH patients is associated with greater liver-related morbidity and mortality; however, the molecular mechanisms underlying the development of fibrosis and cirrhosis in NAFLD patients remain poorly understood. Long non-coding RNAs (lncRNAs) are emerging as key contributors to biological processes that are underpinning the initiation and progression of NAFLD fibrosis. This review summarizes the experimental findings that have been obtained to date in animal models of liver fibrosis and NAFLD patients with fibrosis. We also discuss the potential applicability of circulating lncRNAs to serve as biomarkers for the diagnosis and prognosis of NAFLD fibrosis. A better understanding of the role played by lncRNAs in NAFLD fibrosis is critical for the identification of novel therapeutic targets for drug development and improved, noninvasive methods for disease diagnosis.

Highlights

  • Long non-coding RNAs are emerging as important contributors to biological processes underlying the pathophysiology of human disease [1]

  • We discuss the potential applicability of circulating Long non-coding RNAs (lncRNAs) to serve as biomarkers for the diagnosis and prognosis of Nonalcoholic fatty liver disease (NAFLD) fibrosis based on findings from liver fibrosis that were attributed to non-NAFLD etiologies

  • Nonalcoholic fatty liver disease (NAFLD) encompasses a spectrum of conditions ranging from steatosis to inflammation, fibrosis, cirrhosis, and hepatocellular carcinoma (HCC) [3,4]

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Summary

Introduction

Long non-coding RNAs (lncRNAs) are emerging as important contributors to biological processes underlying the pathophysiology of human disease [1]. While the role of lncRNAs in cancer has been an area of active investigation for many years, the involvement of these molecules in the development of obesity, type 2 diabetes (T2D), and related comorbidities, such as nonalcoholic fatty liver disease (NAFLD), is relatively recent [2]. We discuss the potential applicability of circulating lncRNAs to serve as biomarkers for the diagnosis and prognosis of NAFLD fibrosis based on findings from liver fibrosis that were attributed to non-NAFLD etiologies. Nonalcoholic fatty liver disease (NAFLD) encompasses a spectrum of conditions ranging from steatosis to inflammation, fibrosis, cirrhosis, and hepatocellular carcinoma (HCC) [3,4]. NAFLD is the major cause of chronic liver disease and it is associated with substantial morbidity and

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