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Spatial Genomics: Mapping Human Steatotic Liver Disease

Overview
Specialty Gastroenterology
Date 2024 Apr 23
PMID 38654090
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Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD, formerly known as non-alcoholic fatty liver disease) is a leading cause of chronic liver disease worldwide. MASLD can progress to metabolic dysfunction-associated steatohepatitis (MASH, formerly known as non-alcoholic steatohepatitis) with subsequent liver cirrhosis and hepatocellular carcinoma formation. The advent of current technologies such as single-cell and single-nuclei RNA sequencing have transformed our understanding of the liver in homeostasis and disease. The next frontier is contextualizing this single-cell information in its native spatial orientation. This understanding will markedly accelerate discovery science in hepatology, resulting in a further step-change in our knowledge of liver biology and pathobiology. In this Review, we discuss up-to-date knowledge of MASLD development and progression and how the burgeoning field of spatial genomics is driving exciting new developments in our understanding of human liver disease pathogenesis and therapeutic target identification.

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References
1.
Rinella M, Lazarus J, Ratziu V, Francque S, Sanyal A, Kanwal F . A multisociety Delphi consensus statement on new fatty liver disease nomenclature. J Hepatol. 2023; 79(6):1542-1556. DOI: 10.1016/j.jhep.2023.06.003. View

2.
Paik J, Golabi P, Younossi Y, Mishra A, Younossi Z . Changes in the Global Burden of Chronic Liver Diseases From 2012 to 2017: The Growing Impact of NAFLD. Hepatology. 2020; 72(5):1605-1616. DOI: 10.1002/hep.31173. View

3.
Paik J, Golabi P, Younossi Y, Saleh N, Nhyira A, Younossi Z . The Growing Burden of Disability Related to Chronic Liver Disease in the United States: Data From the Global Burden of Disease Study 2007-2017. Hepatol Commun. 2021; 5(5):749-759. PMC: 8122384. DOI: 10.1002/hep4.1673. View

4.
Loomba R, Friedman S, Shulman G . Mechanisms and disease consequences of nonalcoholic fatty liver disease. Cell. 2021; 184(10):2537-2564. DOI: 10.1016/j.cell.2021.04.015. View

5.
Younossi Z, Loomba R, Rinella M, Bugianesi E, Marchesini G, Neuschwander-Tetri B . Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Hepatology. 2017; 68(1):361-371. PMC: 6508084. DOI: 10.1002/hep.29724. View