Collagen matrix scaffolds: Future perspectives for the management of chronic liver diseases
Approximately 1.5 billion chronic liver disease (CLD) cases have been estimated worldwide, encompassing a wide range of liver damage severities. Moreover, liver disease causes approximately 1.75 million deaths per year. CLD is typically characterized by the silent and progressive deterioration of li...
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Published in | World journal of clinical cases Vol. 11; no. 6; pp. 1224 - 1235 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Baishideng Publishing Group Inc
26.02.2023
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Subjects | |
Online Access | Get full text |
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Summary: | Approximately 1.5 billion chronic liver disease (CLD) cases have been estimated worldwide, encompassing a wide range of liver damage severities. Moreover, liver disease causes approximately 1.75 million deaths per year. CLD is typically characterized by the silent and progressive deterioration of liver parenchyma due to an incessant inflammatory process, cell death, over deposition of extracellular matrix proteins, and dysregulated regeneration. Overall, these processes impair the correct function of this vital organ. Cirrhosis and liver cancer are the main complications of CLD, which accounts for 3.5% of all deaths worldwide. Liver transplantation is the optimal therapeutic option for advanced liver damage. The liver is one of the most common organs transplanted; however, only 10% of liver transplants are successful. In this context, regenerative medicine has made significant progress in the design of biomaterials, such as collagen matrix scaffolds, to address the limitations of organ transplantation (
low donation rates and biocompatibility). Thus, it remains crucial to continue with experimental and clinical studies to validate the use of collagen matrix scaffolds in liver disease. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Author contributions: All the authors contributed in the writing and revision of manuscript; all authors read and approved the final manuscript. Corresponding author: Gabriela Gutierrez-Reyes, PhD, Academic Research, Professor, Research Scientist, Liver, Pancreas and Motility Laboratory, Unit of Experimental Medicine, School of Medicine, Universidad Nacional Autonoma de Mexico, Hospital General de Mexico, Dr Eduardo Liceaga, Dr. Balmis 148 Col Doctores Cuauhtemoc, Mexico City 06726, Mexico City, Mexico. gabgurey@yahoo.com.mx |
ISSN: | 2307-8960 2307-8960 |
DOI: | 10.12998/wjcc.v11.i6.1224 |