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n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor mouse model
BACKGROUND: With 9.1% of all cancer deaths, hepatocellular carcinoma is the second leading cause of cancer deaths worldwide. Due to the increasing prevalence of metabolic syndrome, nonalcoholic fatty liver disease (NAFLD) has evolved into a major risk factor for hepatocellular carcinoma development....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728677/ https://www.ncbi.nlm.nih.gov/pubmed/31523414 http://dx.doi.org/10.1177/2040622319872118 |
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author | Liebig, Marie Dannenberger, Dirk Vollmar, Brigitte Abshagen, Kerstin |
author_facet | Liebig, Marie Dannenberger, Dirk Vollmar, Brigitte Abshagen, Kerstin |
author_sort | Liebig, Marie |
collection | PubMed |
description | BACKGROUND: With 9.1% of all cancer deaths, hepatocellular carcinoma is the second leading cause of cancer deaths worldwide. Due to the increasing prevalence of metabolic syndrome, nonalcoholic fatty liver disease (NAFLD) has evolved into a major risk factor for hepatocellular carcinoma development. Herein, we investigated whether a dietary n-3 polyunsaturated fatty acid (PUFA) supplementation improves the outcome of progressive NAFLD. METHODS: Feeding three high-fat diets, differing in n-3 and n-6 PUFA contents and ratios (n-3/n-6: 1:8, 1:1, 5:1), the impact of n-3 PUFAs and n-3/n-6 PUFA ratios on NAFLD-related liver fibrosis and tumorigenesis was analyzed in 12- and 20-week-old streptozotocin/high-fat diet (STZ/HFD)-treated mice. RESULTS: Feeding of n-3 PUFA-rich diets (1:1 and 5:1) resulted in increased hepatic n-3 PUFA content and n-3/n-6 PUFA ratio with decreased hepatic lipid accumulation. In 20-week-old mice, n-3 PUFA-rich diets alleviated tumor load significantly, with reduced liver/body weight index, tumor size, and tumor number. Finally, these effects were accompanied by a significant improvement of survival of these mice. CONCLUSIONS: Herein, we showed that increased n-3 PUFA content and n-3/n-6 PUFA ratios lead to improved survival and attenuated tumor progression in STZ/HFD-treated mice. Thus, n-3 PUFAs could be the basis for new therapeutic options against NAFLD-related tumorigenesis. |
format | Online Article Text |
id | pubmed-6728677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67286772019-09-13 n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor mouse model Liebig, Marie Dannenberger, Dirk Vollmar, Brigitte Abshagen, Kerstin Ther Adv Chronic Dis Original Research BACKGROUND: With 9.1% of all cancer deaths, hepatocellular carcinoma is the second leading cause of cancer deaths worldwide. Due to the increasing prevalence of metabolic syndrome, nonalcoholic fatty liver disease (NAFLD) has evolved into a major risk factor for hepatocellular carcinoma development. Herein, we investigated whether a dietary n-3 polyunsaturated fatty acid (PUFA) supplementation improves the outcome of progressive NAFLD. METHODS: Feeding three high-fat diets, differing in n-3 and n-6 PUFA contents and ratios (n-3/n-6: 1:8, 1:1, 5:1), the impact of n-3 PUFAs and n-3/n-6 PUFA ratios on NAFLD-related liver fibrosis and tumorigenesis was analyzed in 12- and 20-week-old streptozotocin/high-fat diet (STZ/HFD)-treated mice. RESULTS: Feeding of n-3 PUFA-rich diets (1:1 and 5:1) resulted in increased hepatic n-3 PUFA content and n-3/n-6 PUFA ratio with decreased hepatic lipid accumulation. In 20-week-old mice, n-3 PUFA-rich diets alleviated tumor load significantly, with reduced liver/body weight index, tumor size, and tumor number. Finally, these effects were accompanied by a significant improvement of survival of these mice. CONCLUSIONS: Herein, we showed that increased n-3 PUFA content and n-3/n-6 PUFA ratios lead to improved survival and attenuated tumor progression in STZ/HFD-treated mice. Thus, n-3 PUFAs could be the basis for new therapeutic options against NAFLD-related tumorigenesis. SAGE Publications 2019-09-05 /pmc/articles/PMC6728677/ /pubmed/31523414 http://dx.doi.org/10.1177/2040622319872118 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Liebig, Marie Dannenberger, Dirk Vollmar, Brigitte Abshagen, Kerstin n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor mouse model |
title | n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor
mouse model |
title_full | n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor
mouse model |
title_fullStr | n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor
mouse model |
title_full_unstemmed | n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor
mouse model |
title_short | n-3 PUFAs reduce tumor load and improve survival in a NASH-tumor
mouse model |
title_sort | n-3 pufas reduce tumor load and improve survival in a nash-tumor
mouse model |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728677/ https://www.ncbi.nlm.nih.gov/pubmed/31523414 http://dx.doi.org/10.1177/2040622319872118 |
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