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. 2018 Nov 21;8:17210. doi: 10.1038/s41598-018-35496-z

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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FGF19-M52 analogue protects Abcb4^−/− mice from age-related liver damage and HCC progression. qPCR of hepatic (a) Cyp7a1 (b) Cyp8b1. Expression was normalized to Cyclophillin. (c) BA composition (CA/MCA Ratio) in murine plasma and liver. (d) Macroscopic appearance of livers, normalized tumor number and maximum tumor size of 16-months-old Abcb4^−/− mice (n = 14–24). (e) Biochemical parameters of liver damage in 16 months old Abcb4^−/− mice. Statistical significance (*p < 0.05, **p < 0.01, ***p < 0.001) was assessed by Mann-Whitney’s U test.