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. 2023 Aug 1;14:4620. doi: 10.1038/s41467-023-40327-5

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© The Author(s) 2023

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — a Western blotting of CAND1 in liver samples from normal donors (n = 6) and NAFLD patients (n = 7). b CAND1 mRNA level in liver samples from normal donors (n = 6) and NAFLD patients (n = 7). c Western blotting of CAND1 in the livers from HFD-fed and NC-fed mice (n = 6). NC, Normal chow. d The mRNA levels of CAND1 in the livers from HFD-fed and NC-fed mice (n = 7). e Western blotting of CAND1 in AML12 cells treated with PA (n = 4). f CAND1 mRNA level in AML12 cells treated with PA (n = 7). g Western blotting of CAND1 in THLE-2 cells treated with PA (n = 4). h CAND1 mRNA level in THLE-2 cells treated with PA (n = 7). p values obtained via two-tailed unpaired Student’s t tests, one-way ANOVA with Tukey’s multiple comparisons test. The data were shown as means ± SD of independent biological replicates. Source data are provided as a Source data file.