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. 2020 Dec 10;15:600. doi: 10.1186/s13018-020-02145-z

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© The Author(s) 2020

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — Gene expression of Wnt/b-catenin signal pathway components was analyzed by real-time PCR. The fibroblasts were treated with 100 μM naringin in the presence or absence of 100 ng/ml DKK-1 for 6 h. Transcription of a β-catenin and its target gene b cyclin D1, which participate in the Wnt signaling pathway, were upregulated by naringin treatment, and this upregulation was markedly attenuated by DDK-1 (ap < 0.001 versus control group; bp < 0.001 versus 100 μM naringin group)