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. 2022 Nov 12;20:528. doi: 10.1186/s12967-022-03749-1

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© The Author(s) 2022

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. 8 — MICAL1 expression was positively correlated with p-TBC1D1 ^Ser660, FZD7 and β-catenin. A Representative immunohistochemical staining of MICAL1, p-TBC1D1^Ser660, FZD7 and β-catenin in sections of pancreatic cancer specimens. B Immunohistochemical analysis of MICAL1, p-TBC1D1.^Ser660, FZD7 and β-catenin expression in specimens from 92 cases of pancreatic cancer. Statistical differences were determined by Chi-squared Test. *, P < 0.05; **, P < 0.01