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. 2024 Nov 20;13(1):40. doi: 10.1038/s41389-024-00542-1

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 2 — The influence of thrombin and rADAM9 (A), rMMP9 alone or in the presence of the MMP inhibitor E3304 (B), and PANC-1 lysate (C) Incubation of ADAM9 bacteria on the percentage of SAPE-positive bacteria. D Fluorescence levels of SAPE-labeled ADAM9 bacteria upon PANC-1 and THP-1 lysate incubation under static conditions as measured by Biotek over time. Data are shown as the mean ± SD of one representative experiment with n = 2, except for (A) and (D), which represent two experiments with n = 2. Two-way ANOVA was used to compare % of events in Q1. Levels of significance: ns not significant, *** p < 0.001, **** p < 0.0001.