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. 2022 Mar 16;22:74. doi: 10.1186/s12906-022-03526-z

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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. 7 — a Pg extract (10, 25, and 50 μg/mL) activity on MCF-7 human breast adenocarcinoma cells migration and proliferation potential. Progression of cell migration was monitored by imaging the scratch line initially and at 24 h post-stimulation. Images were taken by light microscopy at 10× magnification; b Pg extract (75, 100, and 150 μg/mL) activity on MCF-7 human breast adenocarcinoma cells migration and proliferation potential. c The anti-migratory potential of Pg extract (10, 25, 50, 75, 100 and 150 μg/mL) on MCF-7 breast adenocarcinoma cells. The bar graphs are expressed as percentage of scratch closure after 24 h compared to the initial surface. Comparison among groups was made using One-way ANOVA test and Dunnett’s multiple comparison post-test. (*** p < 0.001 vs. Control)