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. 2020 Jun 18;20:189. doi: 10.1186/s12906-020-02986-5

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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. 2 — Apoptosis and cell cycle of PVE and GLC by cell flow cytometry analysis. The HUMC Cells were treated with varying PVE concentrations of 0, 0.25, 0.5, 0.75, and 1.0 × IC50 (2.6 mg/ml) or GLC concentrations of 4.65 mg/ml. After 24 h treatment, the cells were analyzed by Annexin V and PI staining. Percentages of cells in both early and late apoptosis were counted (a: apoptosis; b: apoptosis rate, compared with the blank group, ^#p < 0.05, compared with the GLC group, *p < 0.05; c: cell cycle)