[Corrigendum] Lycorine inhibits cell proliferation and migration by inhibiting ROCK1/cofilin‑induced actin dynamics in HepG2 hepatoblastoma cells

Liu,Wuyi; Zhang,Qian; Tang,Qin; Hu,Changpeng; Huang,Jingbin; Liu,Yali; Lu,Yanyi; Wang,Qing; Li,Guobing; Zhang,Rong

doi:10.3892/or.2019.7362

December-2019 Volume 42 Issue 6

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December-2019 Volume 42 Issue 6

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Correction Open Access

[Corrigendum] Lycorine inhibits cell proliferation and migration by inhibiting ROCK1/cofilin‑induced actin dynamics in HepG2 hepatoblastoma cells

Authors:
- Wuyi Liu
- Qian Zhang
- Qin Tang
- Changpeng Hu
- Jingbin Huang
- Yali Liu
- Yanyi Lu
- Qing Wang
- Guobing Li
- Rong Zhang
View Affiliations / Copyright

Affiliations: Department of Pharmacy, Xinqiao Hospital, Army Medical University, Chongqing 400037, P.R. China

Copyright: © Liu et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
Pages: 2856-2856
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Published online on: October 10, 2019

https://doi.org/10.3892/or.2019.7362
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Article

Oncol Rep 40: [Related article:] 2298-2306, 2018; DOI: 10.3892/or.2018.6609

After having carefully checked the original data of Fig. 3, the authors noted that the student in their research group had inadvertently selected incorrect images for the 10 and 20 µM lycorine experiments to show the effect of lycorine on the migration of HepG2 cells during the figure compilation process.

Figure 3.

Lycorine inhibits the migration of HepG2 cells. (A) Cells were exposed to serial concentrations of lycorine (10 and 20 μM) for 24 or 48 h. The effects of lycorine on HepG2 cell migration were evaluated by wound healing assay. Scale bar, 200 μm. (B) The effect of lycorine on the migration of HepG2 cells was assessed in a Transwell assay. HepG2 cells were treated with lycorine at 10 or 20 μM for 48 h. Scale bar, 200 μm. (C) Following treatment of HepG2 cells with lycorine (1, 2.5, 5, 10 and 20 μM) for 48 h, western blotting was performed to assess the expression of MMP-9 and MMP-2. The relative quantification of proteins was analyzed using Quantity One software. Data are presented the mean ± standard deviation (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. control. MMP, matrix metalloproteinase.

The corrected version of Fig. 3 is shown. The authors confirm that this error did not influence the statistical analysis shown for the migration of the cells, and neither were the overall results and conclusions of this article affected.

The authors appreciate this opportunity to correct the scientific record, and all authors agree with this correction. Furthermore, the authors apologize for not noticing this error prior to publication, and for any inconvenience caused.