Correction Volume 15, Issue 2 pp 595—596
Correction for: Long non-coding RNA DLEUI promotes papillary thyroid carcinoma progression by sponging miR-421 and increasing ROCK1 expression
- 1 Department of Thyroid Surgery, The First Hospital of Jilin University, Changchun 130021, P.R. China
- 2 Department of Division of Interventional Radiology, China-Japan Union Hospital of Jilin University, Changchun 130033, China
- 3 Department of VIP Unit, China-Japan Union Hospital of Jilin University, Changchun 130033, China
- 4 Department of General Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China
- 5 Department of Interventional Therapy, The First Hospital of Jilin University, Changchun 130021, P.R. China
Received: October 10, 2022 Accepted: January 30, 2023 Published: January 31, 2023
https://doi.org/10.18632/aging.204506How to Cite
Copyright: © 2023 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This article has been corrected: The authors found that Figure 5 contains the same graph panel for “Cell apoptosis (%)” in Figures 5D and 5E. They replaced incorrect graph in Figure 5E with the panel corresponding to the wound healing assay graph measuring “Relative migration level (%)” from the original sets of experiments. This correction has no impact on the experimental outcome or conclusions.
Corrected Figure 5 is presented below.
Figure 5. DLEU1 regulates PTC cell growth and progression through the miR-421/ROCK1 axis. (A) Western blot analysis shows ROCK1 protein levels in sh-NC-, sh-DLEU1- and sh-DLEU1 plus miR-421 inhibitor-transfected TPC-1 cells. (B) Spearman correlation analysis shows that ROCK1 mRNA expression is inversely related to DLEU1 expression in PTC tissues (n=54). (C) CCK-8 assay analysis shows proliferation rates of TPC-1 cells transfected with sh-NC, sh-DLEU1, sh-DLEU1 plus miR-421 inhibitor, and sh-DLEU1 plus ROCK1 overexpression plasmid. (D) Flow cytometry analysis shows percentage apoptosis (% Annexin-V+ cells) in TPC-1 cells transfected with sh-NC, sh-DLEU1, sh-DLEU1 plus miR-421 inhibitor, and sh-DLEU1 plus ROCK1 overexpression plasmid. (E) Wound healing assay results show the numbers of migrating cells in the TPC-1 cells transfected with sh-NC, sh-DLEU1, sh-DLEU1 plus miR-421 inhibitor, and sh-DLEU1 plus ROCK1 overexpression plasmid. (F) Transwell invasion assay results show the numbers of invading cells in the TPC-1 cells transfected with sh-NC, sh-DLEU1, sh-DLEU1 plus miR-421 inhibitor, and sh-DLEU1 plus ROCK1 overexpression plasmid. Note: The data is represented as the means ± SD of at least three independent experiments. *P< 0.05 and **P< 0.01.