Correction Volume 14, Issue 11 pp 4927—4928
Correction for: ZNF139/circZNF139 promotes cell proliferation, migration and invasion via activation of PI3K/AKT pathway in bladder cancer
- 1 Department of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China
- 2 Human Genetics Resource Preservation Center of Hubei Province, Wuhan, 430071, China
- 3 Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China
Received: April 17, 2022 Accepted: May 29, 2022 Published: June 14, 2022
https://doi.org/10.18632/aging.204132How to Cite
Copyright: © 2022 Yao 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.
Original article: Aging. 2020; 12:9915–9934.
This article has been corrected: The authors noticed errors in Figure 6. As a result of misfiling the data, the images in panel 6C showing UC3 cells transfected with si1- and si2-circZNF139 were the same as the images in panel 6D showing 5637 cells transfected with si1- and si2-circZNF139. The authors corrected panels 6C and 6D in Figure 6 by using representative images from the original sets of experiments. Similarly, the images of cells obtained 48 h after si1-- and si2-circZNF139 transfection were mixed up during preparation of panel 6F and replaced. The images showing invasion by UC3 cells transfected with si1- and si2-ZNF139 were replaced in panel 6G, as was the image of 5637 cells transfected with 3.1 in panel 6H. All images were derived from the initial sets of experiments. The authors stated that these alterations do not affect the results or conclusions of this work and apologized for any inconvenience caused.
New Figure 6 is presented below.
Figure 6. Cell proliferation, clone, migration, and invasion of UC3 and 5637 cells were evaluated after ZNF139/circZNF139 overexpression or knockdown. (A–B) CCK8 assay was employed to assess the proliferation of UC3 and 5637 cells with ZNF139/circZNF139 overexpression or knockdown. (C–D) Crystal violet staining was used to examine the colony formation of UC3 and 5637 cells with ZNF139/circZNF139 overexpression or knockdown. (E–F) Scratch wound healing assay was employed to evaluate the migration of UC3 and 5637 cells with ZNF139/circZNF139 overexpression or knockdown. Images of cell migration at 0 and 48 h transfection are shown at a magnification of 40×. (G–H) Transwell assay was used to analyze the invasion of UC3 and 5637 cells with ZNF139/circZNF139 overexpression or knockdown. Images are representative of the cells invading one field at a magnification of 100×. *, P<0.05; **, P<0.01. ZNF139, zinc finger with KRAB and SCAN domains 1; circ, circular; h, hour.