This article is a correction to:
Long Noncoding RNA NONHSAT079852.2 Contributes to GBM Recurrence by Functioning as a ceRNA for has-mir-10401-3p to Facilitate HSPA1A Upregulation
Ningning Zhao1
Jiajie Zhang1
Lili Zhao1Xiaoni Fu1
Qian Zhao1
Min Chao2Haiyan Cao2
Yang Jiao2
Yaqin Hu2
Chao Chen1*
Liang Wang 2*and 
Huijuan Wang1*- 1College of Life Sciences, Northwest University, Xian, China
- 2Department of Neurosurgery, Tangdu Hospital of Air Force Medical University, Xian, China
By Zhao N, Zhang J, Zhao L, Fu X, Zhao Q, Chao M, Cao H, Jiao Y, Hu Y, Chen C, Wang L and Wang H (2021). 11:636632. doi: 10.3389/fonc.2021.636632
In the original article, there were mistakes in Figure 4 as published. Due to carelessness, we put the wrong picture of Figure 4B, we initially planned to use the results of the third repeated experiment as a representative picture, but in the end we put the picture of the first experiment here. The picture for “shGFP” group in Figure 4C and F were duplication of the images for “Ctrl” group. We had double checked the original data and found that the errors were caused by our carelessness in exporting the representative images and compiling these figures. The corrected Figure 4 appears below.
FIGURE 4
Figure 4 LncRNAs NONHSAT079852.2 can promote the proliferation, invasion and migration of glioma cells. (A) qRT-PCR analysis of HSPA1A in U251(A1) or GBM-W(A2) cells after transfection for 48 hours. (B) Western blot analysis of HSPA1A in U251 or GBM-W cells after transfection for 48 hours. (C) IHC analysis of HSPA1A in U251 or GBM-W cells after transfection for 48 hours. (D) Growth curve of U251(D1) or GBM-W (D2) cells after transfection for 48 hours by CCK8 assay. (E) Proliferation of U251 or GBM-W cells after transfection for two weeks as determined by colony-formation assay. (F) Migration and invasion ability of U251 or GBM-W cells after transfection for 48 hours. (G) Migration of U251(G1) or GBM-W(G2) cells after transfection for 48 hours as detected by wound healing assay. Results were presented as mean ± SD. *p < 0.05, **p < 0.01, NS, not significant.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: recurrent glioblastoma multiforme, RNA-sequencing, lncRNAs, HSPA1A, ceRNA
Citation: Zhao N, Zhang J, Zhao L, Fu X, Zhao Q, Chao M, Cao H, Jiao Y, Hu Y, Chen C, Wang L and Wang H (2021) Corrigendum: Long Noncoding RNA NONHSAT079852.2 Contributes to GBM Recurrence by Functioning as a ceRNA for has-mir-10401-3p to Facilitate HSPA1A Upregulation. Front. Oncol. 11:807421. doi: 10.3389/fonc.2021.807421
Received: 02 November 2021; Accepted: 22 November 2021;
Published: 07 December 2021.
Edited and reviewed by:
Marco Mina, HAYA Therapeutics, SwitzerlandCopyright © 2021 Zhao, Zhang, Zhao, Fu, Zhao, Chao, Cao, Jiao, Hu, Chen, Wang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Huijuan Wang, whj@nwu.edu.cn; Liang Wang, drwangliang@126.com; Chao Chen, cchen898@nwu.edu.cn