Skip to main content

CORRECTION article

Front. Oncol., 18 March 2024
Sec. Molecular and Cellular Oncology

Corrigendum: miR-31-3p functions as a tumor suppressor by directly targeting GABBR2 in prostate cancer

Sujin Choi&#x;Sujin Choi1†Soonchul Lee&#x;Soonchul Lee1†Young-Hoon HanYoung-Hoon Han2Junwon ChoiJunwon Choi3Isaac KimIsaac Kim4Jusung LeeJusung Lee1Hyun-Ju An*Hyun-Ju An1*
  • 1Department of Orthopaedic Surgery, CHA Bundang Medical Center, CHA University School of Medicine, Pangyo-ro, Republic of Korea
  • 2Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea
  • 3Department of Molecular Science and Technology, Ajou University, Yeongtong-gu, Republic of Korea
  • 4Department of General Surgery, CHA Bundang Medical Center, CHA University School of Medicine, Pangyo-ro, Republic of Korea

A corrigendum on
miR-31-3p functions as a tumor suppressor by directly targeting GABBR2 in prostate cancer

by Choi S, Lee S, Han Y-H, Choi J, Kim I, Lee J and An H-J (2022) Front. Oncol. 12:945057. doi: 10.3389/fonc.2022.945057

In the published article, there was a mistake in Figure 4 as published. The image of LNCap co-transfected with empty vector and control miRNA in Panel C was mistakenly mixed up with the image of the LNCap co-transfected with GABBR2 vector and miR-31-3p in Panel D. The corrected Figure 4 appears below.

Figure 4
www.frontiersin.org

Figure 4 miR-31-3p-induced tumor suppressive functions are associated with downregulation of GABBR2. (A) Restoration of GABBR2, p-ERK and p-JNK protein levels after ectopic expression of Myc-DDK-tagged-GABBR2. DU145, PC-3 and LNCap cells were transfected with a mixture of miR-31-3p (20 nM) and GABBR2 expression vector (4 μg). An unpaired two-tailed Student’s t-test was used to calculate P values. Error bars represent mean ± SEM. *P value < 0.05, **P value < 0.01 and ***P value < 0.001 vs. Cont (n = 3). (B) Ectopic expression of GABBR2 suppresses miR-31-3p-induced apoptosis of DU145, PC-3, and LNCap cells. An unpaired two-tailed Student’s t-test was used to calculate P values. Error bars represent mean ± SEM. ***P value < 0.001 vs. Cont (n = 3). (C, D) Ectopic expression of GABBR2 restores miR-31-3p-mediated inhibition of PC cell migration and invasion. An unpaired two-tailed Student’s t-test was used to calculate P values. Error bars represent mean ± SEM. *P value < 0.05, **P value < 0.01 and ***P value < 0.001 vs. Cont (n = 3).

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: miR-31-3p, GABBR2, prostate cancer, miRNA, tumor suppressor gene

Citation: Choi S, Lee S, Han Y-H, Choi J, Kim I, Lee J and An H-J (2024) Corrigendum: miR-31-3p functions as a tumor suppressor by directly targeting GABBR2 in prostate cancer. Front. Oncol. 14:1395244. doi: 10.3389/fonc.2024.1395244

Received: 03 March 2024; Accepted: 05 March 2024;
Published: 18 March 2024.

Edited and Reviewed by:

Kirill Afonin, University of North Carolina at Charlotte, United States

Copyright © 2024 Choi, Lee, Han, Choi, Kim, Lee and An. 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: Hyun-Ju An, eWtzNDg2YWhqQG5hdmVyLmNvbQ==

These authors have contributed equally to this work

Disclaimer: 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.