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CORRECTION article

Front. Oncol., 30 September 2024
Sec. Cancer Genetics

Corrigendum: A novel LncRNA, AC091729.7 promotes sinonasal squamous cell carcinomas proliferation and invasion through binding SRSF2

Boyu Yu&#x;Boyu Yu1†Linmei Qu&#x;Linmei Qu2†Tianyi WuTianyi Wu3Bingrui YanBingrui Yan1Xuan KanXuan Kan1Xuehui ZhaoXuehui Zhao1Like YangLike Yang1Yushan LiYushan Li1Ming LiuMing Liu1Linli TianLinli Tian1Yanan Sun*Yanan Sun1*Qiuying Li*Qiuying Li1*
  • 1Department of Otorhinolaryngology, Head and Neck Surgery, The Second Affiliated Hospital, Harbin Medical University, Harbin, China
  • 2Department of Otorhinolaryngology, Head and Neck Surgery, The Fifth Affiliated Hospital, Harbin Medical University, Daqing, China
  • 3Department of Otorhinolaryngology, Head and Neck Surgery, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, China

A Corrigendum on
A Novel LncRNA, AC091729.7 promotes sinonasal squamous cell carcinomas proliferation and invasion through binding SRSF2

By Yu B, Qu L, Wu T, Yan B, Kan X, Zhao X, Yang L, Li Y, Liu M, Tian L, Sun Y and Li Q (2020). . 9:1575. doi: 10.3389/fonc.2019.01575

In the published article, there was an error in the legend for Figure 3F Transwell invasion assay as published. The corrected Figure 3 and its legend appear below.

Figure 3
www.frontiersin.org

Figure 3. The knockdown of AC091729.7 inhibits the proliferation, migration, and invasion of SNSCC cells. (A) Relative RNA level of AC091729.7 was decreased in SNSCC cells with AC091729.7 knockdown. (B) CCK-8 showed that the viability of SNSCC cells was inhibited after the downregulation of AC091729.7 expression. (C) Colony-formation assay suggested that SNSCC cell proliferation was inhibited after AC091729.7 knockdown. (D) Subcutaneous xenograft SNSCC tumors developed in nude mice after RPMI-2650 cells were transfected with lentivirus encoding (a) AC091729.7 shRNA; (b) control shRNA. (E) Wound healing cell migration assay. (F) Transwell invasion assay (**p < 0.01).

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: long non-coding RNA, AC091729.7, sinonasal squamous cell carcinomas, serine/arginine rich splicing factor 2, prognosis

Citation: Yu B, Qu L, Wu T, Yan B, Kan X, Zhao X, Yang L, Li Y, Liu M, Tian L, Sun Y and Li Q (2024) Corrigendum: A novel LncRNA, AC091729.7 promotes sinonasal squamous cell carcinomas proliferation and invasion through binding SRSF2. Front. Oncol. 14:1476128. doi: 10.3389/fonc.2024.1476128

Received: 05 August 2024; Accepted: 23 August 2024;
Published: 30 September 2024.

Edited and Reviewed by:

Meng Zhou, Wenzhou Medical University, China

Copyright © 2024 Yu, Qu, Wu, Yan, Kan, Zhao, Yang, Li, Liu, Tian, Sun and Li. 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: Yanan Sun, c3luMjc2N0AxMjYuY29t; Qiuying Li, cWl1eWluZzA5MTJAMTYzLmNvbQ==

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.