[Corrigendum] lncRNA SNHG3 acts as oncogene in ovarian cancer through miR‑139‑5p and Notch1

Zhang,Li; Li,Guihua; Wang,Xiuzhen; Zhang,Youli; Huang,Xia; Wu,Huazhen

doi:10.3892/ol.2025.15026

June-2025 Volume 29 Issue 6

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June-2025 Volume 29 Issue 6

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Correction Open Access

[Corrigendum] lncRNA SNHG3 acts as oncogene in ovarian cancer through miR‑139‑5p and Notch1

Authors:
- Li Zhang
- Guihua Li
- Xiuzhen Wang
- Youli Zhang
- Xia Huang
- Huazhen Wu
View Affiliations / Copyright

Affiliations: The Obstetric Ward, Jinan Maternal and Child Health Care Hospital, Jinan, Shandong 250001, P.R. China, Department of Clinical Laboratory, Yantaishan Hospital, Yantai, Shandong 264000, P.R. China, Department of Clinical Nutrition, The People's Hospital of Zhangqiu Area, Jinan, Shandong 250200, P.R. China, Department of Cardiology, The People's Hospital of Zhangqiu Area, Jinan, Shandong 250200, P.R. China, Department of Infectious Department, The People's Hospital of Zhangqiu Area, Jinan, Shandong 250200, P.R. China, Department of Gynaecology, Jining No. 1 People's Hospital, Jining, Shandong 272011, P.R. China

Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
Article Number: 280
|
Published online on: April 8, 2025

https://doi.org/10.3892/ol.2025.15026
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Oncol Lett 21: [Related article:] 122, 2021; DOI: 10.3892/ol.2020.12383

Following the publication of the above article, an interested reader drew to the authors’ attention that some of the data panels shown in the scratch wound assays in Fig. 4C and 6C appeared to be overlapping, such that the data may have been derived from a smaller group of original data resources. The authors have re-examined their original data, and realized that a number of errors were made during the compilation of these figures.

Figure 4.

Inhibition of miR-139-5p reverses the suppressive effect of SNHG3 silencing on proliferation and migration. (A) miR-139-5p expression was detected by RT-qPCR in OVCAR3 cells after SNHG3 and miR-139-5p inhibition. (B and C) CCK-8 and wound-healing assays were conducted to detect cell proliferation and migration in OVCAR3 cells with SNHG3 and miR-139-5p inhibition. **P<0.01 and ***P<0.001 compared with si-NC; #P<0.05 and ##P<0.001 compared with the si-SNHG3 group. miR, microRNA; SNHG3, small nucleolar RNA host gene 3; si-SNHG3, small interfering RNA targeting SNHG3; CCK-8, Cell Counting Kit-8; NC, negative control.

Figure 6.

Notch1 overexpression overturns the suppressive effect of SNHG3 knockdown or miR-139-5p overexpression on cell proliferation and migration in OVCAR3 cells. (A) Notch1 expression in OVCAR3 cells. (B and C) Cell proliferation and migration were detected by CCK-8 and wound healing assays. **P<0.01, ***P<0.001 and ****P<0.0001 compared with pc-NC; #P<0.05, ##P<0.01compared with pc-Notch1; $P<0.05, $$P<0.001 compared with the pc-Notch1 + si-SNHG3 group. Notch 1, Notch homolog 1, translocation-associated (Drosophila); SNHG3, small nucleolar RNA host gene 3; miR, microRNA; si-SNHG3, small interfering RNA targeting SNHG3; CCK-8, Cell Counting Kit-8; NC, negative control.

The corrected versions of Figs. 4 and 6 are shown on the next page, featuring data from repeated scratch wound assay experiments for Figs. 4C and 6C. Note that the revisions made to these figures do not affect the overall conclusions reported in the paper. All the authors agree to the publication of this corrigendum. The authors are grateful to the Editor of Oncology Letters for allowing them the opportunity to publish this Corrigendum, and apologize to the readership for any inconvenience caused.

Journals

International Journal of Molecular Medicine

International Journal of Oncology

Molecular Medicine Reports

Oncology Reports

Experimental and Therapeutic Medicine

Oncology Letters

Biomedical Reports

Molecular and Clinical Oncology

World Academy of Sciences Journal

International Journal of Functional Nutrition

International Journal of Epigenetics

Medicine International

[Corrigendum] lncRNA SNHG3 acts as oncogene in ovarian cancer through miR‑139‑5p and Notch1

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