[Corrigendum] Two prostate cancer‑associated polymorphisms in the 3'UTR of IGF1R influences prostate cancer susceptibility by affecting miRNA binding

Wang,Huimin; Huang,Wentao; Yu,Xiaoxiang; Li,Weidong; Huang,Yuanjie; Mo,Zengnan; Gao,Yong; Zhou,Qingniao; Hu,Yanling

doi:10.3892/or.2020.7646

August-2020 Volume 44 Issue 2

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August-2020 Volume 44 Issue 2

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Correction Open Access

[Corrigendum] Two prostate cancer‑associated polymorphisms in the 3'UTR of IGF1R influences prostate cancer susceptibility by affecting miRNA binding

Authors:
- Huimin Wang
- Wentao Huang
- Xiaoxiang Yu
- Weidong Li
- Yuanjie Huang
- Zengnan Mo
- Yong Gao
- Qingniao Zhou
- Yanling Hu
View Affiliations / Copyright

Affiliations: Life Sciences Institute, Guangxi Medical University, Nanning, Guangxi 530021, P.R. China, Pharmaceutical College, Guangxi Medical University, Nanning, Guangxi 530021, P.R. China, Department of Urology, The 303rd Hospital of Chinese People's Liberation Army, Nanning, Guangxi 530021, P.R. China, Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning, Guangxi 530021, P.R. China, Guangxi Colleges and Universities Key Laboratory of Biological Molecular Medicine Research, Nanning, Guangxi 530021, P.R. China

Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Pages: 786-786
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Published online on: June 15, 2020

https://doi.org/10.3892/or.2020.7646
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Oncol Rep 41: [Related article:] 512-524, 2019; DOI: 10.3892/or.2018.6810

Following the publication of the above article, the authors have realized that the way in which the western blotting results were presented in Fig. 6 was not optimal, and that original data should have been included in this figure in order that readers could have understood the content of this paper better.

Figure 6.

Effect of miR-133a, miR-133b or miR-455 overexpression on IGF1R at the mRNA and protein levels. Results for the RT-qPCR and western blot analyses for miR-133a, miR-133b and miR-455 in (A) PC3 and (B) LNCaP cells is shown. RT-qPCR analysis of IGF1R is represented as relative expression in the cells transfected with pre-133a, pre-133b, pre-455 or a scrambled negative control, and the data were analyzed using β-actin as an endogenous control for normalization. The western blots demonstrated the IGF1R protein in the cells transfected with pre-133a, pre-133b, pre-455 or a scrambled negative control. Statistical significance was calculated using a Students t test. ***P<0.001. IGF1R, insulin-like growth factor 1 receptor; miR, microRNA; RT-qPCR, reverse transcription-quantitative polymerase chain reaction; ctrl, control.

The authors regret that these errors were not picked up upon before the article went to print, and apologize to the readership for any confusion these errors may have 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] Two prostate cancer‑associated polymorphisms in the 3'UTR of IGF1R influences prostate cancer susceptibility by affecting miRNA binding

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Figure 6.

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