[Corrigendum] Loss of E‑cadherin promotes prostate cancer metastasis via upregulation of metastasis‑associated gene 1 expression

Fan,Liangsheng; Wang,Hongyan; Xia,Xi; Rao,Yumei; Ma,Xiangyi; Ma,Ding; Wu,Peng; Chen,Gang

doi:10.3892/ol.2020.11421

April-2020 Volume 19 Issue 4

Full Size Image

Journals

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

Medicine International

An International Open Access Journal Devoted to General Medicine.

April-2020 Volume 19 Issue 4

Full Size Image

Correction Open Access

[Corrigendum] Loss of E‑cadherin promotes prostate cancer metastasis via upregulation of metastasis‑associated gene 1 expression

Authors:
- Liangsheng Fan
- Hongyan Wang
- Xi Xia
- Yumei Rao
- Xiangyi Ma
- Ding Ma
- Peng Wu
- Gang Chen
View Affiliations / Copyright

Affiliations: Cancer Biology Medical Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China, Department of Obstetrics and Gynecology, South Mountain Hospital of Guangdong Medical College, Shenzhen, Guangdong 518000, P.R. China, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China

Copyright: © Fan et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
Pages: 3359-3359
|
Published online on: February 28, 2020

https://doi.org/10.3892/ol.2020.11421
Expand metrics +

Article

Oncol Lett 4: [Related article:] 1225-1233, 2012; DOI: 10.3892/ol.2012.934

Subsequently to the publication of the above paper, the authors were alerted to the fact that some of the experimental images featured in Fig. 3C had been selected inappropriately. Specifically, the images presented for the ‘Mock’ and ‘Control siRNA’ experiments had appeared in another article published by the same authors. These errors occurred during the preparation of the manuscript, and were attributed to the inadvertent mislabelling of images or folders.

Figure 3.

Downregulation of E-cadherin affects cell adhesion, invasion ability and cytoskeleton construction. Cells were transfected with E-cadherin siRNA or negative control siRNA for 48 h, and the adhesive ability was examined by MTT assay. All experiments were repeated three times. (A) The adhesion ability to solid phase was significantly downregulated in cells treated with E-cadherin siRNA. *P<0.05 compared with non-treated cells (mock) and negative control siRNA transfected cells. (B) Invasion ability was assessed using the Matrigel™-coated transwell system. 8×103 cells/well were placed in a Matrigel-coated Boyden chamber and allowed to invade for 24 h. Graph reveals the quantification of invasive cells from the lower side of the transwell inserts. *P<0.05 compared with non-treated cells (mock) and negative control siRNA transfected cells. (C) Representative images of invasion experiments. (D) The altered structure (600-fold) of the cytoskeleton was detected using confocal microscopy. Red fluorescent staining represents the α-tubulin, and blue staining represents the nucleus. siRNA, small interfering RNA; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

The corrected version of Fig. 3, showing the correct data for the ‘Mock’ and ‘Control siRNA’ experiments, is shown opposite. Note that these errors in the data selection for this figure did not seriously affect the overall conclusions reported in the study. The authors are grateful to the Editor for granting them the opportunity to publish this Corrigendum, and apologize to the readership of the Journal 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] Loss of E‑cadherin promotes prostate cancer metastasis via upregulation of metastasis‑associated gene 1 expression

This article is mentioned in:

Article

Figure 3.

Related Articles