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Oncology Reports
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Print ISSN: 1021-335X Online ISSN: 1791-2431
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August-2023 Volume 50 Issue 2

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

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

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

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

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

Experimental and Therapeutic Medicine

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

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

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

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

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

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Correction Open Access

[Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway

  • Authors:
    • Xiong Shu
    • Huiqi Liu
    • Rui Zhen
    • Yongsheng Jie
    • Lei Chen
    • Hui Qi
    • Chao Wang
    • Renxian Wang
    • Dafu Chen
    • Yuliang Ran
  • View Affiliations / Copyright

    Affiliations: Laboratory of Bone Tissue Engineering, Beijing Laboratory of Biomedical Materials, Beijing Research Institute of Orthopaedics and Traumatology, Beijing JiShuiTan Hospital, Beijing 100035, P.R. China, Department of Basic Medical Science, Medical School of Qinghai University, Xining, Qinghai 810016, P.R. China, State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, P.R. China
    Copyright: © Shu et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
  • Article Number: 156
    |
    Published online on: June 21, 2023
       https://doi.org/10.3892/or.2023.8593
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Article

Oncol Rep 44: [Related article:] 313–324, 2020; DOI: 10.3892/or.2020.7597

Following the publication of the article, a concerned reader drew to the authors' attention that, in Fig. 1B and C on p. 316, two pairs of the data panels showing the results from invasion and migration assay experiments appeared to be overlapping, such that they would have been derived from the same original sources where they were intended to show the results from different experiments; moreover, on p. 1698, the ‘17-AAG / MG-63’ data panels in Fig. 3B and C were also overlapping, albeit the images were presented at a different scale and in a slightly different orientation.

Figure 1.

Osteosarcoma sarcosphere cells exhibit stem-like properties and chemotherapy resistance. (A) The spheroid-forming abilities of sarcosphere and monolayer cells derived from the MG-63 and Saos-2 cell lines were determined using low-attachment plates during methylcellulose culture Scale bar, 50 µm. (B) The migratory capacity of sarcosphere and monolayer cells derived from the MG-63 and Saos-2 cell lines was determined using a Transwell migration assay. (C) The invasive capacity of sarcosphere and monolayer cells derived from the MG-63 and Saos-2 cell lines was determined using a Matrigel invasion assay. (D) Treatment with methotrexate or cisplatin chemotherapy compared with DMSO. Data are presented as the mean ± standard deviation of three independent experiments. **P<0.01, ***P<0.001. MTX, methotrexate.

Figure 3.

17-AAG suppresses stem cell-like properties and chemoresistance of osteosarcoma sarcosphere cells. (A) The spheroid-forming abilities of sarcosphere cells derived from the MG-63 and Saos-2 cell lines were analyzed following treatment with 50 nM 17-AAG using low-attachment plates during methylcellulose culture. Scale bar, 50 µm. (B) The migration capacity of sarcosphere cells derived from MG-63 and Saos-2 cells was determined in 17-AAG-treated cells using a Transwell migration assay. (C) The invasion capacity of sarcosphere cells derived from the MG-63 and Saos-2 cell lines following treatment with 17-AAG was determined using a Matrigel invasion assay. (D) Treatment with methotrexate or cisplatin chemotherapy compared with DMSO following treatment with 17-AAG. Data are presented as the mean ± standard deviation of three independent experiments. **P<0.01, ***P<0.001.

After having examined their original data, the authors have realized that these figures were inadvertently assembled incorrectly. The corrected versions of Figs. 1 and 3, now showing the correct data in Fig. 1C (where the errors made in compiling the figure had occurred) and the correct data for the ‘17-AAG / MG-63’ data panel in Fig. 3C, are shown on the next two pages. These corrections do not grossly affect either the results or the conclusions reported in this work. The authors all agree to the publication of this Corrigendum, and are grateful to the Editor of Oncology Reports for granting them the opportunity to correct the errors that were made during the assembly of these figures. Lastly, the authors apologize to the readership for any inconvenience these errors may have caused.

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Copy and paste a formatted citation
Spandidos Publications style
Shu X, Liu H, Zhen R, Jie Y, Chen L, Qi H, Wang C, Wang R, Chen D, Ran Y, Ran Y, et al: [Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway. Oncol Rep 50: 156, 2023.
APA
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H. ... Ran, Y. (2023). [Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway. Oncology Reports, 50, 156. https://doi.org/10.3892/or.2023.8593
MLA
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H., Wang, C., Wang, R., Chen, D., Ran, Y."[Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway". Oncology Reports 50.2 (2023): 156.
Chicago
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H., Wang, C., Wang, R., Chen, D., Ran, Y."[Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway". Oncology Reports 50, no. 2 (2023): 156. https://doi.org/10.3892/or.2023.8593
Copy and paste a formatted citation
x
Spandidos Publications style
Shu X, Liu H, Zhen R, Jie Y, Chen L, Qi H, Wang C, Wang R, Chen D, Ran Y, Ran Y, et al: [Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway. Oncol Rep 50: 156, 2023.
APA
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H. ... Ran, Y. (2023). [Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway. Oncology Reports, 50, 156. https://doi.org/10.3892/or.2023.8593
MLA
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H., Wang, C., Wang, R., Chen, D., Ran, Y."[Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway". Oncology Reports 50.2 (2023): 156.
Chicago
Shu, X., Liu, H., Zhen, R., Jie, Y., Chen, L., Qi, H., Wang, C., Wang, R., Chen, D., Ran, Y."[Corrigendum] Hsp90 inhibitor 17‑AAG inhibits stem cell‑like properties and chemoresistance in osteosarcoma cells via the Hedgehog signaling pathway". Oncology Reports 50, no. 2 (2023): 156. https://doi.org/10.3892/or.2023.8593
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