Abstract
Increasing reports suggest that discovery of microRNAs (miRNAs) might provide a novel therapeutical target for human cancers, including osteosarcoma. Previous studies have shown that miR-32 was dysregulated in breast and endometrial cancer. However, its biological roles in osteosarcoma remain unclear. In the current study, we found that miR-32 was significantly down-regulated in osteosarcoma tissues, compared with the adjacent normal tissues. In vitro studies further demonstrated that miR-32 mimics were able to suppress, while its antisense oligos promoted cell proliferation in Saos-2 and U2OS cells. At the molecular level, our data further revealed that expression of Sox9 was negatively regulated by miR-32. Therefore, our results identify an important role for miR-32 in the osteosarcoma through regulating Sox9 expression.
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The Publisher and Editor retract this article in accordance with the recommendations of the Committee on Publication Ethics (COPE). After a thorough investigation we have strong reason to believe that the peer review process was compromised.
An erratum to this article is available at http://dx.doi.org/10.1007/s13277-017-5487-6.
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Supplementary Fig. 1
Expression levels of PTEN in Saos-2 and U2OS cells. (A-B) Protein levels of PTEN were determined by western blot in Saos-2 (A) and U2OS (B) cells transfected with miR-32 mimics or negative controls (NC). (JPEG 81 kb)
Supplementary Fig. 2
Sox9 re-introduction blocks the anti-proliferative roles of miR-32 in U2OS cells. (A) Sox9 protein expression was determined by western blot in U2OS cells. Cells were pre-transfected with miR-32 mimics or negative control (NC) for 24 hr, and then transfected with lentiviruses containing Sox9 gene or empty vector (EV) for another 24 hr. (B-D) The growth curve (B), cell proliferation (BrdU, C) and invasion abilities (D) was determined in U2OS cells. *P < 0.05 **P < 0.01, ***P < 0.001 between two groups. (JPEG 107 kb)
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Xu, JQ., Zhang, WB., Wan, R. et al. RETRACTED ARTICLE: MicroRNA-32 inhibits osteosarcoma cell proliferation and invasion by targeting Sox9. Tumor Biol. 35, 9847–9853 (2014). https://doi.org/10.1007/s13277-014-2229-x
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DOI: https://doi.org/10.1007/s13277-014-2229-x