miR-33a Mediates the Anti-Tumor Effect of Lovastatin in Osteosarcoma by Targeting CYR61
- PMID: 30466075
- DOI: 10.1159/000495396
miR-33a Mediates the Anti-Tumor Effect of Lovastatin in Osteosarcoma by Targeting CYR61
Abstract
Background/aims: Preventing cell metastasis is an effective therapeutic strategy to treat osteosarcoma and improve prognosis. Statins have been found to have anticancer effects in addition to their cholesterol-lowering action. As a new target of statins, cysteine-rich 61 (CYR61) was recently identified to promote cell migration and metastasis in osteosarcoma. However, the underlying mechanisms mediating the regulation of CYR61 expression by statins remain unknown.
Methods: Human osteosarcoma cell lines MG63 and SaOS2 were used to clarify the effect of lovastatin on CYR61 expression. Real-time PCR was performed to detect mRNA or microRNA (miRNA) levels and western blot was performed to detect protein levels. Cell invasive ability was determined using Transwell assays. Lentivirus encoding CYR61 cDNA or sterol regulatory element-binding protein 2 (SREBP-2) shRNA was used to upregulate CYR61 expression or downregulate SREBP-2 expression. Binding of the CYR61 3' untranslated region (UTR) and miR-33a was analyzed by luciferase reporter assay.
Results: We found that lovastatin treatment decreased CYR61 expression, inhibited cell invasion and altered epithelial-to-mesenchymal-transition (EMT)-related protein expression, while CYR61 overexpression abolished the effect of lovastatin. Moreover, lovastatin increased the expression of SREBP-2 and miR-33a, which were then downregulated by SREBP-2 silencing. Bioinformatics analysis indicated that the CYR61 3'UTR harbored a potential miR-33a binding site and luciferase reporter assay demonstrated that CYR61 was a target of miR-33a in osteosarcoma cells. Furthermore, miR-33a could inhibit cell invasion and alter EMT-related protein expression. SREBP-2 silencing or miR-33a inhibitor upregulated CYR61 expression and reversed the effects of lovastatin on cell invasion and EMT-related proteins.
Conclusion: Our findings suggest lovastatin suppresses osteosarcoma cell invasion through the SREBP-2/miR-33a/CYR61 pathway.
Keywords: CYR61; Cell invasion; Epithelial-to-mesenchymal transition; Lovastatin; Osteosarcoma; SREBP-2; miR-33a.
© 2018 The Author(s). Published by S. Karger AG, Basel.
Similar articles
-
miR-186-5p Functions as a Tumor Suppressor in Human Osteosarcoma by Targeting FOXK1.Cell Physiol Biochem. 2019;52(3):553-564. doi: 10.33594/000000039. Cell Physiol Biochem. 2019. PMID: 30897321
-
Up-regulation of microRNA-491-5p suppresses cell proliferation and promotes apoptosis by targeting FOXP4 in human osteosarcoma.Cell Prolif. 2017 Feb;50(1):e12308. doi: 10.1111/cpr.12308. Epub 2016 Oct 5. Cell Prolif. 2017. PMID: 27704627 Free PMC article.
-
MiR-363 suppresses cell migration, invasion, and epithelial-mesenchymal transition of osteosarcoma by binding to NOB1.World J Surg Oncol. 2020 May 1;18(1):83. doi: 10.1186/s12957-020-01859-y. World J Surg Oncol. 2020. PMID: 32357945 Free PMC article.
-
MicroRNA-33a/b in lipid metabolism – novel “thrifty” models.Circ J. 2015;79(2):278-84. doi: 10.1253/circj.CJ-14-1252. Epub 2015 Jan 8. Circ J. 2015. PMID: 25744742 Review.
-
Regulation of lipid homeostasis by the bifunctional SREBF2-miR33a locus.Cell Metab. 2011 Mar 2;13(3):241-7. doi: 10.1016/j.cmet.2011.02.004. Cell Metab. 2011. PMID: 21356514 Free PMC article. Review.
Cited by
-
Regulation of the Epithelial to Mesenchymal Transition in Osteosarcoma.Biomolecules. 2023 Feb 20;13(2):398. doi: 10.3390/biom13020398. Biomolecules. 2023. PMID: 36830767 Free PMC article. Review.
-
CCN proteins in the musculoskeletal system: current understanding and challenges in physiology and pathology.J Cell Commun Signal. 2021 Dec;15(4):545-566. doi: 10.1007/s12079-021-00631-5. Epub 2021 Jul 6. J Cell Commun Signal. 2021. PMID: 34228239 Free PMC article. Review.
-
Key events in cancer: Dysregulation of SREBPs.Front Pharmacol. 2023 Mar 8;14:1130747. doi: 10.3389/fphar.2023.1130747. eCollection 2023. Front Pharmacol. 2023. PMID: 36969840 Free PMC article. Review.
-
miR-33a inhibits cell growth in renal cancer by downregulation of MDM4 expression.Mol Genet Genomic Med. 2019 Aug;7(8):e833. doi: 10.1002/mgg3.833. Epub 2019 Jun 28. Mol Genet Genomic Med. 2019. PMID: 31250570 Free PMC article.
-
miR-328-3p mediates the anti-tumor effect in osteosarcoma via directly targeting MMP-16.Cancer Cell Int. 2019 Apr 23;19:104. doi: 10.1186/s12935-019-0829-7. eCollection 2019. Cancer Cell Int. 2019. PMID: 31043859 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials