Skip to main content
Log in

The influence of down-regulation of ACP1 by RNAi on the metastasis capability of osteosarcoma cell line MG-63

  • Published:
The Chinese-German Journal of Clinical Oncology

Abstract

Objective

The aim of this study was to study the inhibition effect of small interfering RNAs (siRNA) on gene expression in MG-63 cells, and to study the inhibitory effect on metastasis of MG-63.

Methods

A plasmid of a short hairpin RNA targeting acid phosphatase 1 (ACP1) was constructed and transfected into MG-63 cell line. ACP1 expression of MG-63 cells before and after transfection was detected by RT-PCR and Western blot. The capacity of adhesion, migration and invasion was examined by adhesion assay, migration assay and transwell assay.

Results

The recombinant plasmid pGenesil-1/ACP1-shRNA was successfully constructed. shRNA efficiently inhibited the expression of ACP1 by gene and protein level and suppressed cell migration. The adhesion decreased from 96.41 ± 8.83 to 43.38 ± 6.03 (P < 0.01), invasion ability from 56.5 ± 4.8 to 36.3 ± 6.1 (P < 0.05).

Conclusion

Down-regulating ACP1 by shRNA reduced the capacity of metastasis of MG-63 cell, which providing a novo-approach to biotherapy of cancer.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ferreira CV, Justo GZ, Souza AC, et al. Natural compounds as a source of protein tyrosine phosphatase inhibitors: application to the rational design of small-molecule derivatives. Biochimie, 2006, 88: 1859–1873.

    Article  PubMed  CAS  Google Scholar 

  2. Malentacchi F, Marzocchini R, Gelmini S, et al. Up-regulated expression of low molecular weight protein tyrosine phosphatases in different human cancers. Biochem Biophys Res Commun, 2005, 334: 875–883.

    Article  PubMed  CAS  Google Scholar 

  3. Alho I, Clara Bicho M, Carvalho R, et al. Low molecular weight protein tyrosine phosphatase genetic polymorphism and susceptibility to cancer development. Cancer Genet Cytogenet, 2008, 181: 20–24.

    Article  PubMed  CAS  Google Scholar 

  4. Song DX, Chen AM, Guo FJ, et al. Differential proteomic analysis and function study of human prostate carcinoma cells with different osseous metastatic tendency. Nat Med J China, 2008, 88: 1197–1201.

    CAS  Google Scholar 

  5. Denu JM, Dixon JE. Protein tyrosine phosphatases: mechanisms of catalysis and regulation. Curr Opin Chem Biol, 1998, 2: 633–641.

    Article  PubMed  CAS  Google Scholar 

  6. Raugei G, Ramponi G, Chiarugi P. Low molecular weight protein tyrosine phosphatases: small, but smart. Cell Mol Life Sci, 2002, 59: 941–949.

    Article  PubMed  CAS  Google Scholar 

  7. Hammond SM, Bernstein E, Beach D, et al. An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells. Nature, 2000, 404: 293–296.

    Article  PubMed  CAS  Google Scholar 

  8. Hannon GJ. RNA interference. Nature, 2002, 418: 244–251.

    Article  PubMed  CAS  Google Scholar 

  9. Parri M, Buricchi F, Taddei ML, et al. EphrinA1 repulsive response is regulated by an EphA2 tyrosine phosphatase. J Biol Chem, 2005, 280: 34008–34018.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anmin Chen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhu, B., Chen, A. & Guo, F. The influence of down-regulation of ACP1 by RNAi on the metastasis capability of osteosarcoma cell line MG-63. Chin. -Ger. J. Clin. Oncol. 8, 481–484 (2009). https://doi.org/10.1007/s10330-009-0097-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10330-009-0097-4

Key words

Navigation