Log in

Pin1 expression affects cell proliferation and apoptosis of SW620 cells in colorectal carcinoma

  • Published:
The Chinese-German Journal of Clinical Oncology

Abstract

Objective

The aim of our study was to investigate the effects of Pin1 reduction on SW620 cell proliferation and apoptosis in human colorectal carcinoma.

Methods

We constructed a plasmid of RNA interfering (shRNA) for Pin1 gene (pGenesl-1-Pin1), then the plasmid was transfected into colorectal carcinoma SW620 cells line by liposome mediation. The protein expression of Pin1 was tested by Western blotting. The proliferation rate was analyzed by MTT and the apoptotic rate of cells was tested by flow cytometry. In order to explain further the effect of Pin1 in SW620 cells, the protein level of Bcl-2 was analyzed by Western blotting.

Results

pGenesil-1-Pin1 plasmid was successfully constructed and confirmed by sequencing. The protein relative levels of Pin1 were 0.06 ± 0.04 for the P-shRNA/SW620 cells, and 0.32 ± 0.09 for the P-Con/SW620 cells. The cell growth rate of SW620 cells was slower while the apoptotic rate was increased after transfection with pGenesil-Pin1 plasmid, and the apoptotic rate was 12.38% ± 1.55% for the P-shRNA/SW620 group. At the same time, we found that the protein expression of Bcl-2 was also reduced. The results were 0.13 ± 0.04 for the P-shRNA/SW620 cells, and 0.36 ± 0.08 for the P-Con/SW620 cells.

Conclusion

Inhibited Pin1 expression may suppress the cell proliferation and promote apoptosis of colorectal carcinoma cells in vitro.

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

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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. Weitz J, Koch M, Debus J, et al. Colorectal cancer. Lancet, 2005, 365: 153–165.

    Article  PubMed  Google Scholar 

  2. Rippmann JF, Hobbie S, Daiber C, et al. Phosphorylation-dependent proline isomerization catalyzed by Pin1 is essential for tumor cell survival and entry into mitosis. Cell Growth Differ, 2000, 11: 409–416.

    PubMed  CAS  Google Scholar 

  3. Lu KP, Liou YC, Zhou XZ. Pinning down proline-directed phosphorylation signaling. Trends Cell Biol, 2002, 12: 164–172.

    Article  PubMed  CAS  Google Scholar 

  4. Lu KP, Zhou XZ. The prolyl isomerase Pin1: a pivotal new twist in phosphorylation signalling and disease. Nat Rev Mol Cell Biol, 2007, 8: 904–916.

    Article  PubMed  CAS  Google Scholar 

  5. Liu J, Zhao J, Yang JM. The expression of Pin1, β-catenin and cyclin D1 in elderly lung carcinomas and their significance. Chinese-German J Clin Oncol, 2008, 7: 379–382.

    Article  CAS  Google Scholar 

  6. Mantovani F, Tocco F, Girardini J, et al. The prolyl isomerase Pin1 orchestrates p53 acetylation and dissociation from the apoptosis inhibitor iASPP. Nat Struct Mol Biol, 2007, 14: 912–920.

    Article  PubMed  CAS  Google Scholar 

  7. Yeh ES, Lew BO, Means AR. The loss of PIN1 deregulates cyclin E and sensitizes mouse embryo fibroblasts to genomic instability. J Biol Chem, 2006, 281: 241–251.

    Article  PubMed  CAS  Google Scholar 

  8. Ryo A, Hirai A, Nishi M, et al. A suppressive role of the prolyl isomerase Pin1 in cellular apoptosis mediated by the death-associated protein Daxx. J Biol Chem, 2007, 282: 36671–36681.

    Article  PubMed  CAS  Google Scholar 

  9. Butterfield DA, Abdul HM, Opii W, et al. Pin1 in Alzheimer’s disease. J Neurochem, 2006, 98: 1697–1706.

    Article  PubMed  CAS  Google Scholar 

  10. Xu YX, Manley JL. The prolyl isomerase Pin1 functions in mitotic chromosome condensation. Mol Cell, 2007, 26: 287–300.

    Article  PubMed  CAS  Google Scholar 

  11. Ryo A, Liou YC, Lu KP, et al. Prolyl isomerase Pin1: a catalyst for oncogenesis and a potential therapeutic target in cancer. J Cell Sci, 2003, 116: 773–783.

    Article  PubMed  CAS  Google Scholar 

  12. Blume-Jensen P, Hunter T. Oncogenic kinase signalling. Nature, 2001, 411: 355–365.

    Article  PubMed  CAS  Google Scholar 

  13. Bao L, Kimzey A, Sauter G, et al. Prevalent overexpression of prolyl isomerase Pin1 in human cancers. Am J Pathol, 2004, 164: 1727–1737.

    Article  PubMed  CAS  Google Scholar 

  14. Liu JY, Zhou JN, Chen SQ, et al. Pin1 overexpression in colorectal cancer and its correlation with β-catenin. Acta Univ Med Nan**g (Nat Sci) (Chinese), 2007, 27: 1138–1142.

    CAS  Google Scholar 

  15. Rippmann JF, Hobbie S, Daiber C, et al. Phosphorylation-dependent proline isomerization catalyzed by Pin1 is essential for tumor cell survival and entry into mitosis. Cell Growth Differ, 2000, 11: 409–416.

    PubMed  CAS  Google Scholar 

  16. Li HY, Zhu T, Zhou JH, et al. Short hairpin RNA silences Pin1 and affects proliferation and apoptosis in HeLa cell line. Chin J Obstet Gynecol (Chinese), 2006, 41: 417–421.

    Google Scholar 

  17. Qin LY, Hao H, Li MN, et al. Decreasing Pin1 suppressed the properties of migratory and invasive in colorectal carcinoma SW620 cells. Chinese-German J Clin Oncol, 2010, 9: 216–220.

    Article  Google Scholar 

  18. Hammond SM, Caudy AA, Hannon GJ. Post-transcriptional gene silencing by double-stranded RNA. Nat Rev Genet, 2001, 2: 110–119.

    Article  PubMed  CAS  Google Scholar 

  19. Huang KZ, Cai JC. The principle of RNAi and its application in tumor research. Med Recap (Chinese), 2010, 16: 72–74.

    CAS  Google Scholar 

  20. Kawasaki H, Altieri DC, Lu CD, et al. Inhibition of apoptosis by survivin predicts shorter survival rates in colorectal cancer. Cancer Res, 1998, 58: 5071–5074.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Niuliang Cheng.

Additional information

Supported by grants from the National Natural Science Foundation (No. 81000948/H1606), Natural Science Foundation of Shanxi Province (No. 2010011047-1), and University Science Technology Development Project of Shanxi Province (No. 20091013).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhu, Y., Qin, L., Li, M. et al. Pin1 expression affects cell proliferation and apoptosis of SW620 cells in colorectal carcinoma. Chin. -Ger. J. Clin. Oncol. 10, 100–104 (2011). https://doi.org/10.1007/s10330-011-0737-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10330-011-0737-3

Key words

Navigation