Skip to main content

Advertisement

Log in

The expression and significance of cyclin B1 and survivin in human non-small cell lung cancer

  • Published:
The Chinese-German Journal of Clinical Oncology

Abstract

Objective

We studied the expression of cyclin B1 and survivin in human non-small cell lung cancer (NSCLC), and the relationship between such expression and clinicopathological features of NSCLC.

Methods

One hundred cases of tissue specimen including NSCLC, neighboring noncancerous tissue and normal lung tissue were collected at random. These specimens were detected by immunohistochemical methods.

Results

The expression of cyclin B1 and survivin showed significant difference (P < 0.01) between NSCLC tissues, proliferating epithelial cells of bronchioles and small bronchi in neighboring noncancerous tissues, and normal lung tissues. Compared with normal lung tissues, there was an overexpression of cyclin B1 and survivin in NSCLC and an enhancing expression of cyclin B1 and survivin in proliferating epithelial cells of bronchioles and small bronchi in neighboring noncancerous tissues. Significantly positive correlation was found between the overexpression of cyclin B1 and that of survivin in 100 NSCLC cases (P < 0.01). The significantly positive correlation was also found between the enhancing expression of cyclin B1 and that of survivin in proliferating epithelial cells of bronchioles and small bronchi in neighboring noncancerous tissues (P < 0.01). No statistical significance was found between the different histological types, the differentiated degree, lymphatic metastasis and the expression of cyclin B1 and survivin (P > 0.05) in NSCLC. Statistical significance was marked between different clinical stages of NSCLC and the expression of cyclin B1 and survivin (P < 0.05).

Conclusion

The overexpression of cyclin B1 and survivin was found in NSCLC. The expression of cyclin B1 and survivin might be up-regulated during an early step of tumorigenesis and during the development of NSCLC. The progression of cell cycle could be efficiently connected with the control of apoptosis by the interrelations between the overexpression of cyclin B1 and that of survivin in NSCLC during the G2/M phase. The overexpression of cyclin B1 and survivin might be used as marker in showing the dividing and proliferating ability, and the inhibiting apoptosis ability (lengthening cell lifespan) of NSCLC. Moreover, the overexpression of cyclin B1 and survivin was associated with the clinic stages of NSCLC.

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. Hunter T, Pines J. Cyclins and cancer. II: Cyclin D and CDK inhibitors come of age. Cell, 1994, 79: 573–582.

    Article  PubMed  CAS  Google Scholar 

  2. Wang WW, Li GF, Hong ZP, et al. The expression of survivin in lung adenocarcinoma: a comparative study in Xuanwei and Kunming. Chinese-German J Clin Oncol, 2010, 9: 625–627.

    Article  CAS  Google Scholar 

  3. Altieri DC. The molecular basis and potential role of survivin in cancer diagnosis and therapy. Trends Mol Med, 2001, 7: 542–547.

    Article  PubMed  CAS  Google Scholar 

  4. Satoh K, Kaneko K, Hirota M, et al. Expression of survivin is correlated with cancer cell apoptosis and is involved in the development of human pancreatic duct cell tumors. Cancer, 2001, 92: 271–278.

    Article  PubMed  CAS  Google Scholar 

  5. Rodríguez JA, Span SW, Ferreira CG, et al. CRM1-mediated nuclear export determines the cytoplasmic localization of the antiapoptotic protein Survivin. Exp Cell Res, 2002, 275: 44–53.

    Article  PubMed  Google Scholar 

  6. Skoufias DA, Mollinari C, Lacroix FB, et al. Human survivin is a kinetochore-associated passenger protein. J Cell Biol, 2000, 151: 1575–1582.

    Article  PubMed  CAS  Google Scholar 

  7. O’Connor DS, Grossman D, Plescia J, et al. Regulation of apoptosis at cell division by p34cdc2 phosphorylation of survivin. Proc Natl Acad Sci U S A, 2000, 97: 13103–13107.

    Article  PubMed  Google Scholar 

  8. Zhao J, Tenev T, Martins LM, et al. The ubiquitin-proteasome pathway regulates survivin degradation in a cell cycle-dependent manner. J Cell Sci, 2000, 113: 4363–4371.

    PubMed  CAS  Google Scholar 

  9. Li F, Ambrosini G, Chu EY, et al. Control of apoptosis and mitotic spindle checkpoint by survivin. Nature, 1998, 396: 580–584.

    Article  PubMed  CAS  Google Scholar 

  10. Kallio MJ, Nieminen M, Eriksson JE. Human inhibitor of apoptosis protein (IAP) survivin participates in regulation of chromosome segregation and mitotic exit. FASEB J, 2001, 15: 2721–2723.

    PubMed  CAS  Google Scholar 

  11. Verdecia MA, Huang H, Dutil E, et al. Structure of the human antiapoptotic protein survivin reveals a dimeric arrangement. Nat Struct Biol, 2000, 7: 602–608.

    Article  PubMed  CAS  Google Scholar 

  12. Tamm I, Wang Y, Sausville E, et al. IAP-family protein survivin inhibits caspase activity and apoptosis induced by Fas (CD95), Bax, caspases, and anticancer drugs. Cancer Res, 1998, 58: 5315–5320.

    PubMed  CAS  Google Scholar 

  13. Kuttler F, Valnet-Rabier MB, Angonin R, et al. Relationship between expression of genes involved in cell cycle control and apoptosis in diffuse large B cell lymphoma: a preferential survivin-cyclin B link. Leukemia, 2002, 16: 726–735.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhiyong Li.

Additional information

Supported by a grant from the Science and Technology Department of Liaoning Province (No. 2010225034).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, G., Liu, X., Zhang, D. et al. The expression and significance of cyclin B1 and survivin in human non-small cell lung cancer. Chin. -Ger. J. Clin. Oncol. 10, 192–197 (2011). https://doi.org/10.1007/s10330-011-0771-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10330-011-0771-1

Key words

Navigation