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Expressions of survivin, P16INK4a, COX-2, and Ki-67 in cervical cancer progression reveal the potential clinical application


  • W.Q. Zhou1,*,
  • Q.Y. Sheng2
  • Y.H. Sheng3
  • W.J. Hou2
  • G.X. Xu2
  • Y.M. Wu3
  • H. Lu2

1Department of Gynecology, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China

2Department of Obstetrics and Gynecology, Central Hospital of Fengxian District, Shanghai, China

3Department of Pathology, Central Hospital of Fengxian District, Shanghai , China

DOI: 10.12892/ejgo2567.2015 Vol.36,Issue 1,February 2015 pp.62-68

Published: 10 February 2015

*Corresponding Author(s): W.Q. Zhou E-mail: zhouweiqiangzwq@hotmail.com

Abstract

Purpose of investigation: To explore the significance of survivin, P16INK4a, COX-2, and Ki-67 expressions for prediction of cervical cancer progression. Materials and Methods: A retrospective study was performed in 129 cases including 24 squamous carcinoma of the cervix (SCC), 70 cervical intraepithelial neoplasias (CIN), 15 cervical condyloma acuminatum (CCA), ten chronic cervicitis (CC), and ten normal cervix (NC). Protein expressions were evaluated using immunohistochemistry. Results: Survivin, P16INK4a; COX-2, and Ki- 67 were highly expressed in SCC and CIN compared with others. Their expression rates were gradually increased in CIN I, CIN II, CIN III, and SCC groups, showing 72.00%, 88.00%, 90.00%, and 95.83% for P16INK4a, 68.00%, 84.00%, 95.00% and 100.00% for COX-2, 76.00%, 96.00%, 100.00%, and 100.00 for Ki-67, respectively. There were significant correlations between survivin and P16INK4a, COX-2, Ki-67, as well as P16INK4a and Ki-67. Conclusion: Survivin, P16INK4a, COX-2 and Ki-67 play critical roles for development and progression of cervical cancer.

Keywords

Cervical cancer; Survivin; P16INK4a; Cyclooxygenase-2; Ki-67; Immunohistochemistry.

Cite and Share

W.Q. Zhou,Q.Y. Sheng,Y.H. Sheng,W.J. Hou,G.X. Xu,Y.M. Wu,H. Lu. Expressions of survivin, P16INK4a, COX-2, and Ki-67 in cervical cancer progression reveal the potential clinical application. European Journal of Gynaecological Oncology. 2015. 36(1);62-68.

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