Abstract

The aim of this study was to evaluate the association of the chromobox homologue 7 (CBX7) expression with the epithelial–mesenchymal transition in cervical cancer (CC), as well as with the disease prognosis. CBX7, E-cadherin (E-cad), and vimentin (VIM) expression levels were detected with immunohistochemistry. The relationship between the expression of CBX7, E-cad, and VIM expression and conventional clinicopathological characteristics of CC were evaluated. The positive expression rates of CBX7 and E-cad in the CC tissues were lower than the adjacent non-tumorous cervical tissues. Moreover, the VIM expression level was higher. The CBX7 expression was positively correlated with the E-cad expression, whereas was negatively correlated with the VIM expression. Furthermore, CBX7 was associated with the disease clinical staging, histological differentiation, lymph node metastasis, and vascular invasion. Patients with negative CBX7 expression showed decreased overall survival rates compared with those with low or high CBX7 expression. Multivariate Cox regression analysis indicated that the decreased CBX7 expression was an independent predictor for the poor prognosis of CC. In conclusion, the absence of CBX7 is associated with the histologic differentiation, lymphatic metastasis, vascular invasion, and poor prognosis of CC. CBX7 may be an independent prognostic factor for the prognosis of CC patients.

Highlights

  • Cervical cancer (CC) is one of the most common gynecological malignant diseases, and the fourth most frequent cancer in the world [1,2]

  • Our results showed that chromobox homologue 7 (CBX7) expression was significantly

  • The CBX7 overexpression has been associated with the poor prognosis of the ovarian adenocarcinomas through inhibiting the TRAIL-induced apoptotic pathway, suggesting the carcinogenic effects of CBX7 [8]

Read more

Summary

Introduction

Cervical cancer (CC) is one of the most common gynecological malignant diseases, and the fourth most frequent cancer in the world [1,2]. The mortality of CC has declined in recent years, there are more than 5,00,000 new cases of CC, and CC causes more than 2,50,000 deaths each year. The CC morbidity and the total death cases continue to increase [1], and the 5-year survival rate of CC is only 68% [3], with the tumor metastasis as one of the main causes for death. Previous studies have shown that chromobox homologue 7 (CBX7) is ubiquitously expressed in glioma, endometrium, and other diseases, which may play a role in anticarcinogenesis. The expression levels of CBX7 are reduced in some tumors, and it is correlated with the clinicopathological parameters of several tumors, including breast cancer, bladder cancer, colon cancer, and glioma [4,5,6,7]

Objectives
Methods
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call