Back to Search Start Over

Overexpression of BMI-1 is associated with poor prognosis in cervical cancer.

Authors :
Tong, Yong-Qing
Liu, Bei
Zheng, Hong-Yun
He, Yu-Juan
Gu, Jian
Li, Feng
Li, Yan
Source :
Asia Pacific Journal of Clinical Oncology; Dec2012, Vol. 8 Issue 4, pe55-e62, 8p
Publication Year :
2012

Abstract

Aim It has been reported that BMI-1, a gene transcription promoter overexpressed in various human cancers, is associated with poor survival. We investigated whether BMI-1 is a marker for cervical cancer by detecting the expression of BMI-1 in cervical cancer. Methods An immunohistochemistry (IHC) streptavidin-peroxidase technique was used to identify BMI-1 protein expression in 302 cervical cancer specimens. Reverse transcription polymerase chain reaction and Western blot were employed to measure BMI-1 mRNA and protein level. The correlation between BMI-1 expression and clinicopathological factors was analyzed. Results Both BMI-1 mRNA and protein expression were evident in cervical carcinoma tissues. An intense positive rate of 55.3% (167/302) was observed by IHC. High BMI-1 expression was correlated with clinical stage, lymph node metastasis, vascular invasion and human papillomavirus (HPV) infection ( P < 0.05), but there is insufficient evidence to confirm its value in tumor size, age, estrogen or progesterone receptor ( P > 0.05). The BMI-1 protein level was positively correlated with the clinical stages of cervical carcinoma and a high BMI-1 expression was associated with poor prognosis ( P < 0.05). Conclusion The high expression of BMI-1 in cervical cancer is related to tumor progression, lymph node metastasis and HPV infection, suggesting that cervical cancer with excessive BMI-1 expression possesses high metastases potential and that BMI-1 may be a promising biomarker for predicting metastasis in cervical cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17437555
Volume :
8
Issue :
4
Database :
Complementary Index
Journal :
Asia Pacific Journal of Clinical Oncology
Publication Type :
Academic Journal
Accession number :
83632982
Full Text :
https://doi.org/10.1111/j.1743-7563.2012.01564.x