Prognostic value of Bmi-1 oncoprotein expression in NSCLC patients: a tissue microarray study
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Protein Array Analysis MeSH
- Tissue Array Analysis MeSH
- Immunohistochemistry MeSH
- Nuclear Proteins genetics metabolism MeSH
- Humans MeSH
- Lung Neoplasms metabolism pathology MeSH
- Carcinoma, Non-Small-Cell Lung metabolism pathology MeSH
- Polycomb Repressive Complex 1 MeSH
- Prognosis MeSH
- Proto-Oncogene Proteins genetics metabolism MeSH
- Repressor Proteins genetics metabolism MeSH
- Neoplasm Staging MeSH
- Gene Expression Profiling MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- BMI1 protein, human MeSH Browser
- Nuclear Proteins MeSH
- Polycomb Repressive Complex 1 MeSH
- Proto-Oncogene Proteins MeSH
- Repressor Proteins MeSH
PURPOSE: Bmi-1 is a Polycomb group member which participates in many physiological processes as well as in a wide spectrum of cancers. The aim of this study was to investigate Bmi-1 expression in non-small cell lung cancer (NSCLC) in respect to clinicopathological features and therapeutic outcomes. METHODS: Immunohistochemical staining for Bmi-1 was performed on tissue microarrays (TMAs) constructed from 179 formalin-fixed and paraffin-embedded NSCLC samples (106 squamous, 58 adeno-, and 15 large cell carcinomas). Data were subject to statistical analysis by SPSS. RESULTS: Overall evaluation of all tumor cases showed that 20 (11.43%) were negative, 37 (21.14%) showed weak, 65 (37.14%) moderate and 57 (32.57%) strong nuclear positivity for Bmi-1. Statistical analysis of our data revealed that the expression of Bmi-1 was significantly higher in stage III (P = 10(-6)) and stage IV (P = 10(-5)) tumors compared to stages I and II tumors. The administration of adjuvant chemotherapy significantly increased DFS at stage I and II patients who did not express Bmi-1 when compared to their Bmi-1 positive counterparts (P = 0.05). CONCLUSIONS: Our results suggest that Bmi-1 is significantly associated with progression of NSCLC and might serve as a prognostic marker of adverse disease outcome.
References provided by Crossref.org
Targeted BMI1 inhibition impairs tumor growth in lung adenocarcinomas with low CEBPα expression