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Prognostic value of Bmi-1 oncoprotein expression in NSCLC patients: a tissue microarray study
K Vrzalikova, J Skarda, J Ehrmann, PG Murray, E Fridman, J Kopolovic, P Knizetova, M Hajduch, J Klein, V Kolek, L Radova, Z Kolar
Jazyk angličtina Země Německo
Grantová podpora
NR8425
MZ0
CEP - Centrální evidence projektů
NLK
PubMed Central
od 1979
ProQuest Central
od 1997-01-01 do 2010-12-31
Medline Complete (EBSCOhost)
od 2003-04-01
Health & Medicine (ProQuest)
od 1997-01-01 do 2010-12-31
Public Health Database (ProQuest)
od 1997-01-01 do 2010-12-31
ROAD: Directory of Open Access Scholarly Resources
od 1997
- MeSH
- čipová analýza proteinů MeSH
- čipová analýza tkání MeSH
- financování organizované MeSH
- imunohistochemie MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- nádory plic metabolismus patologie MeSH
- nemalobuněčný karcinom plic metabolismus patologie MeSH
- prognóza MeSH
- protoonkogenní proteiny genetika metabolismus MeSH
- represorové proteiny genetika metabolismus MeSH
- staging nádorů MeSH
- stanovení celkové genové exprese MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví 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.
Citace poskytuje Crossref.org
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- $a 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.
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