Prognostic value of Bmi-1 oncoprotein expression in NSCLC patients: a tissue microarray study

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. M...

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Published inJournal of cancer research and clinical oncology Vol. 134; no. 9; pp. 1037 - 1042
Main Authors Vrzalikova, Katerina, Skarda, Joseph, Ehrmann, Jiri, Murray, Paul G., Fridman, Eduard, Kopolovic, Jury, Knizetova, Petra, Hajduch, Marian, Klein, Jiri, Kolek, Vitezslav, Radova, Lenka, Kolar, Zdenek
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 01.09.2008
Springer
Springer Nature B.V
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Summary: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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ISSN:0171-5216
1432-1335
DOI:10.1007/s00432-008-0361-y