Journal of Clinical Pathology 2007;60:483-486
ORIGINAL ARTICLE
Nuclear and cytoplasmic Maspin expression in primary non-small cell lung cancer
1 Institute of Pathology, University of Regensburg, Regensburg, Germany
2 Institute of Pathology, University of Basel, Basel, Switzerland
3 Department of Pathology, University of Vermont College of Medicine, Burlington, Vermont, USA
4 Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
5 Pulmonary Division, Department of Internal Medicine, University of Basel, Basel, Switzerland
Correspondence to:
Dr M Woenckhaus
Institute of Pathology, University of Regensburg, Franz-Josef-Strauss-Allee 11, D-93053 Regensburg, Germany; matthias.woenckhaus{at}klinik.uni-r.de
Aim: To investigate whether nuclear and cytoplasmic Maspin expression is associated with distinct clinicopathological parameters and TP53 expression in a representative series of primary non-small cell lung cancer (NSCLC).
Methods: Tissue microarrays (n = 487) were used to immunohistochemically analyse expression of Maspin and TP53. Cytoplasmic and nuclear expression of Maspin was scored on the basis of the percentage of positive tumour cells. Univariate analysis of clinicopathological variables potentially affecting tumour-specific survival was performed.
Results: Immunohistochemical Maspin expression (nuclear and cytoplasmic) was informative in 72.3% (352/487) of cases. Cytoplasmic and nuclear Maspin immunoreactivity in
10% of tumour cells was detected in 37.8% (133/352) and 65.3% (230/352) of informative cases, respectively. Nuclear and cytoplasmic Maspin staining was observed more frequently in primary squamous cell carcinomas than in other lung cancer types. Only nuclear Maspin immunoreactivity was significantly associated with positive TP53 staining. Cytoplasmic or nuclear Maspin expression was not associated with tumour-specific survival.
Conclusion: Maspin expression was found both in the nucleus and the cytoplasm of NSCLC, more frequently in squamous cell carcinomas. However, no association with tumour-specific survival could be demonstrated.
Abbreviations: IHC, immunohistochemistry; NSCLC, non-small cell lung cancer; TMA, tissue microarray
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
