Stage-specific embryonic antigen-4 is expressed in basaloid lung cancer and associated with poor prognosis
Basaloid carcinoma represents a rare variant of nonsmall cell lung cancer (NSCLC), which has shown a poor prognosis in a number of studies. Although it is considered to derive from a pluri- or multipotent pulmonary stem cells, little is known about the expression and clinical significance of stem ce...
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| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2013
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| In: |
The European respiratory journal
Year: 2013, Jahrgang: 41, Heft: 3, Pages: 656-663 |
| ISSN: | 1399-3003 |
| DOI: | 10.1183/09031936.00225711 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1183/09031936.00225711 Verlag, Volltext: http://erj.ersjournals.com/content/41/3/656 
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| Verfasserangaben: | Sandra Gottschling, Katrin Jensen, Arne Warth, Felix J. F. Herth, Michael Thomas, Philipp A. Schnabel, Esther Herpel |
MARC
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| 520 | |a Basaloid carcinoma represents a rare variant of nonsmall cell lung cancer (NSCLC), which has shown a poor prognosis in a number of studies. Although it is considered to derive from a pluri- or multipotent pulmonary stem cells, little is known about the expression and clinical significance of stem cell antigens in this variant. Stage-specific embryonic antigen-4 (SSEA-4) was analysed by immunohistochemistry in 38 patients with resected early-stage basaloid NSCLC who had a median follow-up of 72.9 months. The expression of SSEA-4 was related to clinico-pathological characteristics, to the expression of the adult stem cell antigens CD117, CD133 and breast cancer resistance protein 1 (BCRP1), and to prognosis. SSEA-4 was positive in 37% of the specimens and showed no association with clinico-pathological characteristics or the expression of adult stem cell antigens. Cox proportional hazards regression analysis revealed a 6.0-fold increased risk of relapse (p = 0.001) and a 4.2-fold increased risk of disease-related mortality (p = 0.017) in SSEA-4-positive patients, while SSEA-4-negative patients showed a prognosis comparable with that of other early-stage NSCLC. SSEA-4 is expressed in a fraction of basaloid NSCLC and is associated with poor prognosis. | ||
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