Nodal metastasis and survival in oral cancer: Association with protein expression of SLPI, not with LCN2, TACSTD2, or THBS2

ABSTRACT Background Gene expression profiling revealed a strong signature predicting lymph node metastases in oral squamous cell carcinoma (OSCC). Four of the most predictive genes are secretory leukocyte protease inhibitor (SLPI), lipocalin‐2 (LCN2), thrombospondin‐2 (THBS2), and tumor‐associated c...

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Published inHead & neck Vol. 37; no. 8; pp. 1130 - 1136
Main Authors Noorlag, Rob, van der Groep, Petra, Leusink, Frank K. J., van Hooff, Sander R., Frank, Michaël H., Willems, Stefan M., van Es, Robert J. J.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.08.2015
Wiley Subscription Services, Inc
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Summary:ABSTRACT Background Gene expression profiling revealed a strong signature predicting lymph node metastases in oral squamous cell carcinoma (OSCC). Four of the most predictive genes are secretory leukocyte protease inhibitor (SLPI), lipocalin‐2 (LCN2), thrombospondin‐2 (THBS2), and tumor‐associated calcium signal transducer 2 (TACSTD2). This study correlates their protein expression with lymph node metastases, overall survival (OS), and disease‐specific survival (DSS). Methods Two hundred twelve patients with OSCC were included for protein expression analysis by immunohistochemistry. Results SLPI expression correlates with lymph node metastases in the whole cohort, not in a subgroup of cT1 to 2N0. SLPI expression correlates with OS (hazard ratio [HR] = 0.61) and DSS (HR = 0.47) in multivariate analysis. LCN2, THBS2, and TACSTD2 show no correlation with lymph node metastases, OS, or DSS. Conclusion Although SLPI expression correlates with lymph node metastases, it has no additional value in determining lymph node metastases in early oral cancer. However, it is an independent predictor for both OS and DSS and therefore a relevant prognostic biomarker in OSCC. © 2014 Wiley Periodicals, Inc. Head Neck 37: 1130–1136, 2015
Bibliography:ArticleID:HED23716
Stefan M. Willems was funded by the Dutch Cancer Society (clinical fellowship: 2011-4964)
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ISSN:1043-3074
1097-0347
DOI:10.1002/hed.23716