A Higher Angiogenin Expression is Associated With a Nonnuclear Maspin Location in Laryngeal Carcinoma.
- Author:
Andrea LOVATO
1
;
Marco LIONELLO
;
Alberto STAFFIERI
;
Stella BLANDAMURA
;
Giulia TEALDO
;
Luciano GIACOMELLI
;
Claudia STAFFIERI
;
Gino MARIONI
Author Information
- Publication Type:Original Article
- Keywords: Laryngeal Neoplasms; Angiogenin; SERPIN-B5; Intracellular Space; Prognosis
- MeSH: Carcinoma, Squamous Cell; Cytoplasm; Disease-Free Survival; Humans; Intracellular Space; Laryngeal Neoplasms; Models, Statistical; Multivariate Analysis; Prognosis; Recurrence
- From:Clinical and Experimental Otorhinolaryngology 2015;8(3):268-274
- CountryRepublic of Korea
- Language:English
- Abstract: OBJECTIVES: In numerous malignancies, angiogenin (ANG) and Maspin are important proangiogenic and antiangiogenic regulators, respectively. The aim of this study was to identify potential relationships between the biological roles of these two proteins in laryngeal squamous cell carcinoma (LSCC). METHODS: Immunohistochemical staining for ANG and Maspin was performed on specimens from 76 consecutive LSCC patients treated with surgery alone, considering the subcellular pattern of Maspin expression. Univariate and multivariate statistical models were used for prognostic purposes. RESULTS: On univariate analysis, a different level of ANG expression was seen for patients stratified by subcellular Maspin expression pattern: the mean ANG expression was higher in cases with a nonnuclear MASPIN expression than in those with a nuclear pattern (P=0.002). Disease-free survival (DFS; in months) differed significantly when patients were stratified by N stage (P=0.01). Patients whose Maspin expression was nonnuclear (i.e., it was cytoplasmic or there was none) had a significantly higher recurrence rate (P<0.001), and shorter DFS (P=0.01) than those with a nuclear Maspin pattern. The mean ANG expression was significantly higher in cases with loco-regional recurrent disease (P=0.007); and patients with an ANG expression > or =5.0% had a significantly shorter DFS than those with an ANG expression <5.0% (P=0.007). On multivariate analysis, ANG expression > or =5.0% was a significant, independent, negative prognostic factor in terms of DFS (P=0.041). CONCLUSION: Our results support the hypothesis that a higher ANG expression is associated with a nonnuclear Maspin expression pattern in patients with LSCC. Further studies are needed to clarify the relationship between the ANG and Maspin pathways, and their potential diagnostic and therapeutic role in LSCC.
