4.5 Article

Matrix metalloproteinase 7 is associated with clinical and pathological characteristics of salivary adenoid cystic carcinomas

Journal

EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
Volume 280, Issue 2, Pages 839-845

Publisher

SPRINGER
DOI: 10.1007/s00405-022-07630-1

Keywords

Palate salivary glands; Adenoid cystic carcinoma; Matrix metalloproteinase-7; Immunohistochemistry; Vascular endothelial growth factor A

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This study investigated the relationship between MMP-7 expression and the clinical and pathological characteristics of SACC. The findings revealed that high MMP-7 expression in SACC samples was associated with tumor differentiation, invasiveness, and clinical stage, and positively correlated with VEGF-A expression.
Objectives The aim of this study was to investigate the relationship between matrix metalloproteinase-7 (MMP-7) expression and the clinical and pathological characteristics of salivary adenoid cystic carcinomas (SACC) of the palatal minor salivary gland. Methods In this study, 58 samples of SACC and 10 samples of normal salivary gland tissue were examined. Immunohistochemistry was used to detect MMP-7 and vascular endothelial growth factor A (VEGF-A) expression in SACC and normal tissues. The clinical and pathological characteristics of the patients with SACC were collected. Results Of the 58 SACC samples, 44 were positive for MMP-7, and the expression rate was 75.9%. No expression was detected in the 10 normal salivary gland tissues. The level of MMP-7 expression in the SACC and normal samples was significantly different. The level of expression of MMP-7 in the SACC samples did not correlate with age, sex or pathological type but did correlate with pathological grade, nerve infiltration and clinical stage. There was a positive correlation between VEGF-A and MMP-7 expression. Conclusions The SACC samples showed high expression of MMP-7, which was associated with tumour differentiation, invasiveness and clinical stage. The detection of MMP-7 positively correlated with the detection of VEGF-A in SACC.

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