Volume 44, Issue 6 , Pages 482-486, December 2006
The matrix metalloproteinase system in oral squamous cell carcinoma
Abstract
Background
The matrix metalloproteinase (MMP) system is responsible for degradation of tissue in both normal and pathological processes, including tumour invasion and metastasis.
Aim
To compare tissue concentrations of components of the MMP system between tumour tissue and normal tissue in patients with oral squamous cell carcinoma, and to correlate concentrations with pathological grade of tumour.
Methods
Thirty-eight paired tissue samples from tumours and normal tissue were analysed by three laboratory techniques: firstly, enzyme linked immunosorbent assays (ELISA) in ng/mg protein for MMP-1, MMP-3, and tissue inhibitors of metalloproteinases (TIMPs) -1 and -2. Secondly, gelatinase activity assays to measure concentrations of total and endogenous active gelatinases, MMP-2 and MMP-9 (ng/mg protein). And thirdly to use quenched fluorescent substrate hydrolysis to measure total MMP activity (pM/min).
Results
The concentration of all MMPs was significantly higher in tumour than in normal oral tissue (p
<
0.05, Mann–Whitney U-test). Tissue concentrations of some of these factors correlated with clinical and pathological indices of aggressiveness of tumours, including T-stage, N-stage, tumour differentiation, and anatomical level of involved nodes. However, the study was not powered to show statistical significance.
Conclusion
It is the balance between proteinases and their inhibitors that controls tissue degradation at each stage of tumour invasion and metastasis. Measurement of MMPs in oral mucosal biopsy samples may establish the invasive potential of tumours at their initial presentation.
Keywords: Head and neck cancer, Tissue inhibitors of metalloproteinase (TIMP), Proteinases, Proteinase inhibitors, Metastasis
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PII: S0266-4356(05)00322-0
doi:10.1016/j.bjoms.2005.10.005
© 2005 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Inc. All rights reserved.
Volume 44, Issue 6 , Pages 482-486, December 2006
