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      MMP-9 and MMP-2 gelatinases and TIMP-1 and TIMP-2 inhibitors in breast cancer: correlations with prognostic factors

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          Abstract

          The goal of our study was to analyse the prognostic values for some matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs) in breast cancer. We evaluated the activity and the expression levels of MMP-9, MMP-2, TIMP-1 and TIMP-2 in malignant versus benign fresh breast tumor extracts. For this purpose, gelatinzymography, immunoblotting and ELISA were used to analyse the activity and expression of MMPs and TIMPs. We found that MMP-9 expression level and activity are increased in malignant tumors. In addition, MMP-9/TIMP-1 and MMP-2/TIMP-2 ratio values obtained by us were significantly different in malignant tumors compared to benign tumors. We suggest that the abnormal MMP-9/TIMP-1 balance plays a role in the configuration of breast invasive carcinoma of no special type and also in tumor growth, while altered MMP-2/TIMP-2 ratio value could be associated with lymph node invasion and used as a prognostic marker in correlation with Nottingham Prognostic Index. Finally, we showed that in malignant tumors high expression of estrogen receptors is associated with enhanced activity of MMP-2 and increased bcl-2 levels, while high expression of progesterone receptors is correlated with low TIMP-1 protein levels.

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          Most cited references54

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          Matrix metalloproteinases.

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            Matrix metalloproteinases: they're not just for matrix anymore!

            The matrix metalloproteinases (MMPs) have been viewed as bulldozers, destroying the extracellular matrix to permit normal remodeling and contribute to pathological tissue destruction and tumor cell invasion. More recently, the identification of specific matrix and non-matrix substrates for MMPs and the elucidation of the biological consequence of cleavage indicates that perhaps MMPs should be viewed more as pruning shears, playing sophisticated roles in modulating normal cellular behavior, cell-cell communication and tumor progression.
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              Prognostic factors in breast cancer. College of American Pathologists Consensus Statement 1999.

              Under the auspices of the College of American Pathologists, a multidisciplinary group of clinicians, pathologists, and statisticians considered prognostic and predictive factors in breast cancer and stratified them into categories reflecting the strength of published evidence. Factors were ranked according to previously established College of American Pathologists categorical rankings: category I, factors proven to be of prognostic import and useful in clinical patient management; category II, factors that had been extensively studied biologically and clinically, but whose import remains to be validated in statistically robust studies; and category III, all other factors not sufficiently studied to demonstrate their prognostic value. Factors in categories I and II were considered with respect to variations in methods of analysis, interpretation of findings, reporting of data, and statistical evaluation. For each factor, detailed recommendations for improvement were made. Recommendations were based on the following aims: (1) increasing uniformity and completeness of pathologic evaluation of tumor specimens, (2) enhancing the quality of data collected about existing prognostic factors, and (3) improving patient care. Factors ranked in category I included TNM staging information, histologic grade, histologic type, mitotic figure counts, and hormone receptor status. Category II factors included c-erbB-2 (Her2-neu), proliferation markers, lymphatic and vascular channel invasion, and p53. Factors in category III included DNA ploidy analysis, microvessel density, epidermal growth factor receptor, transforming growth factor-alpha, bcl-2, pS2, and cathepsin D. This report constitutes a detailed outline of the findings and recommendations of the consensus conference group, organized according to structural guidelines as defined.
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                Author and article information

                Journal
                J Cell Mol Med
                J. Cell. Mol. Med
                jcmm
                Journal of Cellular and Molecular Medicine
                John Wiley & Sons, Ltd (Chichester, UK )
                1582-1838
                1582-4934
                April 2006
                01 May 2007
                : 10
                : 2
                : 499-510
                Affiliations
                [a ]Department of Immunology, “Cantacuzino” National Institute for Microbiology and Immunology Bucharest, Romania
                [b ]“Trestioreanu” National Institute of Oncology Bucharest, Romania
                [c ]“Victor Babeş” National Institute of Pathology and Biomedical Science Bucharest, Romania
                Author notes
                * Correspondence to: Dr. Cristiana MATACHE Department of Immunology, “Cantacuzino” National Institute for Microbiology and Immunology, Splaiul Independentei 103, Bucharest 050096, Romania. Tel: ++40(21)3184410 (252); Fax: ++40(21)3184414 E-mail: reg@ 123456cantacuzino.ro
                Article
                10.1111/j.1582-4934.2006.tb00415.x
                3933137
                16796815
                081d003e-b1d4-4597-8991-b0bb08d99923
                History
                : 22 December 2005
                : 20 April 2006
                Categories
                Phenomenin Review Series

                Molecular medicine
                breast cancer,mmp-9,mmp-2,timp-1,timp-2,clinicopathological markers
                Molecular medicine
                breast cancer, mmp-9, mmp-2, timp-1, timp-2, clinicopathological markers

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