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      Expressão imuno-histoquímica das metaloproteinases 2 e 9 não está associada à progressão do carcinoma de células escamosas de esôfago Translated title: Metalloproteinases 2 and 9 immunohistochemistry expression is not associated to esophageal squamous cell carcinoma progression

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          Abstract

          INTRODUÇÃO: O carcinoma de células escamosas do esôfago está entre os tipos mais agressivos de câncer e de pior prognóstico. As metaloproteinases de matriz (MMPs), especialmente as MMP-2 e MMP-9, vêm sendo utilizadas para avaliação prognóstica do câncer, associadas a invasão, tamanho e crescimento tumoral. OBJETIVO: O presente estudo visa investigar as expressões imuno-histoquímicas de MMP-2 e MMP-9, avaliando se existe correlação entre sua expressão e o estadiamento tumoral, invasão vascular, invasão local (pT) e diferenciação tumoral no carcinoma de células escamosas de esôfago. MATERIAL E MÉTODO: Foi realizado um estudo retrospectivo utilizando 31 blocos de parafina contendo tumores de carcinoma escamoso esofágico, obtidas por esofagectomias realizadas entre 1998 e 2003, no Hospital Universitário de Santa Maria (HUSM). Os cortes histológicos foram submetidos à reação imuno-histoquímica, com sistema de amplificação por polímero não-biotinilado Novolink para detecção de MMP-2 e MMP-9. RESULTADOS: A avaliação da MMP-2 apresentou positividade fraca em apenas cinco casos, não demonstrando correlação com as variáveis estudadas. Também não foram observadas associações significativas entre as variáveis do estudo e o grau de expressão imuno-histoquímica da MMP-9. CONCLUSÃO: A expressão imuno-histoquímica das MMP-2 e MMP-9 não parece ser influenciada pelos parâmetros investigados. Nesse sentido, estudos adicionais são necessários para melhor compreensão de sua associação aos fatores prognósticos do carcinoma de células escamosas de esôfago.

          Translated abstract

          INTRODUCTION: Esophageal squamous cell carcinoma is an aggressive malignant neoplasia with poor prognosis. The expression of matrix metalloproteinases (MMPs), mainly 2 and 9, has been used for the prognostic evaluation of cancer in association with tumor invasion, size and tumoral growth analysis. OBJECTIVE: The aim of the present study was to investigate the immunohistochemical expression of MMP-2 and MMP-9 and evaluate if there is an association between their expression and tumor staging, vascular invasion, local invasion (pT) and tumoral differentiation in esophageal squamous cell carcinoma. MATERIAL AND METHODS: We conducted a retrospective study using 31 paraffin-embedded specimens of esophageal squamous cell carcinoma obtained by esophagectomies performed at Santa Maria University Hospital, Rio Grande do Sul State, Brazil between 1998 and 2003. The histological sections were immunohistochemically studied using a non-biotinylated Novolink system for MMP-2 and MMP-9 detection. RESULTS: MMP-2 immunohistochemical expression was detected only in 5 cases and did not demonstrate correlation with the variables analyzed. Furthermore, MMP-9 immunohistochemical expression was not significantly associated with the other variables. CONCLUSION: MMP-2 and MMP-9 immunohistochemical expression does not seem to be influenced by the variables reported in this study. Thus further investigations are required to a better understanding of their association with the prognostic factors of esophageal squamous cell carcinoma.

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          The regulation of matrix metalloproteinases and their inhibitors.

          The matrix metalloproteinases (MMP) are a family of 23 enzymes in man. These enzymes were originally described as cleaving extracellular matrix (ECM) substrates with a predominant role in ECM homeostasis, but it is now clear that they have much wider functionality. Control over MMP and/or tissue inhibitor of metalloproteinases (TIMP) activity in vivo occurs at different levels and involves factors such as regulation of gene expression, activation of zymogens and inhibition of active enzymes by specific inhibitors. Whilst these enzymes and inhibitors have clear roles in physiological tissue turnover and homeostasis, if control of their expression or activity is lost, they contribute to a number of pathologies including e.g. cancer, arthritis and cardiovascular disease. The expression of many MMPs and TIMPs is regulated at the level of transcription by a variety of growth factors, cytokines and chemokines, though post-transcriptional pathways may contribute to this regulation in specific cases. The contribution of epigenetic modifications has also been uncovered in recent years. The promoter regions of many of these genes have been, at least partly, characterised including the role of identified single nucleotide polymorphisms. This article aims to review current knowledge across these gene families and use a bioinformatic approach to fill the gaps where no functional data are available.
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            Estimativa 2008 – Incidência de Câncer no Brasil

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              Gelatinases (MMP-2 and -9) and their natural inhibitors as prognostic indicators in solid cancers.

              Neoplastic growth and dissemination involve increased proteolytic activity that is able to escape the regulative elements. Matrix metalloproteinases (MMPs), particularly gelatinases A and B (MMP-2 and -9), play a role in tumor invasion and angiogenesis, and they participate in cancer progression in several neoplasias. The expression of tissue inhibitors of gelatinases, TIMPs-1 and -2, has also been shown to be associated with the clinical course in some cancers. The prognostic value of these markers, however, seems to vary a great deal in different neoplastic diseases. In this review, the impact of the gelatinases and their inhibitors on the clinical course in several solid cancers is evaluated based on the growing data from recent clinical studies. The clinical data most often explore the overexpression of mRNA or immunoreactive protein in tumor tissue, or measure the concentration of the circulating proteinase or its inhibitor in pretreatment or follow-up serum samples. The growing amount of recent clinical data suggests that the impact of gelatinases on treatment decisions should be tested in clinical trials.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                jbpml
                Jornal Brasileiro de Patologia e Medicina Laboratorial
                J. Bras. Patol. Med. Lab.
                Sociedade Brasileira de Patologia Clínica (Rio de Janeiro )
                1678-4774
                August 2009
                : 45
                : 4
                : 317-323
                Affiliations
                [1 ] Universidade Federal de Santa Maria Brazil
                [2 ] Universidade Luterana do Brasil
                [3 ] Universidade Federal do Rio Grande do Sul
                [4 ] ULBRA
                [5 ] Brigada Militar de Santa Maria
                [6 ] Universidade Federal de Santa Maria Brazil
                Article
                S1676-24442009000400009
                10.1590/S1676-24442009000400009
                93768775-f1ec-4dfd-af54-a5a5135a3a47

                http://creativecommons.org/licenses/by/4.0/

                History
                Product

                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=1676-2444&lng=en
                Categories
                MEDICAL LABORATORY TECHNOLOGY
                MEDICINE, RESEARCH & EXPERIMENTAL
                PATHOLOGY

                Pathology,Medicine,Clinical chemistry
                Esophageal squamous cell carcinoma,Metaloproteinase 9,Metalloproteinase 9,Immunohistochemistry,Carcinoma de células escamosas de esôfago,Metaloproteinase 2,Imuno-histoquímica,Metalloproteinase 2

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