Esophageal Cancer Development: Crucial Clues Arising from the Extracellular Matrix

dc.TypeArticlept_BR
dc.contributor.authorPalumbo Júnior, Antonio
dc.contributor.authorPontes, Bruno
dc.contributor.authorOliveira, Felipe Leite de
dc.contributor.authorCodeço, Matheus Lohan
dc.contributor.authorPinto, Luis Felipe Ribeiro
dc.contributor.authorNasciutti, Luiz Eurico
dc.contributor.authorCosta, Nathalia de Oliveira Meireles da
dc.date.accessioned2022-05-18T13:22:30Z
dc.date.available2022-05-18T13:22:30Z
dc.date.issued2020
dc.description.abstractAbstract: In the last years, the extracellular matrix (ECM) has been reported as playing a relevant role in esophageal cancer (EC) development, with this compartment being related to several aspects of EC genesis and progression. This sounds very interesting due to the complexity of this highly incident and lethal tumor, which takes the sixth position in mortality among all tumor types worldwide. The well-established increase in ECM stiffness, which is able to trigger mechanotransduction signaling, is capable of regulating several malignant behaviors by converting alteration in ECM mechanics into cytoplasmatic biochemical signals. In this sense, it has been shown that some molecules play a key role in these events, particularly the different collagen isoforms, as well as enzymes related to its turnover, such as lysyl oxidase (LOX) and matrix metalloproteinases (MMPs). In fact, MMPs are not only involved in ECM stiffness, but also in other events related to ECM homeostasis, which includes ECM remodeling. Therefore, the crucial role of distinct MMPs isoform has already been reported, especially MMP-2, -3, -7, and -9, along EC development, thus strongly associating these proteins with the control of important cellular events during tumor progression, particularly in the process of invasion during metastasis establishment. In addition, by distinct mechanisms, a vast diversity of glycoproteins and proteoglycans, such as laminin, fibronectin, tenascin C, galectin, dermatan sulfate, and hyaluronic acid exert remarkable effects in esophageal malignant cells due to the activation of oncogenic signaling pathways mainly involved in cytoskeleton alterations during adhesion and migration processes. Finally, the wide spectrum of interactions potentially mediated by ECM may represent a singular intervention scenario in esophageal carcinogenesis natural history and, due to the scarce knowledge on the cellular and molecular mechanisms involved in EC development, the growing body of evidence on ECM’s role along esophageal carcinogenesis might provide a solid base to improve its management in the future.pt_BR
dc.identifier.issn2073-4409
dc.identifier.other10.3390/cells9020455
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/6970
dc.language.isoenpt_BR
dc.publisherCellspt_BR
dc.subjectExtracellular Matrixpt_BR
dc.subjectMatriz Extracelularpt_BR
dc.subjectEsophageal Neoplasmspt_BR
dc.subjectNeoplasias Esofágicaspt_BR
dc.subjectEsophageal Cancerpt_BR
dc.subjectCáncer de Esófagopt_BR
dc.subject.otherEsophageal Carcinogenesisen
dc.subject.otherStiffnessen
dc.subject.otherRemodelingen
dc.titleEsophageal Cancer Development: Crucial Clues Arising from the Extracellular Matrixpt_BR

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