Esophageal Cancer Development: Crucial Clues Arising from the Extracellular Matrix
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Cells
Abstract
Abstract: 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.