Publications by authors named "Miri Moas"

Metalloproteinases (MMPs) are proteolytic enzymes that function in the extracellular matrix to degrade connective tissues. While it is clear that exercise-induced injury in skeletal muscle promotes increased expression of MMPs, the relationship between exercise intensity and expression of MMPs in muscles is unknown. These experiments tested the hypothesis that exercise-induced expression of matrix metalloproteinases (MMP-2 and MMP-9) is dose-dependent such that high-intensity endurance exercise increases MMP expression whereas low-intensity endurance exercise will not promote MMP expression in skeletal muscles.

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Matrix metalloproteinases (MMPs) are a family of zinc- dependent proteolytic enzymes that function mainly in the extracellular matrix, where they contribute to the development, functioning, and pathology of a wide range of tissues. This mini-review describes the MMPs and tissue inhibitors of MMPs (TIMPs) in skeletal muscle, and considers their involvement in muscle development, ischemia, myonecrosis, angiogenesis, denervation, exercise-induced injuries, disuse atrophy, muscle repair and regeneration, and inflammatory myopathies and dystrophies. Despite the very limited information currently available on MMPs and their inhibitors in skeletal muscle, it is becoming increasingly clear that they have important physiological functions in maintenance of the integrity and homeostasis of muscle fibers and of the extracellular matrix.

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Article Synopsis
  • The p53 tumor suppressor protein is crucial for preventing cancer, as it is often mutated in human cancers, highlighting its role as a key defense mechanism.
  • p53 operates within a complex network of signaling pathways that include feedback loops with other proteins, notably beta-catenin and Akt, which influence its activity and overall cell fate.
  • Disruption of the balance between p53, Mdm2, beta-catenin, and Akt due to genetic alterations can impair p53's tumor suppressor functions, contributing to cancer development.
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Article Synopsis
  • p53 is a crucial tumor suppressor protein that plays a key role in cancer defense, as it is often genetically altered in human cancers.
  • Recent research highlights p53's involvement in a complex network of signaling pathways, particularly through autoregulatory feedback loops that involve other proteins like beta catenin and Akt.
  • The interplay between p53 and Mdm2 is central to these loops, with each component influencing the other's activity, and imbalances in this system due to genetic alterations can undermine p53's protective effects, promoting cancer development.
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