Updating the role of matrix metalloproteinases in mineralized tissue and related diseases.
Cintia Kazuko TokuharaMariana Rodrigues SantessoGabriela Silva Neubern de OliveiraTalita Mendes Oliveira VenturaJulio Toshimi DoyamaWillian Fernando ZambuzziRodrigo Cardoso de OliveiraPublished in: Journal of applied oral science : revista FOB (2019)
Bone development and healing processes involve a complex cascade of biological events requiring well-orchestrated synergism with bone cells, growth factors, and other trophic signaling molecules and cellular structures. Beyond health processes, MMPs play several key roles in the installation of heart and blood vessel related diseases and cancer, ranging from accelerating metastatic cells to ectopic vascular mineralization by smooth muscle cells in complementary manner. The tissue inhibitors of MMPs (TIMPs) have an important role in controlling proteolysis. Paired with the post-transcriptional efficiency of specific miRNAs, they modulate MMP performance. If druggable, these molecules are suggested to be a platform for development of "smart" medications and further clinical trials. Thus, considering the pleiotropic effect of MMPs on mammals, the purpose of this review is to update the role of those multifaceted proteases in mineralized tissues in health, such as bone, and pathophysiological disorders, such as ectopic vascular calcification and cancer.
Keyphrases
- induced apoptosis
- bone regeneration
- papillary thyroid
- bone mineral density
- clinical trial
- healthcare
- cell cycle arrest
- public health
- gene expression
- heart failure
- squamous cell
- squamous cell carcinoma
- soft tissue
- bone loss
- body composition
- working memory
- endoplasmic reticulum stress
- chronic kidney disease
- lymph node metastasis
- cell death
- open label
- oxidative stress
- single cell
- drug induced
- mass spectrometry
- social media
- study protocol