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MMP9: A Tough Target for Targeted Therapy for Cancer.
Augoff, Katarzyna; Hryniewicz-Jankowska, Anita; Tabola, Renata; Stach, Kamilla.
Afiliación
  • Augoff K; Department of Surgical Education, Wroclaw Medical University, 50-367 Wroclaw, Poland.
  • Hryniewicz-Jankowska A; Department of Chemistry and Immunochemistry, Wroclaw Medical University, 50-367 Wroclaw, Poland.
  • Tabola R; Deprtment of Cytobiochemistry, Biotechnology Faculty, University of Wroclaw, 50-383 Wroclaw, Poland.
  • Stach K; Department of Thoracic Surgery, Wroclaw Medical University, 50-367 Wroclaw, Poland.
Cancers (Basel) ; 14(7)2022 Apr 06.
Article en En | MEDLINE | ID: mdl-35406619
ABSTRACT
Having the capability to proteolyze diverse structural and signaling proteins, matrix metalloproteinase 9 (MMP9), one of the best-studied secretory endopeptidases, has been identified as a crucial mediator of processes closely associated with tumorigenesis, such as the extracellular matrix reorganization, epithelial to mesenchymal transition, cell migration, new blood vessel formation, and immune response. In this review, we present the current state of knowledge on MMP9 and its role in cancer growth in the context of cell adhesion/migration, cancer-related inflammation, and tumor microenvironment formation. We also summarize recent achievements in the development of selective MMP9 inhibitors and the limitations of using them as anticancer drugs.
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