The tumor microenvironment is recognized as a key factor in themultiple stages of cancer progression,mediating
local resistance, immune-escape andmetastasis. Cancer growth and progression require remodeling of the tumor
stromal microenvironment, such as the development of tumor-associated blood vessels, recruitment of bone
marrow-derived cells and cytokine processing. Extracellular matrix breakdown achieved by proteases like the fibrinolytic
factor plasmin and matrix metalloproteases is necessary for cell migration crucial for cancer invasion
andmetastasis. Key components of the fibrinolytic system are expressed in cells of the tumormicroenvironment.
Plasmin can control growth factor bioavailability, or the regulation of other proteases leading to angiogenesis,
and inflammation. In this review, we will focus on the role of the fibrinolytic systemin the tumor microenvironment
summarizing our current understanding of the role of the fibrinolytic factors for themodulation of the local
chemokine/cytokine milieu, resulting in myeloid cell recruitment, which can promote neoangiogenesis.