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Free Full-Text
Review
Published: 30 July 2013
(This article belongs to the Section Molecular Pathology)
Abstract: Ovarian
Cancer represents the most fatal type of gynecological malignancies. A
number of processes are involved in the pathogenesis of ovarian cancer,
especially within the tumor microenvironment. Angiogenesis represents a
hallmark phenomenon in cancer, and it is responsible for tumor spread
and metastasis in ovarian cancer, among other tumor types, as it leads
to new blood vessel formation. In recent years angiogenesis has been
given considerable attention in order to identify targets for developing
effective anti-tumor therapies. Growth factors have been identified to
play key roles in driving angiogenesis and, thus, the formation of new
blood vessels that assist in “feeding” cancer. Such molecules include
the vascular endothelial growth factor (VEGF), the platelet derived
growth factor (PDGF), the fibroblast growth factor (FGF), and the
angiopoietin/Tie2 receptor complex. These proteins are key players in
complex molecular pathways within the tumor cell and they have been in
the spotlight of the development of anti-angiogenic molecules that may
act as stand-alone therapeutics, or in concert with standard treatment
regimes such as chemotherapy. The pathways involved in angiogenesis and
molecules that have been developed in order to combat angiogenesis are
described in this paper.
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