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2. Integrins:
Epithelial cells are connected to the basement membrane through the integrin. Integrins are critical
components of hemidesmosomes (prevent cell motility) which anchor cells to the basement membrane
through interaction with laminins 1 and 5 and are therefore found exclusively on the basal surface of
nontumor cells. Overexpression of several of these molecules has been found in immunohistochemical
studies to correlate with metastatic disease in patients with HNSCC.
3. Laminins:
The laminins are a family of glycoproteins, Laminins are components of the basement membrane and
form hemidesmosomes with integrins to control cell adhesion, motility, polarity, and proliferation.
Laminin-5 has been shown to enhance attachment and lamellopodia formation in tumors cells correlating
with increased migration and invasiveness in vitro. HNSCC tumor cells secrete laminin-5 into their
microenvironment.
4. Cadherins:
The cadherins are members of transmembrane glycoproteins that mediate calcium-dependent cellcell
adhesion. they play important roles in embryogenesis and in the maintenance of normal tissue
architecture. Cadherins are involved in cell recognition, adhesion, and signaling, disruption of cadherin
function has significant implications for the development and behavior of tumors.
6. EpithelialMesenchymal Transition:
The term epithelial-mesenchymal transition (EMT) has been applied to the process of tumorigenesis
corresponding increase in motility and loss of cell adhesion. Presence of EMT was found to be an indicator
of poor prognosis in patients with HNSCC.
8. Matrix Metalloproteinases:
MMPs are proteolytic enzymes requiring metal ions as cofactors. MMPs have been shown to have a role
in invasion and metastasis beyond their ability to degrade ECM components. The substrates for MMPs
include non-ECM proteins including growth factors. The activity of MMPs has been shown to release or
activate basic fibroblast growth factor (bFGF), VEGF, and TGF-, potentially increasing angiogenesis.
10. Serpins:
The serpins are tumor suppressors has been demonstrated in a number of tumor types, including HNSCC.
Loss of Serpin expression has been shown to correlate with lymphatic metastasis and decreased diseasefree survival and overall survival in patients with HNSCC.
11. Angiogenesis:
The formation of new blood vessels is critical for the growth, invasion, and metastasis of tumors. Tumors
>1 mm3 require adequate vasculature to avoid necrosis. Not surprisingly, most tumors overcome this
impediment by stimulating endothelial cell proliferation and new blood vessel formation.
Regulators of Angiogenesis
Vascular Endothelial Growth Factor
VEGF is one of the most potent mediators of tumor angiogenesis, inducing endothelial cell proliferation,
migration, and survival and capillary tube formation.
Interleukin-8
Studies on HNSCC cell lines have shown that IL-8 secreted by tumor cells can induce migration and
invasiveness (323) that may relate to the production of MMP-7 in response to IL-8.
Hypoxia
Areas of very low tissue PO2 (<10 mm Hg) are found to exert a potent selective effect on tumor cells and
to have a pronounced effect on tumor invasiveness and metastatic potential.