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Okay, we're going to move on now and talk about normal cell division because you have to
understand kind of the normal cell pathways that are going to drive cellular proliferation
so that we can understand what goes wrong when we have loss of tumor suppressors or
expansion of oncogenes. So in a normal cell, this is a schematic where a growth factor is
coming in, it is going to bind to and dimerize proteins that are in the membrane. This is
just an example of a kinase, a tyrosine kinase activated receptor. This is a receptor that's
going to have intrinsic tyrosine kinase activity. So that growth factor comes in, it binds
and when it binds by bringing those 2 halves of the receptor together, they now
autophosphorylate each other. Okay. We've changed the confirmation of the protein and
now they acquired those little piece, they've got to have phosphorylation. That's now an
active kinase by virtue of the phosphorylation. And that active kinase will now phosphorylate
a whole bunch of other proteins. And again, I'm specifically not going in to the details
because it's a little bit different for every cell type and every cancer, everything. So,
basically you have growth factor that normally activates the receptors and then that will
phosphorylate additional proteins and in a cascade of phosphorylation we'll eventually get
something that is able to access the nucleus, a transcription factor that's become
phosphorylated that can now sit down on its appropriate promoter site and cause the
transcription of new nuclear material, of new message to drive whatever process we're
going to drive. That's the normal kind of pathway. With the gene transcription, then we
can talk about proliferation, we can talk about making new elements, we can talk about
acquiring some of the other features of a proliferating cell. That gets us into the normal
mitotic pathway and in subsequent talks we will talk about how this goes wrong in
malignancy. And with that, I conclude.