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The on-demand, limited release of PDGF at a wound site

triggers cell division of neighboring cells for a limited

amount of time, until the PDGF is degraded. This is

different from the continuous release of PDGF from mutant

cells, where PDGF is made in an uncontrolled way at high

levels. Moreover, the mutant cells that make PDGF often

inappropriately express their own PDGF receptor, so

that they can stimulate their own proliferation, thereby

promoting the development of cancer

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