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We develop a model for the early stages of malignant tumour invasion dueto random motility, cellular proliferation, proteolysis and haptotaxis.At early times in the absence of tumour cell diffusion, a compressedtumour layer is evident. Transient protease production-decay dynamicsand diffusion, must be present in order for the tumour concentrationpeak to be smoothed to realistic levels. We demonstrate...
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