The establishment recently of a transplantable pancreatic acinar carcinoma of rat in our laboratory1, provides a suitable model system to analyze morphogenetic, enzymic and functional differentiation in transformed secretory epithelial cells. Morphologic analysis of this tumor has revealed a continuum of neoplastic cells from those which totally lack mature secretory granules to cells with abundant, well-formed secretory granules. This tumor is easily dissociable into single cells and these cells are found to be more susceptible to agglutination by concanavalin A than the normal pancreatic acinar cells2.
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