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We have partially characterized the circulating insulin components from a patient with islet cell carcinoma. The proinsulin-like component is larger in size, less reactive by radioimmunoassay, and more reactive by bioassay than identical preparations from a non-tumor patient. The insulin component is less reactive by radioimmunoassay but otherwise indistinguishable from the non-tumor component. These unique circulating insulin components either represent a specific mutation in an individual patient or a more general heterogeneity of the insulin components in disease states.
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Görden et al. (1971) studied this question.
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