Transplantable pancreatic acinar carcinoma

John R. Warren*, Janardan K Reddy

*Corresponding author for this work

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Fragments of the nafenopin‐induced pancreatic acinar cell carcinoma of rat have been examined in vitro for patterns of intracellular protein transport and carbamylcholine‐induced protein discharge. Continuous incubation of the fragments with [3H]‐leucine for 60 minutes resulted in labeling of rough endoplasmic reticulum, Golgi cisternae, and mature zymogen granules, revealed by electron microscope autoradiography. This result indicates transport of newly synthesized protein from the rough endoplasmic reticulum to mature zymogen granules in approximately 60 minutes. The secretagogue carbamylcholine induced the discharge of radioactive protein by carcinoma fragments pulse‐chase labeled with [3H]‐leucine. A maximal effective carbamylcholine concentration of 10−5 M was determined. The acinar carcinoma resembles normal exocrine pancreas in the observed rate of intracellular protein transport and effective secretagogue concentration. However, the acinar carcinoma fragments demonstrated an apparent low rate of carbamylcholine‐induced radioactive protein discharge as compared with normal pancreatic lobules or acinar cells. It is suggested that the apparent low rate of radioactive protein discharge reflects functional immaturity of the acinar carcinoma. Possible relationships of functional differentiation to the heterogeneous cytodifferentiation of the pancreatic acinar carcinoma are discussed.

Original languageEnglish (US)
Pages (from-to)1535-1542
Number of pages8
JournalCancer
Volume47
Issue number6 S
DOIs
StatePublished - Jan 1 1981

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ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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