Secondary Polycythemia in Male B6C3F1 Mice with Spontaneously Occurring Hepatocellular Carcinomas

Author:

Horinouchi Akira1,Hayashi Shim-Mo2,Ando Takao3,Nonoyama Takashi4

Affiliation:

1. Drug Safety Research Laboratories, Pharmaceutical Development Division, Takeda Chemical Industries, Ltd., 2-17-85 Juso Honmachi, Yodogawa-ku, Osaka 532, Japan,

2. Molecular Pharmacology Laboratories, Pharmaceutical Research Division, Takeda Chemical Industries, Ltd., 2-17-85 Juso Honmachi, Yodogawa-ku, Osaka 532, Japan

3. Drug Safety Research Laboratories, Pharmaceutical Development Division, Takeda Chemical Industries, Ltd., 2-17-85 Juso Honmachi, Yodogawa-ku, Osaka 532, Japan

4. Drug Safety Research Laboratories, Pharmaceutical Development Division, Takeda Chemical Industries, Ltd., 4720 Mitsui, Hikari, Yamaguchi 743, Japan

Abstract

The purpose of this study was to investigate the cause of polycythemia occurring in control male B6C3F, mice with hepatocellular carcinomas from 2-yr carcinogenicity studies. Erythrocyte counts and plasma erythropoietin levels in these mice were significantly increased compared to those in nontumor-bearing mice. Hepatocellular carcinomas in the mice were well differentiated, and the neoplastic hepatocytes contained either or both of 2 types of intracytoplasmic inclusion bodies; one was relatively large and weakly eosinophilic (pale inclusion body), while the other was relatively small and strongly eosinophilic (globular inclusion body). The pale eosinophilic inclusions but not the globular ones were immunohistochemically positive for erythropoietin. Ultrastructurally, the erythropoietin-positive inclusions were characterized by granular materials in dilated cisternae of rough endoplasmic reticulum, suggesting increased protein synthesis. Erythropoietin-negative inclusions were dense bodies that were not surrounded by a delimiting membrane. These findings indicate that polycythemia in hepatocellular carcinoma-bearing mice occurs secondary to excess synthesis and secretion of erythropoietin by neoplastic hepatocytes.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

Reference29 articles.

1. Anemia induces accumulation of erythropoietin mRNA in the kidney and liver.

2. Castle, WB (1985). The polycythemias. In: Hematology , 4th ed. Becker WS (ed). The Massachusetts Institute of Technology Press , Cambridge, Massachusetts, pp. 305-321.

3. Spontaneous neoplasms in B6C3F1 mice

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