Liver damage in patients with colony-stimulating factor-producing tumors. 1993

A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
Second Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.

OBJECTIVE We have demonstrated that colony-stimulating factor (CSF)-producing tumor cell lines produce not only CSF but also interleukin-1 (IL-1) and interleukin-6 (IL-6). Clinically, we have observed that patients bearing such tumors present with liver dysfunction and fever in addition to marked leukocytosis. The purpose of this study was to determine whether or not the liver damage was specifically related to CSF-producing tumors. METHODS Clinicopathologic examinations were performed in six autopsied patients with CSF-producing tumors. We also transplanted two tumor cell lines (KHC287 and CHU-2), which produce granulocyte (G)-CSF, IL-1, and IL-6, to nude mice. RESULTS Of the six patients, five had G-CSF- and one had granulocyte/macrophage (GM)-CSF-producing tumors. IL-1 and IL-6 concentrations in plasma or culture supernatant were elevated in these patients. Biochemical examinations revealed high serum enzyme levels of the biliary system in contrast to normal or slight increases in transaminase levels in all patients studied. Serum direct bilirubin was elevated in five of the six patients. Three common pathologic changes of the liver were found: (1) focal necrosis associated with neutrophil infiltration in the centrilobular zones, (2) fibrous change and enlargement of the portal area associated with neutrophil infiltration, and (3) intrahepatic cholestasis. The same pathologic changes, except for cholestasis, were reproduced in the liver of mice transplanted with KHC287 or CHU-2. CONCLUSIONS These results indicate that patients with CSF-producing tumors have characteristic liver damage, and suggest a new paraneoplastic syndrome of leukocytosis and liver damage.

UI MeSH Term Description Entries
D007375 Interleukin-1 A soluble factor produced by MONOCYTES; MACROPHAGES, and other cells which activates T-lymphocytes and potentiates their response to mitogens or antigens. Interleukin-1 is a general term refers to either of the two distinct proteins, INTERLEUKIN-1ALPHA and INTERLEUKIN-1BETA. The biological effects of IL-1 include the ability to replace macrophage requirements for T-cell activation. IL-1,Lymphocyte-Activating Factor,Epidermal Cell Derived Thymocyte-Activating Factor,Interleukin I,Macrophage Cell Factor,T Helper Factor,Epidermal Cell Derived Thymocyte Activating Factor,Interleukin 1,Lymphocyte Activating Factor
D007931 Leucyl Aminopeptidase A zinc containing enzyme of the hydrolase class that catalyzes the removal of the N-terminal amino acid from most L-peptides, particularly those with N-terminal leucine residues but not those with N-terminal lysine or arginine residues. This occurs in tissue cell cytosol, with high activity in the duodenum, liver, and kidney. The activity of this enzyme is commonly assayed using a leucine arylamide chromogenic substrate such as leucyl beta-naphthylamide. Cytosol Aminopeptidase,Leucine Aminopeptidase,L-Leucylnaphthylamidase,Methoxyleucine Aminopeptidase,Peptidase S,Zinc-Manganese-Leucine Aminopeptidase,Aminopeptidase, Cytosol,Aminopeptidase, Leucine,Aminopeptidase, Leucyl,Aminopeptidase, Methoxyleucine,Aminopeptidase, Zinc-Manganese-Leucine,Zinc Manganese Leucine Aminopeptidase
D007964 Leukocytosis A transient increase in the number of leukocytes in a body fluid. Pleocytosis,Leukocytoses,Pleocytoses
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008103 Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. Cirrhosis, Liver,Fibrosis, Liver,Hepatic Cirrhosis,Liver Fibrosis,Cirrhosis, Hepatic
D008107 Liver Diseases Pathological processes of the LIVER. Liver Dysfunction,Disease, Liver,Diseases, Liver,Dysfunction, Liver,Dysfunctions, Liver,Liver Disease,Liver Dysfunctions
D008297 Male Males
D008807 Mice, Inbred BALB C An inbred strain of mouse that is widely used in IMMUNOLOGY studies and cancer research. BALB C Mice, Inbred,BALB C Mouse, Inbred,Inbred BALB C Mice,Inbred BALB C Mouse,Mice, BALB C,Mouse, BALB C,Mouse, Inbred BALB C,BALB C Mice,BALB C Mouse
D008819 Mice, Nude Mutant mice homozygous for the recessive gene "nude" which fail to develop a thymus. They are useful in tumor studies and studies on immune responses. Athymic Mice,Mice, Athymic,Nude Mice,Mouse, Athymic,Mouse, Nude,Athymic Mouse,Nude Mouse
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age

Related Publications

A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
May 1983, Cancer research,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
January 1994, Ryoikibetsu shokogun shirizu,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
July 2006, Pathology international,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
November 1982, Experimental hematology,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
June 1995, The American journal of medicine,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
January 1994, Urologia internationalis,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
June 1995, British journal of haematology,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
January 2015, International surgery,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
October 1999, Journal of gastroenterology,
A Suzuki, and T Takahashi, and Y Okuno, and S Seko, and Y Fukuda, and K Nakamura, and M Fukumoto, and Y Konaka, and H Imura
October 2001, American journal of hematology,
Copied contents to your clipboard!