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Changes in alpha-1 and beta-2 adrenoceptor density in human hepatocellular carcinoma

✍ Scribed by Maurizio Bevilacqua; Guido Norbiato; Enrica Chebat; Gabriella Baldi; Pierluigi Bertora; Tarcisio Vago; Enrico Regalia; Giovanni Colella; Leandro Gennari


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
753 KB
Volume
67
Category
Article
ISSN
0008-543X

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✦ Synopsis


Catecholamines are involved critically in the mechanisms of liver cell proliferation by acting on hepatic alpha-1 and beta-2 adrenoceptors. To identify the role of these receptors in human hepatocellular carcinoma (HCC), the density was examined of alpha-1 and beta-2 adrenoceptors with their affinity and coupling of beta-2 adrenoceptors to adenylate cyclase in HCC tissue and in nonadjacent/nontumor tissue from the same livers. Studies were also done on healthy livers from agematched and sex-matched patients undergoing abdominal surgery for nonhepatic diseases. Twenty-two HCC had a decrease of about 72% in alpha-1 adrenoceptor density compared with their nonadjacent/nontumor tissue and a decrease of about 40% compared with healthy controls. Nonadjacent/nontumor tissue from HCC patients had a 125% increase in alpha-1 adrenoceptor density compared with healthy livers. Twenty-three of 24 HCC had an increase of about 180% in beta adrenoceptor density compared with their nonadjacent/nontumor tissue and healthy controls. Beta adrenoceptors were coupled to adenylate cyclase, as evidenced by a guanosine triphosphate-mediated right shift in (-)-isoproterenol competition isotherms and by cyclic adenosine monophosphate (CAMP) production after stimulation with (-)-isoproterenol. The HCC tissue yielded a larger increase in CAMP than nonadjacent/nontumor tissue and healthy controls. The authors conclude that a higher density of alpha-1 adrenoceptors in nonadjacent/nontumor tissue from HCC characterizes the "healthy" part of the liver in HCC patients and that an increase in beta-2 and a decrease in alpha-1 adrenoceptor densities characterize the tumor part of the liver in human HCC. Cancer 67:2543-2551,1991. N ADULT HUMANS and animals, hepatocytes have long I life spans, ranging from 200 to 400 days or more, but it is a common observation that the proliferation rate of hepatocytes increases after hepatic cell death or loss of liver tissue.' Hepatocyte proliferation occurs in viral hepatitis, cirrhosis, hepatotoxic reactions, and massive liver necrosis.* In turn, viral hepatitis and cirrhosis are strongly associated with hepatocellular carcinoma (HCC), a usually


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