Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  AACR Conference on Molecular Diagnostics - 2008
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[Cancer Research 27, 1990-1997, November 1, 1967]
© 1967 American Association for Cancer Research

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Association of Embryonic Antigens with Experimentally Induced Hepatic Lesions in the Rat

M. Stanislawski-Birencwajg, J. Uriel and P. Grabar

Laboratoire de Chimie des Protéines, Institut de Recherches Scientifiques sur le Cancer, CNRS, Villejuif, Seine, France

Short-term hepatic injury was produced in rats by single i.p. injections of N-dimethylnitrosoamine, carbon tetrachloride, and cadmium sulfate, or by partial hepatectomy. In all cases, the animals responded with varying serum titers of embryonic {alpha}2-glycoprotein which could be detected as early as 24 hours after the treatment. Antigen LA, another embryonic constituent, was never detected under the above conditions. Long-term hepatic injury was produced by oral ingestion of carcinogenic aminoazo dyes, N-dimethylnitrosoamine and aflatoxin B1, and by noncarcinogenic analogs of aminoazo dyes. The lesions induced were those classically obtained following such treatments: hepatocarcinoma, bile-duct carcinoma, cirrhosis, hepatitis, etc. The embryonic {alpha}2-glycoprotein was associated with all these lesions, whereas Antigen LA was specifically associated with rats bearing hepatocarcinomas. Neither Antigen LA nor the {alpha}2-glycoprotein were found in rats bearing tumors of other organs than the liver. Lipoprotein-esterase was increased in the majority of sera of rats with these various hepatic lesions.

Received 1/16/67. Accepted 6/16/67.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1967 by the American Association for Cancer Research.