Cancer Research Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine  Susan G. Komen for the Cure-AACR Outstanding Investigator Award for Breast Cancer Research
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 Cell Growth & Differentiation

[Cancer Research 26, 221-228, February 1, 1966]
© 1966 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kitagawa, M.
Right arrow Articles by Pressman, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kitagawa, M.
Right arrow Articles by Pressman, D.

In Vivo Localization of Anticarcinogen Antibody in Organs of Carcinogen-treated Rats1

Masayasu Kitagawa2, Yasuo Yagi, Jakob Planinsek and David Pressman

Department of Biochemistry Research, Roswell Park Memorial Institute,3 Buffalo, New York

Rabbit antibody against the 2-azofluorenyl group was prepared and purified specifically by the use of a hapten-specific solid adsorbent. These antibodies, when radiolabeled and injected i.v., were shown to localize specifically in the liver and kidney of rats previously injected with 2-aminofluorene and 2-acetylaminofluorene and also in the liver and kidney of rats fed 2-acetylaminofluorene. The antibodies did not localize in the organs of untreated normal rats or of untreated rats with tumors induced by feeding 2-acetylaminofluorene. The latter rats had not received any carcinogen 0.5–1 year prior to the antibody injection. However, when such tumor-bearing rats were injected with 2-amino- or 2-acetylaminofluorene prior to antibody injection, the antibodies did localize in the apparently healthy portions of liver and kidney, but not in the tumor itself. When rats were injected with 2,7-diacetylaminofluorene, 2-amino-7-acetylaminofluorene, 2,7-diaminofluorene, 2,7-dinitrofluorene, and fluorene, they did not show any localization of the radiolabeled anti-2-azofluorene antibodies above control globulin.

The anti-2-azofluorenyl antibody was shown by radioimmunoelectrophoresis experiments to be directed against the 2-azofluorenyl group since the combination of antibody with antigen was inhibited by the presence of 2-aminofluorene and to a lesser degree by 2-acetylaminofluorene and 2-amino-7-acetylaminofluorene.

The results indicate that some components of the hepatic cell surface are able to combine with fed or injected 2-aminofluorene and 2-acetylaminofluorene and then to fix the antibody in vivo, when the antibody is injected i.v. These components are not present in the tumor.

1 Supported in part by Contract AT(30-1)2651 from the United States Atomic Energy Commission.

2 This work was done during a leave of absence from the Institute for Cancer Research, Osaka University Medical School, Osaka, Japan.

3 A unit of the New York State Department of Health.

Received 7/30/65.





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 Cell Growth & Differentiation
Copyright © 1966 by the American Association for Cancer Research.