Cancer Research CTRC-AACR San Antonio Breast Cancer Symposium
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

[Cancer Research 28, 2565-2567, December 1, 1968]
© 1968 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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sunderman, F. W.
Right arrow Articles by Esfahani, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sunderman, F. W., Jr.
Right arrow Articles by Esfahani, M.

Nickel Carbonyl Inhibition of RNA Polymerase Activity in Hepatic Nuclei1

F. William Sunderman, Jr.2 and Mojtaba Esfahani3

Pathology Department, University of Florida College of Medicine, Gainesville, Florida 32601

Nickel carbonyl, a metallic carcinogen, was found to be an inhibitor of DNA-dependent RNA polymerase activity in hepatic nuclei. The mean RNA polymerase activity in hepatic nuclei of control rats was 2.67 (S.D. ± 0.46) units. In rats which received an intravenous injection of nickel carbonyl (2.2 mg Ni/100 gm) 24 hr before sacrifice, the mean RNA polymerase activity was 1.07 ± 0.53 units (P vs untreated controls less double equals 0.01). Nickel carbonyl also inhibited. hepatic RNA polymerase activity in rats which received phenobarbital (10 mg/100 gm, i.p.) 20 hr before sacrifice. Phenobarbital administration increased the mean RNA polymerase activity in hepatic nuclei to 3.48 ± 0.54 units (P vs untreated controls less double equals 0.01). In rats which received nickel carbonyl 24 hr before sacrifice and phenobarbital 20 hr before sacrifice, the mean RNA polymerase activity was 1.54 ± 0.88 units (P vs phenobarbital-treated controls less double equals 0.01).

1 This investigation was supported by U.S. Atomic Energy Commission Grant No. AT-(40-1)-3461, American Cancer Society Grant No. E-374B, and USPHS research Grant No. CA-08783-02 from the National Cancer Institute.

2 Present address: Department of Laboratory Medicine, University of Connecticut School of Medicine, 2 Holcomb St., Hartford, Connecticut, 06112.

3 Present address: Department of Biochemistry, Duke University School of Medicine, Durham, North Carolina, 27706.

Received 5/16/68. Accepted 8/28/68.




This article has been cited by other articles:


Home page
ScienceHome page
F. Sunderman Jr, P. Allpass, J. Mitchell, R. Baselt, and D. Albert
Eye malformations in rats: induction by prenatal exposure to nickel carbonyl
Science, February 9, 1979; 203(4380): 550 - 553.
[Abstract] [PDF]




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 © 1968 by the American Association for Cancer Research.