» Articles » PMID: 6584902

O4-ethyldeoxythymidine, but Not O6-ethyldeoxyguanosine, Accumulates in Hepatocyte DNA of Rats Exposed Continuously to Diethylnitrosamine

Overview
Specialty Science
Date 1984 Mar 1
PMID 6584902
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

In previous investigations into the mechanisms responsible for cell specificity in hepatocarcinogenesis, we have demonstrated that O6-methylguanine accumulates in the DNA of nonparenchymal cells (NPC) but is efficiently removed from hepatocellular DNA. O6-Alkylguanine may, therefore, be an important promutagenic lesion responsible for the induction of hepatic angiosarcomas after exposure to methylating agents, but other promutagenic DNA alkylation products--i.e., O4-alkylthymine--may be responsible for the initiation of hepatocellular carcinomas. F-344 male rats were provided drinking water containing diethylnitrosamine (DEN) at 40 ppm for 0, 2, 4, 8, 16, 28, 49, or 77 days, a regimen that selectively causes hepatocellular carcinomas. Hepatocytes and NPC were isolated by using low-speed differential centrifugation. DNA was purified by hydroxyapatite chromatography and hydrolyzed enzymatically, and O4-ethyldeoxythymidine (O4-EtdThd) and O6-ethyldeoxyguanosine (O6-EtdGuo) of hepatocyte and NPC DNA were quantitated by competitive radioimmunoassay using high-affinity monoclonal antibodies. O4-EtdThd accumulated in hepatocyte DNA during the first 28 days of DEN exposure, approximating a steady state at an O4-EtdThd-to-deoxythymidine molar ratio of approximately equal to 1 X 10(-5). This O4-EtdThd concentration was maintained from 28 to 77 days of DEN exposure. In contrast, O6-EtdGuo did not accumulate in hepatocyte DNA, its greatest concentration O6-EtdGuo-to-deoxyguanosine ratio (approximately equal to 3.7 X 10(-7) ) being detected after 2 days of exposure to DEN. O6-EtdGuo concentrations in hepatocyte DNA decreased with duration of exposure to DEN to an O6-EtdGuo-to-deoxyguanosine ratio of less than 2 X 10(-7) from 28 to 77 days. The data indicate that O4-EtdThd disappears from the DNA of hepatocytes less than 1/200th as fast as O6-EtdGuo. DNA from NPC contained approximately half as much O4-EtdThd as hepatocytes did, but greater than or equal to 2.5 times more O6-EtdGuo.

Citing Articles

Metabolic Activation and DNA Interactions of Carcinogenic -Nitrosamines to Which Humans Are Commonly Exposed.

Li Y, Hecht S Int J Mol Sci. 2022; 23(9).

PMID: 35562949 PMC: 9105260. DOI: 10.3390/ijms23094559.


In Vivo and In Vitro Models of Hepatocellular Carcinoma: Current Strategies for Translational Modeling.

Romualdo G, Leroy K, Costa C, Prata G, Vanderborght B, Da Silva T Cancers (Basel). 2021; 13(21).

PMID: 34771745 PMC: 8582701. DOI: 10.3390/cancers13215583.


Recent Studies on DNA Adducts Resulting from Human Exposure to Tobacco Smoke.

Ma B, Stepanov I, Hecht S Toxics. 2019; 7(1).

PMID: 30893918 PMC: 6468371. DOI: 10.3390/toxics7010016.


Understanding the importance of low-molecular weight (ethylene oxide- and propylene oxide-induced) DNA adducts and mutations in risk assessment: Insights from 15 years of research and collaborative discussions.

Pottenger L, Boysen G, Brown K, Cadet J, Fuchs R, Johnson G Environ Mol Mutagen. 2018; 60(2):100-121.

PMID: 30536466 PMC: 6590209. DOI: 10.1002/em.22248.


Mechanism of DNA alkylation-induced transcriptional stalling, lesion bypass, and mutagenesis.

Xu L, Wang W, Wu J, Shin J, Wang P, Unarta I Proc Natl Acad Sci U S A. 2017; 114(34):E7082-E7091.

PMID: 28784758 PMC: 5576830. DOI: 10.1073/pnas.1708748114.


References
1.
Rajewsky M, Dauber W, Frankenberg H . Liver carcinogenesis by diethylnitrosamine in the rat. Science. 1966; 152(3718):83-5. DOI: 10.1126/science.152.3718.83. View

2.
Tomatis L, CEFIS F . The effects of multiple and single administration of dimethylnitrosamine to hamsters. Tumori. 1967; 53(5):447-51. DOI: 10.1177/030089166705300502. View

3.
Rajewsky M . Changes in DNA synthesis and cell proliferation during hepatocarcinogenesis by diethylnitrosamine. Eur J Cancer (1965). 1967; 3(4):335-42. DOI: 10.1016/0014-2964(67)90016-3. View

4.
Druckrey H, PREUSSMANN R, Ivankovic S, Schmahl D . [Organotropic carcinogenic effects of 65 various N-nitroso- compounds on BD rats]. Z Krebsforsch. 1967; 69(2):103-201. View

5.
Rajewsky M . Proliferative parameters of mammalian cell systms and their rôle in tumor growth and carcinogenesis. Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1972; 78(1):12-30. DOI: 10.1007/BF00284309. View