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Open AccessJournal ArticleDOI

The influence of preliminary irritation by acetic acid or croton oil on skin tumour production in mice after a single application of dimethyl-benzathracene, benzopyrene, or dibenzanthracene.

A W Pound
- 01 Sep 1968 - 
- Vol. 22, Iss: 3, pp 533-544
TLDR
It is considered that proliferating epidermal cells are more susceptible to the action of the carcinogens perhaps during replication of DNA.
Abstract
Groups of mice were given a single application of acetic acid to one side of the skin of the back. Other groups were given an application of croton oil to the whole area of the skin of the back, a control group had no application of croton oil. At the same time as, 24 hours, 72 hours, or 9 days after the application of acetic acid or croton oil, the mice were given a single application of one of the carcinogenic hydrocarbons DMBA, BP or DBA, to the whole area of the skin of the back. The number of tumours produced was greater in areas that had the preliminary treatment with acetic acid or croton oil at the same time or 24 hours before the carcinogen. There was a doubtful effect at an interval of 3 days and no effect at 9 days. It is considered that proliferating epidermal cells are more susceptible to the action of the carcinogens perhaps during replication of DNA.

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Citations
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Differentiation of the mammary gland and susceptibility to carcinogenesis

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Book ChapterDOI

The Repair of DNA Modified by Cytotoxic, Mutagenic, and Carcinogenic Chemicals

TL;DR: This chapter discusses some studies on the interaction of various compounds with cellular DNA and the biochemical and biological consequences of these reactions in a variety of cell systems and focuses attention on DNA as the principal target for a number of chemotherapeutically useful cytotoxic agents and for numerous known carcinogens.
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Repeated partial hepatectomy as a promoting stimulus for carcinogenic response of liver to nitrosamines in rats.

TL;DR: The stimulus of repeated partial hepatectomy appears to act as a "promoting agent" for liver carcinogenesis, that is if the single dose of diethylnitrosamine is regarded as an "initiating agent" in the terms of the two-stage hypothesis.
References
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Journal ArticleDOI

Incomplete carcinogens: ethyl carbamate (urethane) as an initiator of skin tumour formation in the mouse.

TL;DR: Incomplete Carcinogens: Ethyl Carbamate (Urethane) as an Initiator of Skin Tumour Formation in the Mouse as mentioned in this paper, which is a complete carcinogen.
Journal ArticleDOI

An experimental analysis of the hair cycle effect in mouse skin carcinogenesis.

TL;DR: In this paper, the authors propose a method to solve the problem of "missing links". But they do not specify how to find the missing links.ImagesFigs. 2-7
Journal ArticleDOI

Studies on co-carcinogenesis. SH-reactors and other substances tested for co-carcinogenic action in mouse skin.

TL;DR: SH-Reactors and other Substances Tested for Co-carcinogenic action in Mouse Skin suggest that SH-reactors act as a ‘spatially aggregating force’ to cause cancer in mice.
Journal ArticleDOI

The influence of some irritant chemicals and scarification on tumour initiation by urethane in mice.

TL;DR: The Influence of Some Irritant Chemicals and Scarification on Tumour Initiation by Urethane in Mice is studied and its effects on tumour initiation are investigated.
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