Genetic control of susceptibility to 3-methylcholanthrene-induced subcutaneous sarcomas
✍ Scribed by Richard E. Kouri; Harry Ratrie III; Carrie E. Whitmire
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- French
- Weight
- 534 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Using a genetic system in which aryl hydrocarbon hydroxylase (AHH) inducibility segregates, it was observed that inducible mice are approximately 12 times more sensitive to 3‐methylcholanthrene‐induced tumorigenesis than their non‐inducible littermates. The type of parental cross (maternal influence) plays no role in this sensitivity. Hostregulated expression of the group‐specific (gs) antigen of type‐C RNA viruses, although also segregating in this genetic system, does not seem to play a major role in this enhanced susceptibility to 3‐methylcholanthrene carcinogenesis. Results are discussed with the view that the enhanced sensitivity of the AHH‐inducible animals probably results from rapid and efficient metabolism of the chemical to its ultimate carcinogenic form.
📜 SIMILAR VOLUMES
The responsiveness of the hepatic supernatant NAD+-dependent aldehyde dehydrogenase with a high Km value (high Km-AldDH) to phenobarbital (PB) and 3-methylcholanthrene (3-MC) treatment was studied in male rats of three strains; Wistar, Long-Evans, and Sprague-Dawley. A remarkable strain difference i
## Objective: To study the genes in the mouse background which predispose to the development of collagen-induced arthritis (cia). ## Methods: T cell receptor beta transgenic (tcrbetal) mice that have a t cell repertoire that predisposes to the development of cia were used. classic genetic studies
The response of BALBl3T3 clone A31-1-1 cells to chemically induced morphological transformation was evaluated using 3-methylcholanthrene (MCA). Stock cultures were initiated from cryopreserved cells, grown in T25 flasks containing 5 ml of medium, and replated at subconfluency. Serially transferred c
To assess genetic factors determining sensitivity to streptozotocin-induced diabetes in inbred strains of mice, a genetic analysis of streptozotocin-sensitive C57BL/6J and streptozotocin-resistant C3H/HeJ mice was performed. One week after a single dose of streptozotocin (200 mg/kg body weight), dif