Literature DB >> 179560

Comparison of tumour susceptibility among various organs of foetal, young and adult ICR/Jcl mice.

T Nomura.   

Abstract

Urethane was found to be uniformly distributed in all the major organs of foetal, young and adult ICR/Jcl mice and then to disappear rapidly as measured by the incorporation of urethane-carbonyl-14C, thus permitting the accurate comparison of tumour susceptibility of cells in various organs of mice at different ages. Lung tumour frequency (tumours/lung) was significantly higher in mice treated with urethane when young (21 days old) and adult (63 days old) than in those treated in utero (Days 11-19 of gestation). When relative sensitivity of a lung cell was calculated as the ratio of average number of tumours per lung per mg of lung at the time of treatment, however, a lung cell of the foetus was more sensitive to urethane than that of the young and adult. Hepatomata were induced significantly only when male foetuses and neonates were exposed to urethane. The offspring exposed to urethane on Days 11-16, however, developed hepatomata in lower incidence than those exposed on Days 14-19, whereas the previous investigation by the author revealed that Days 11-13 correspond to the stage most sensitive to hepatocarcinogenesis. This contradiction was due to the occurrence of testicular hypogenesis (chemical castration) in all offspring of the former group. Differentiating female gonad and rapidly proliferating blood vessels of the placenta and deciduum were also sensitive to tumour induction by urethane. Thus, high tumour susceptibility of rapidly proliferating and undifferentiated cells suggests that some initiating events in the process of carcinogenesis may occur during or after DNA replication. Leukaemia induction in the young mice, but not in the foetus, remains to be elucidated.

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Year:  1976        PMID: 179560      PMCID: PMC2024959          DOI: 10.1038/bjc.1976.83

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  27 in total

1.  Distribution of C14-labeled urethans in tissues of the mouse and subcellular localization in lung and liver.

Authors:  I BERENBLUM; N HARAN-GHERA; R WINNICK; T WINNICK
Journal:  Cancer Res       Date:  1958-02       Impact factor: 12.701

2.  Normal and pathologic anatomy of the reticular tissue in laboratory mice, with a classification and discussion of neoplasms.

Authors:  T B DUNN
Journal:  J Natl Cancer Inst       Date:  1954-06       Impact factor: 13.506

3.  Hormonal aspects of experimental tumorigenesis.

Authors:  W U GARDNER
Journal:  Adv Cancer Res       Date:  1953       Impact factor: 6.242

4.  Sensitivity of a lung cell in the developing mouse embryo to tumor induction by urethan.

Authors:  T Nomura
Journal:  Cancer Res       Date:  1974-12       Impact factor: 12.701

5.  Long retention of urethan transferred into newborn mice transplacentally, as a possible cause of high carcinogenesis.

Authors:  T Nomura; H Takebe; E Okamoto
Journal:  Gan       Date:  1973-02

6.  [Dynamics of the transplacental penetration of 7,12-dimethylbenz(a)anthracene (DMBA) in mice].

Authors:  I A Shendrikova; M N Ivanov-Golitsyn; V N Anisimov; A Ia Likhachev
Journal:  Vopr Onkol       Date:  1973-05

7.  An analysis of the changing urethan response of the developing mouse embryo in relation to mortality, malformation, and neoplasm.

Authors:  T Nomura
Journal:  Cancer Res       Date:  1974-09       Impact factor: 12.701

8.  Transplacental carcinogenic effect of 3-methylcholanthrene in mice and its quantitation in fetal tissues.

Authors:  L Tomatis; V Turusov; D Guibbert; B Duperray; C Malaveille; H Pacheco
Journal:  J Natl Cancer Inst       Date:  1971-09       Impact factor: 13.506

9.  The catabolism of urethan in young mice of varying age and strain, and in x-irradiated mice, in relation to urethan carcinogenesis.

Authors:  G Cividalli; S S Mirvish; I Berenblum
Journal:  Cancer Res       Date:  1965-07       Impact factor: 12.701

10.  Progression of pulmonary tumor in mice. 1. Histological studies of primary and transplanted pulmonary tumors.

Authors:  K Kimura
Journal:  Acta Pathol Jpn       Date:  1971-02
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  3 in total

1.  Comparison of carcinogenic potency across life stages: implications for the assessment of transplacental cancer risk.

Authors:  R Dzubow; C Fields; G Ginsberg; M Sandy; M Mabson; B Foos
Journal:  J Toxicol Environ Health A       Date:  2019-08-11

2.  Age-related differences in susceptibility to carcinogenesis. II. Approaches for application and uncertainty analyses for individual genetically acting carcinogens.

Authors:  Dale Hattis; Robert Goble; Margaret Chu
Journal:  Environ Health Perspect       Date:  2005-04       Impact factor: 9.031

3.  Age-related differences in susceptibility to carcinogenesis: a quantitative analysis of empirical animal bioassay data.

Authors:  Dale Hattis; Robert Goble; Abel Russ; Margaret Chu; Jen Ericson
Journal:  Environ Health Perspect       Date:  2004-08       Impact factor: 9.031

  3 in total

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