Literature DB >> 2501249

Advantages and limitations of stereological estimation of placental glutathione S-transferase-positive rat liver cell foci by computerized three-dimensional reconstruction.

K Imaida1, M Tatematsu, T Kato, H Tsuda, N Ito.   

Abstract

The applicability to a medium-term bioassay for liver carcinogens of mathematical formulae for the calculation of numbers of foci per volume was examined in F344 rats. Two weeks after initiation with diethylnitrosamine, animals were given test compounds for 6 weeks, partial hepatectomy being performed at week 3. At week 8, the rats were killed, the livers removed and stained immunohistochemically for assessment of glutathione S-transferase P form (GST-P)-positive foci development. Numbers and areas of lesions were measured two-dimensionally using a color image analyzer, and the Enzmann and Campbell formulae for estimation of number and volume per cm3 were applied to the results. In addition, three-dimensional reconstruction of individual foci was performed using up to 150 GST-P stained foci, with the aid of a computerized graphic system. Both two- and three-dimensionally expressed quantitative results were found to adequately demonstrate the modifying potential of test chemicals on hepatocarcinogenesis. The three-dimensional approach was only more accurate if most of the foci were small and the liver was enlarged by compound treatment. Stereological reconstruction revealed that the shape of GST-P-positive foci, especially if relatively large, is not always spherical but that many demonstrate irregular branching forms, so that the assumptions behind stereological estimation are not met. The results therefore show that care must be taken in applying mathematical formulae for the calculation of three-dimensional data.

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Year:  1989        PMID: 2501249      PMCID: PMC5917743          DOI: 10.1111/j.1349-7006.1989.tb02314.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


  22 in total

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Authors:  H Yaegashi; T Takahashi; M Kawasaki
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2.  Simple elementary method for the quantification of focal liver lesions induced by carcinogens.

Authors:  H Enzmann; L Edler; P Bannasch
Journal:  Carcinogenesis       Date:  1987-02       Impact factor: 4.944

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Authors:  J J Capowski
Journal:  Comput Biomed Res       Date:  1977-12

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Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

Review 5.  Three-dimensional microstructure of gastrointestinal tumors. Gland pattern and its diagnostic significance.

Authors:  T Takahashi; N Iwama
Journal:  Pathol Annu       Date:  1985

6.  Application of quantitative stereology to the evaluation of enzyme-altered foci in rat liver.

Authors:  H A Campbell; H C Pitot; V R Potter; B A Laishes
Journal:  Cancer Res       Date:  1982-02       Impact factor: 12.701

7.  Placental glutathione S-transferase (GST-P) as a new marker for hepatocarcinogenesis: in vivo short-term screening for hepatocarcinogens.

Authors:  M Tatematsu; H Tsuda; T Shirai; T Masui; N Ito
Journal:  Toxicol Pathol       Date:  1987       Impact factor: 1.902

8.  Quantitative stereological evaluation of four histochemical markers of altered foci in multistage hepatocarcinogenesis in the rat.

Authors:  S Hendrich; H A Campbell; H C Pitot
Journal:  Carcinogenesis       Date:  1987-09       Impact factor: 4.944

9.  Topological analysis of the morphogenesis of liver cirrhosis.

Authors:  T Takahashi
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1978-03-10

10.  Quantitative evaluation of the promotion by 2,3,7,8-tetrachlorodibenzo-p-dioxin of hepatocarcinogenesis from diethylnitrosamine.

Authors:  H C Pitot; T Goldsworthy; H A Campbell; A Poland
Journal:  Cancer Res       Date:  1980-10       Impact factor: 12.701

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  5 in total

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Journal:  J Mol Histol       Date:  2008-12-04       Impact factor: 2.611

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Authors:  Anna Kakehashi; Ayumi Kato; Naomi Ishii; Min Wei; Keiichirou Morimura; Shoji Fukushima; Hideki Wanibuchi
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3.  A 2-year dose-response study of lesion sequences during hepatocellular carcinogenesis in the male B6C3F(1) mouse given the drinking water chemical dichloroacetic acid.

Authors:  Julia H Carter; Harry W Carter; James A Deddens; Bernadette M Hurst; Michael H George; Anthony B DeAngelo
Journal:  Environ Health Perspect       Date:  2003-01       Impact factor: 9.031

4.  Reversibility of carcinogen-induced rat forestomach basal cell hyperplasia is due to squamous cell differentiation.

Authors:  K Ogawa; T Hoshiya; T Kato; T Shirai; M Tatematsu
Journal:  Jpn J Cancer Res       Date:  1992-07

5.  Three-dimensional analysis of glutathione S-transferase placental form-positive lesion development in early stages of rat hepatocarcinogenesis.

Authors:  T Kato; K Imaida; K Ogawa; R Hesegawa; T Shirai; M Tatematsu
Journal:  Jpn J Cancer Res       Date:  1993-12
  5 in total

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