Cargando…

Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry

The number of silver‐stained nucleolar proteins (AgNOR) was counted in preneoplastic and neoplastic rat liver lesions induced by N‐2‐fluorenylacetamide (FAA) and was compared with that of bromodeoxyuridine (BrdU)‐incorporating cells detected immunohistochemically using monoclonal antibody against Br...

Descripción completa

Detalles Bibliográficos
Autores principales: Tanaka, Takuji, Takeuchi, Toshimi, Nishikawa, Akiyoshi, Takami, Tsuyoshi, Mori, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917911/
https://www.ncbi.nlm.nih.gov/pubmed/2514166
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02257.x
_version_ 1783317317157912576
author Tanaka, Takuji
Takeuchi, Toshimi
Nishikawa, Akiyoshi
Takami, Tsuyoshi
Mori, Hideki
author_facet Tanaka, Takuji
Takeuchi, Toshimi
Nishikawa, Akiyoshi
Takami, Tsuyoshi
Mori, Hideki
author_sort Tanaka, Takuji
collection PubMed
description The number of silver‐stained nucleolar proteins (AgNOR) was counted in preneoplastic and neoplastic rat liver lesions induced by N‐2‐fluorenylacetamide (FAA) and was compared with that of bromodeoxyuridine (BrdU)‐incorporating cells detected immunohistochemically using monoclonal antibody against BrdU. Male ACI/N rats were given diet containing 200 ppm FAA for 12, 16 or 20 weeks to induce hepatocellular foci and tumors. The mean numbers of AgNOR stained by a one‐step silver colloid method and BrdU‐labeling indices in various liver cell lesions were as follows: nontreated liver (n = 20), 1.20 and 0.08; nonlesional areas (n=20), 1.33 and 0.13; altered liver cell foci (n = 80), 2.04 and 4.05 [eosinophilic cell type (n = 20), 1.78 and 1.82; clear cell type (n=20), 1.45 and 1.77; basophilic cell type (n=20), 1.99 and 4.58; hyperbasophilic cell type (n=20), 2.94 and 8.02]; neoplastic nodules (n = 10), 3.11 and 2.99; hepatocellular carcinomas (n = 10), 7.22 and 8.29. Thus, the mean number of AgNOR and the value of BrdU‐labeling index were well correlated and both values showed a stepwise increase from normal liver cells to liver cell carcinoma, although some scatter was present. These data suggest that mean number of AgNOR may reflect the cellular kinetics in rat hepatocarcinogenesis, and the one‐step silver colloid method for demonstration of AgNOR may therefore be a simple and useful staining to examine the proliferative nature of cells.
format Online
Article
Text
id pubmed-5917911
institution National Center for Biotechnology Information
language English
publishDate 1989
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-59179112018-05-11 Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry Tanaka, Takuji Takeuchi, Toshimi Nishikawa, Akiyoshi Takami, Tsuyoshi Mori, Hideki Jpn J Cancer Res Article The number of silver‐stained nucleolar proteins (AgNOR) was counted in preneoplastic and neoplastic rat liver lesions induced by N‐2‐fluorenylacetamide (FAA) and was compared with that of bromodeoxyuridine (BrdU)‐incorporating cells detected immunohistochemically using monoclonal antibody against BrdU. Male ACI/N rats were given diet containing 200 ppm FAA for 12, 16 or 20 weeks to induce hepatocellular foci and tumors. The mean numbers of AgNOR stained by a one‐step silver colloid method and BrdU‐labeling indices in various liver cell lesions were as follows: nontreated liver (n = 20), 1.20 and 0.08; nonlesional areas (n=20), 1.33 and 0.13; altered liver cell foci (n = 80), 2.04 and 4.05 [eosinophilic cell type (n = 20), 1.78 and 1.82; clear cell type (n=20), 1.45 and 1.77; basophilic cell type (n=20), 1.99 and 4.58; hyperbasophilic cell type (n=20), 2.94 and 8.02]; neoplastic nodules (n = 10), 3.11 and 2.99; hepatocellular carcinomas (n = 10), 7.22 and 8.29. Thus, the mean number of AgNOR and the value of BrdU‐labeling index were well correlated and both values showed a stepwise increase from normal liver cells to liver cell carcinoma, although some scatter was present. These data suggest that mean number of AgNOR may reflect the cellular kinetics in rat hepatocarcinogenesis, and the one‐step silver colloid method for demonstration of AgNOR may therefore be a simple and useful staining to examine the proliferative nature of cells. Blackwell Publishing Ltd 1989-11 /pmc/articles/PMC5917911/ /pubmed/2514166 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02257.x Text en
spellingShingle Article
Tanaka, Takuji
Takeuchi, Toshimi
Nishikawa, Akiyoshi
Takami, Tsuyoshi
Mori, Hideki
Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title_full Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title_fullStr Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title_full_unstemmed Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title_short Nucleolar Organizer Regions in Hepatocarcinogenesis Induced by N‐2‐Fluorenylacetamide in Rats: Comparison with Bromodeoxyuridine Immunohistochemistry
title_sort nucleolar organizer regions in hepatocarcinogenesis induced by n‐2‐fluorenylacetamide in rats: comparison with bromodeoxyuridine immunohistochemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917911/
https://www.ncbi.nlm.nih.gov/pubmed/2514166
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02257.x
work_keys_str_mv AT tanakatakuji nucleolarorganizerregionsinhepatocarcinogenesisinducedbyn2fluorenylacetamideinratscomparisonwithbromodeoxyuridineimmunohistochemistry
AT takeuchitoshimi nucleolarorganizerregionsinhepatocarcinogenesisinducedbyn2fluorenylacetamideinratscomparisonwithbromodeoxyuridineimmunohistochemistry
AT nishikawaakiyoshi nucleolarorganizerregionsinhepatocarcinogenesisinducedbyn2fluorenylacetamideinratscomparisonwithbromodeoxyuridineimmunohistochemistry
AT takamitsuyoshi nucleolarorganizerregionsinhepatocarcinogenesisinducedbyn2fluorenylacetamideinratscomparisonwithbromodeoxyuridineimmunohistochemistry
AT morihideki nucleolarorganizerregionsinhepatocarcinogenesisinducedbyn2fluorenylacetamideinratscomparisonwithbromodeoxyuridineimmunohistochemistry