Cargando…

Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol

In an attempt to induce prostatic adenocarcinoma at higher incidence in a shorter period, we administered diet containing 0.75 ppm of ethinyl estradiol (EE) for three weeks to ACI/Seg rats, which are predisposed to develop a high incidence of microscopic adenocarcinoma of the prostate at higher age....

Descripción completa

Detalles Bibliográficos
Autores principales: Takai, Kazuhiro, Kakizoe, Tadao, Tanaka, Yoshinori, Tobisu, Ken‐ichi, Aso, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918399/
https://www.ncbi.nlm.nih.gov/pubmed/1708755
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01844.x
_version_ 1783317411765682176
author Takai, Kazuhiro
Kakizoe, Tadao
Tanaka, Yoshinori
Tobisu, Ken‐ichi
Aso, Yoshio
author_facet Takai, Kazuhiro
Kakizoe, Tadao
Tanaka, Yoshinori
Tobisu, Ken‐ichi
Aso, Yoshio
author_sort Takai, Kazuhiro
collection PubMed
description In an attempt to induce prostatic adenocarcinoma at higher incidence in a shorter period, we administered diet containing 0.75 ppm of ethinyl estradiol (EE) for three weeks to ACI/Seg rats, which are predisposed to develop a high incidence of microscopic adenocarcinoma of the prostate at higher age. Then, feeding was changed to basal diet and a single subcutaneous injection of 50 mg/kg body weight of 3,2′‐dimethyl‐4‐aminobiphenyl (DMAB) was given two days after the change. We repeated this schedule 10 times. The rats were killed in week 60 of the experiment and subjected to routine autopsy. The average body weight of rats in group 1 given EE and DMAB was lower than that of control rats in group 2. The incidence of adenocarcinoma was not significantly different in the two groups, i.e. 6/74 (8.1%) in group 1 and 2/54 (3.7%) in group 2. The lesions were all microscopic. The incidence of atypical hyperplasia was significantly higher in group 1 at 17 of 74 rats (23.0%) whereas in group 2, it was only 2 of 54 rats (3.7%). Simple hyperplasia was also observed in 25 of 74 rats (33.8%) in group 1, which was significantly higher than that in group 2, where six of 54 rats (11.1%) had this lesion. The reduced growth of animals due to treatments with EE and DMAB probably suppressed the development of prostate cancer in this experiment. Further studies are needed to develop an appropriate model to induce prostate carcinoma at higher incidence in a shorter period.
format Online
Article
Text
id pubmed-5918399
institution National Center for Biotechnology Information
language English
publishDate 1991
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-59183992018-05-11 Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol Takai, Kazuhiro Kakizoe, Tadao Tanaka, Yoshinori Tobisu, Ken‐ichi Aso, Yoshio Jpn J Cancer Res Article In an attempt to induce prostatic adenocarcinoma at higher incidence in a shorter period, we administered diet containing 0.75 ppm of ethinyl estradiol (EE) for three weeks to ACI/Seg rats, which are predisposed to develop a high incidence of microscopic adenocarcinoma of the prostate at higher age. Then, feeding was changed to basal diet and a single subcutaneous injection of 50 mg/kg body weight of 3,2′‐dimethyl‐4‐aminobiphenyl (DMAB) was given two days after the change. We repeated this schedule 10 times. The rats were killed in week 60 of the experiment and subjected to routine autopsy. The average body weight of rats in group 1 given EE and DMAB was lower than that of control rats in group 2. The incidence of adenocarcinoma was not significantly different in the two groups, i.e. 6/74 (8.1%) in group 1 and 2/54 (3.7%) in group 2. The lesions were all microscopic. The incidence of atypical hyperplasia was significantly higher in group 1 at 17 of 74 rats (23.0%) whereas in group 2, it was only 2 of 54 rats (3.7%). Simple hyperplasia was also observed in 25 of 74 rats (33.8%) in group 1, which was significantly higher than that in group 2, where six of 54 rats (11.1%) had this lesion. The reduced growth of animals due to treatments with EE and DMAB probably suppressed the development of prostate cancer in this experiment. Further studies are needed to develop an appropriate model to induce prostate carcinoma at higher incidence in a shorter period. Blackwell Publishing Ltd 1991-03 /pmc/articles/PMC5918399/ /pubmed/1708755 http://dx.doi.org/10.1111/j.1349-7006.1991.tb01844.x Text en
spellingShingle Article
Takai, Kazuhiro
Kakizoe, Tadao
Tanaka, Yoshinori
Tobisu, Ken‐ichi
Aso, Yoshio
Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title_full Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title_fullStr Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title_full_unstemmed Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title_short Trial to Induce Prostatic Cancer in ACI/Seg Rats Treated with a Combination of 3,2′‐Dimethyl‐4‐aminobiphenyl and Ethinyl Estradiol
title_sort trial to induce prostatic cancer in aci/seg rats treated with a combination of 3,2′‐dimethyl‐4‐aminobiphenyl and ethinyl estradiol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918399/
https://www.ncbi.nlm.nih.gov/pubmed/1708755
http://dx.doi.org/10.1111/j.1349-7006.1991.tb01844.x
work_keys_str_mv AT takaikazuhiro trialtoinduceprostaticcancerinacisegratstreatedwithacombinationof32dimethyl4aminobiphenylandethinylestradiol
AT kakizoetadao trialtoinduceprostaticcancerinacisegratstreatedwithacombinationof32dimethyl4aminobiphenylandethinylestradiol
AT tanakayoshinori trialtoinduceprostaticcancerinacisegratstreatedwithacombinationof32dimethyl4aminobiphenylandethinylestradiol
AT tobisukenichi trialtoinduceprostaticcancerinacisegratstreatedwithacombinationof32dimethyl4aminobiphenylandethinylestradiol
AT asoyoshio trialtoinduceprostaticcancerinacisegratstreatedwithacombinationof32dimethyl4aminobiphenylandethinylestradiol