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Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos

Parthenogenesis has been suggested to be tightly coupled with development of ovarian teratomas. Indeed, ovarian tumors developed in c‐mos‐delieicnt female mice, which are characterized by the parthenogenetic activation of oocytes. The tumors appeared at a frequency of 30% between 4 and 8 months of a...

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Detalles Bibliográficos
Autores principales: Furuta, Yasuhide, Shigetani, Yasuyo, Takeda, Naoki, Iwasaki, Kuniko, Ikawa, Yoji, Aizawa, Shinichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920872/
https://www.ncbi.nlm.nih.gov/pubmed/7622418
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02432.x
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author Furuta, Yasuhide
Shigetani, Yasuyo
Takeda, Naoki
Iwasaki, Kuniko
Ikawa, Yoji
Aizawa, Shinichi
author_facet Furuta, Yasuhide
Shigetani, Yasuyo
Takeda, Naoki
Iwasaki, Kuniko
Ikawa, Yoji
Aizawa, Shinichi
author_sort Furuta, Yasuhide
collection PubMed
description Parthenogenesis has been suggested to be tightly coupled with development of ovarian teratomas. Indeed, ovarian tumors developed in c‐mos‐delieicnt female mice, which are characterized by the parthenogenetic activation of oocytes. The tumors appeared at a frequency of 30% between 4 and 8 months of age, and did not develop in younger or older mice. Most of the tumors were benign and consisted of multi‐focal cysts most notably with mature ectodermal components, but also with mesodermal and endodermal components. One among 17 tumors observed consisted of extraembryonic tissues alone, and two bore malignant components with metastasis to peritoneal organs. The results strongly suggest the involvement of c‐mos mutations in human germ cell tumors.
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spelling pubmed-59208722018-05-11 Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos Furuta, Yasuhide Shigetani, Yasuyo Takeda, Naoki Iwasaki, Kuniko Ikawa, Yoji Aizawa, Shinichi Jpn J Cancer Res Article Parthenogenesis has been suggested to be tightly coupled with development of ovarian teratomas. Indeed, ovarian tumors developed in c‐mos‐delieicnt female mice, which are characterized by the parthenogenetic activation of oocytes. The tumors appeared at a frequency of 30% between 4 and 8 months of age, and did not develop in younger or older mice. Most of the tumors were benign and consisted of multi‐focal cysts most notably with mature ectodermal components, but also with mesodermal and endodermal components. One among 17 tumors observed consisted of extraembryonic tissues alone, and two bore malignant components with metastasis to peritoneal organs. The results strongly suggest the involvement of c‐mos mutations in human germ cell tumors. Blackwell Publishing Ltd 1995-06 /pmc/articles/PMC5920872/ /pubmed/7622418 http://dx.doi.org/10.1111/j.1349-7006.1995.tb02432.x Text en
spellingShingle Article
Furuta, Yasuhide
Shigetani, Yasuyo
Takeda, Naoki
Iwasaki, Kuniko
Ikawa, Yoji
Aizawa, Shinichi
Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title_full Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title_fullStr Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title_full_unstemmed Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title_short Ovarian Teratomas in Mice Lacking the Protooncogene c‐mos
title_sort ovarian teratomas in mice lacking the protooncogene c‐mos
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920872/
https://www.ncbi.nlm.nih.gov/pubmed/7622418
http://dx.doi.org/10.1111/j.1349-7006.1995.tb02432.x
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