Abstract |
Nongestational ovarian choriocarcinoma (NGCO) is a tumor of germ cell origin seldom described in nonhuman species. Few spontaneous cases are reported in macaques and mice, with the B6C3F1 strain overrepresented. This report describes 2 cases of ovarian choriocarcinoma in nulliparous female mice with conditional loss of Trp53 under the Tie2 promoter. The mouse line was maintained on a mixed genetic background including Crl: CD1(ICR) and 129X1/SvJ strains. In both cases, affected ovary was partially replaced by blood-filled lacunae lined by neoplastic trophoblast-like giant cells. Immunohistochemically, neoplastic cells expressed folate- binding protein and prolactin and were invariably negative for p53. To the authors' knowledge, this is the first report characterizing this entity in a genetically engineered mouse (GEM) line. Considering that germ cells (the cell population from which NGCO originates) constitutively express Tie2 receptor, it can be speculated that Tie2-driven deletion of Trp53 may have played a role in the development of these tumors.
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Authors | V Castiglioni, M Farhang Ghahremani, S Goossens, M De Maglie, M Ardizzone, J J Haigh, E Radaelli |
Journal | Veterinary pathology
(Vet Pathol)
Vol. 52
Issue 4
Pg. 752-6
(Jul 2015)
ISSN: 1544-2217 [Electronic] United States |
PMID | 25253064
(Publication Type: Case Reports, Journal Article)
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Copyright | © The Author(s) 2014. |
Chemical References |
- Tumor Suppressor Protein p53
- Receptor, TIE-2
- Tek protein, mouse
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Topics |
- Animals
- Choriocarcinoma
(pathology, veterinary)
- Female
- Immunohistochemistry
(veterinary)
- Mice
- Mice, Inbred ICR
- Mice, Transgenic
- Neoplasms, Germ Cell and Embryonal
(pathology, veterinary)
- Ovarian Neoplasms
(pathology, veterinary)
- Pregnancy
- Receptor, TIE-2
(genetics)
- Tumor Suppressor Protein p53
(genetics)
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