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A Transplantable Syngeneic Allograft Mouse Model for Nongestational Choriocarcinoma of the Ovary.
Szabova, Ludmila; Karim, Baktiar; Gordon, Melanie; Lu, Lucy; Pate, Nathan; Ohler, Zoe Weaver.
Affiliation
  • Szabova L; 1 Center for Advanced Preclinical Research, Frederick National Laboratory for Cancer Research at the National Cancer Institute-Frederick, Frederick, MD, USA.
  • Karim B; 2 Pathology Histotechnology Laboratory, Laboratory Animal Sciences Program, Frederick National Laboratory for Cancer Research at the National Cancer Institute-Frederick, Frederick, MD, USA.
  • Gordon M; 1 Center for Advanced Preclinical Research, Frederick National Laboratory for Cancer Research at the National Cancer Institute-Frederick, Frederick, MD, USA.
  • Lu L; 3 Center for Advanced Preclinical Research, National Cancer Institute-Frederick, Frederick, MD, USA.
  • Pate N; 1 Center for Advanced Preclinical Research, Frederick National Laboratory for Cancer Research at the National Cancer Institute-Frederick, Frederick, MD, USA.
  • Ohler ZW; 1 Center for Advanced Preclinical Research, Frederick National Laboratory for Cancer Research at the National Cancer Institute-Frederick, Frederick, MD, USA.
Vet Pathol ; 56(3): 399-403, 2019 05.
Article in En | MEDLINE | ID: mdl-30636537
ABSTRACT
Nongestational choriocarcinoma is a rare malignancy in humans with poor prognosis. Naturally occurring choriocarcinoma is also rare in laboratory mice, and no genetic mouse model accurately recapitulates the features of this cancer. Here we report development of a genetically engineered mouse (GEM) model with alterations in Brca2, Trp53, and RB that develops ovarian tumors. Most of the ovarian tumors displayed histological characteristics of nongestational choriocarcinoma of the ovary (NGCO) (47%) with abundant syncytiotrophoblasts and cytotrophoblasts, positive immunolabeling for human chorionic gonadotropin, and positive periodic acid-Schiff reaction. The rest of the ovarian tumors were serous epithelial ovarian carcinoma (SEOC) (26%) or mixed tumors consisting of NGCO and SEOC (26%). We further established syngeneic orthotopic mouse models for NGCO by in vivo passaging of GEM tumors. These metastatic models provide a platform for evaluating new treatment strategies in preclinical studies aimed at improving outcomes in choriocarcinoma patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Choriocarcinoma, Non-gestational / Neoplasm Transplantation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Vet Pathol Year: 2019 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ovarian Neoplasms / Choriocarcinoma, Non-gestational / Neoplasm Transplantation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Vet Pathol Year: 2019 Type: Article Affiliation country: United States