Development of a clinically relevant ovarian cancer model incorporating surgical cytoreduction to evaluate treatment of micro-metastatic disease.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
02 2021
Historique:
received: 25 06 2020
accepted: 08 11 2020
pubmed: 25 11 2020
medline: 1 7 2021
entrez: 24 11 2020
Statut: ppublish

Résumé

Mouse models of ovarian cancer commonly transfer large numbers of tumor cells into the peritoneal cavity to establish experimental metastatic disease, which may not adequately model early metastatic spread from a primary tumor site. We hypothesized we could develop an ovarian cancer model that predictably represents micro-metastatic disease. Murine ID8 eLuc-transduced ID8 Mice with primary ovarian tumors established through orthotopic injection develop progressively fatal metastatic ovarian cancer, and benefit from surgical cytoreduction to remove bulky disease. This model enables the analysis of therapeutic regimens designed to target and potentially eradicate established minimal residual disease.

Identifiants

pubmed: 33229044
pii: S0090-8258(20)34117-2
doi: 10.1016/j.ygyno.2020.11.009
pmc: PMC8547140
mid: NIHMS1646135
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

427-437

Subventions

Organisme : NCI NIH HHS
ID : T32 CA009515
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest P.D.G. has patents with, received funding from, and was a scientific consultant to Juno Therapeutics. R.G. has received consulting income from Juno Therapeutics, Takeda, Infotech Soft, Celgene, Merck and has received research support from Janssen Pharmaceuticals and Juno Therapeutics, and declares ownership in CellSpace Biosciences.

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Auteurs

Christopher B Morse (CB)

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Washington, Seattle, WA 98195, United States of America; Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America; Division of Gynecologic Oncology, Allegheny Health Network, West Penn Hospital, Mellon Pavilion, Suite 310, 4815 Liberty Avenue, Pittsburgh, PA 15224, United States of America. Electronic address: Christopher.Morse@ahn.org.

Valentin Voillet (V)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America.

Breanna M Bates (BM)

Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America.

Edison Y Chiu (EY)

Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America.

Nicolas M Garcia (NM)

Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America.

Raphael Gottardo (R)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America.

Philip D Greenberg (PD)

Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America; Divison of Medical Oncology, Department of Medicine, Department of Immunology, University of Washington, Seattle, WA 98195, United States of America. Electronic address: pgreenberg@fredhutch.org.

Kristin G Anderson (KG)

Program in Immunology, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States of America. Electronic address: ande8527@uw.edu.

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