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Published in: Breast Cancer Research and Treatment 3/2010

01-08-2010 | Preclinical study

Demonstration of anti-tumor activity of oncolytic measles virus strains in a malignant pleural effusion breast cancer model

Authors: Ianko D. Iankov, Pavlos Msaouel, Cory Allen, Mark J. Federspiel, Peggy A. Bulur, Allan B. Dietz, Dennis Gastineau, Yasuhiro Ikeda, James N. Ingle, Stephen J. Russell, Evanthia Galanis

Published in: Breast Cancer Research and Treatment | Issue 3/2010

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Abstract

Breast cancer is the second leading cause of malignant effusions in cancer patients. Pleural effusion indicates incurable disease with limited palliative treatment options and poor outcome. Here, we demonstrate the therapeutic efficacy of measles virus (MV) vaccine strain derivative against malignant pleural effusion in an MDA-MB-231 xenograft model of advanced breast cancer. Both systemic intravenous (i.v.) and intrapleural (t.t.) administered virus caused massive infection and syncytia formation in the pleural tumor deposits. Intrapleural administration of 1.5 × 106 plaque-forming units (PFU) total dose of MV significantly improved median survival by approximately 80% compared to the control animal group. Furthermore, we tested human dendritic cells as carriers for delivery of oncolytic MV infection to breast cancer pleural metastases. Carrier-delivered MV infection prevented accumulation of the pleural exudate and also significantly improved the survival of the treated mice. This is the first demonstration of the therapeutic potential of oncolytic virotherapy against malignant pleural effusions in a pre-clinical model of advanced breast cancer.
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Metadata
Title
Demonstration of anti-tumor activity of oncolytic measles virus strains in a malignant pleural effusion breast cancer model
Authors
Ianko D. Iankov
Pavlos Msaouel
Cory Allen
Mark J. Federspiel
Peggy A. Bulur
Allan B. Dietz
Dennis Gastineau
Yasuhiro Ikeda
James N. Ingle
Stephen J. Russell
Evanthia Galanis
Publication date
01-08-2010
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2010
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-009-0602-z

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