Mesenchymal stem cells as a vehicle for targeted delivery of CRAds to lung metastases of breast carcinoma
Autor: | Amanda S Moon, Louise T. Chow, David T. Curiel, Mariam A. Stoff-Khalili, Peter Dall, Larissa Pereboeva, Rodney P. Rocconi, Gene P. Siegal, J. Michael Mathis, Hans Georg Bender, N. Sanjib Banerjee, Zeng B. Zhu, Alexander Stoff, Angel A. Rivera, Joanne T. Douglas, Alexandra P. Hess, Maaike Everts, T. Michael Numnum |
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Rok vydání: | 2007 |
Předmět: |
Oncology
Receptors CXCR4 Cancer Research medicine.medical_specialty Lung Neoplasms Genetic Vectors Transplantation Heterologous Breast Neoplasms Mice SCID Adenoviridae Metastasis Mice Breast cancer Internal medicine Tumor Cells Cultured Animals Humans Medicine Virotherapy Promoter Regions Genetic business.industry Mesenchymal stem cell Cancer Mesenchymal Stem Cells Genetic Therapy equipment and supplies medicine.disease Metastatic breast cancer Survival Rate Transplantation Female Stem cell business |
Zdroj: | Breast Cancer Research and Treatment. 105:157-167 |
ISSN: | 1573-7217 0167-6806 |
DOI: | 10.1007/s10549-006-9449-8 |
Popis: | Alternative and complementary therapeutic strategies need to be developed for metastatic breast cancer. Virotherapy is a novel therapeutic approach for the treatment of cancer in which the replicating virus itself is the anticancer agent. However, the success of virotherapy has been limited due to inefficient virus delivery to the tumor site. The present study addresses the utility of human mesenchymal stem cells (hMSCs) as intermediate carriers for conditionally replicating adenoviruses (CRAds) to target metastatic breast cancer in vivo. HMSC were transduced with CRAds. We used a SCID mouse xenograft model to examine the effects of systemically injected CRAd loaded hMSC or CRAd alone on the growth of MDA-MB-231 derived pulmonary metastases (experimental metastases model) in vivo and on overall survival. Intravenous injection of CRAd loaded hMSCs into mice with established MDA-MB-231 pulmonary metastatic disease homed to the tumor site and led to extended mouse survival compared to mice treated with CRAd alone. Injected hMSCs transduced with CRAds suppressed the growth of pulmonary metastases, presumably through viral amplification in the hMSCs. Thus, hMSCs may be an effective platform for the targeted delivery of CRAds to distant cancer sites such as metastatic breast cancer. |
Databáze: | OpenAIRE |
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