Effective treatment of mouse metastatic prostate cancer by low electric field enhanced chemotherapy

BACKGROUND We developed a new anti‐cancer treatment, which is a combination of chemotherapeutic agents and low electric field. In the present study we investigated its efficacy against prostate metastatic transgenic adenocarcinoma of mice (TRAMP). METHODS Mice with 5, 10, and 13 mm in diameter intra...

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Published inThe Prostate Vol. 66; no. 15; pp. 1620 - 1630
Main Authors Plotnikov, Alexander, Niego, Be'eri, Ophir, Rachel, Korenstein, Rafi, Keisari, Yona
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.11.2006
Wiley-Liss
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Summary:BACKGROUND We developed a new anti‐cancer treatment, which is a combination of chemotherapeutic agents and low electric field. In the present study we investigated its efficacy against prostate metastatic transgenic adenocarcinoma of mice (TRAMP). METHODS Mice with 5, 10, and 13 mm in diameter intracutaneous tumors received Low Electric Field Cancer Treatment‐Enhanced Chemotherapy (LEFCT‐EC) with doxorubicin (10 mg/kg), and monitored for survival, and primary and metastatic tumors growth. RESULTS The electric field increased the uptake of doxorubicin by TRAMP cells in vitro. In vivo use of LEFCT‐EC reduced tumor size, prolonged survival, and cured 36–93% of the animals, dependent on treated tumor size. LEFCT‐EC was more effective than surgery with or without chemotherapy. Part of the cured animals developed anti‐tumor immunity and immunosuppression, significantly decreased the effectiveness of the treatment. CONCLUSION Our results suggest that LEFCT‐EC is an effective method for the destruction of metastatic prostate tumors. Prostate 66: 1620–1630, 2006. © 2006 Wiley‐Liss, Inc.
Bibliography:The Horowitz Research Fund
The Elsa and Leo Abramson Fund
ark:/67375/WNG-9T8ZXZ0S-K
The Israel Frida and Chaia Hamer Fund
istex:4B7C8F0259961A69DD1673B3D5E4F11E7EE65734
ArticleID:PROS20435
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0270-4137
1097-0045
DOI:10.1002/pros.20435