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  4. Sonoporation-mediated anti-angiogenic gene transfer into muscle effectively regresses distant orthotopic tumors
 
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Sonoporation-mediated anti-angiogenic gene transfer into muscle effectively regresses distant orthotopic tumors

Journal
Cancer Gene Therapy
Journal Volume
19
Journal Issue
3
Pages
171-180
Date Issued
2012
Author(s)
Liao Z.-K.
Tsai K.-C.
Wang H.-T.
SHENG-HONG TSENG  
Deng W.-P.
WEN-SHIANG CHEN  
Hwang L.-H.
DOI
10.1038/cgt.2011.73
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84857113870&doi=10.1038%2fcgt.2011.73&partnerID=40&md5=fd82f1db59bd2c5da23eee49baf4e645
https://scholars.lib.ntu.edu.tw/handle/123456789/481447
Abstract
Ultrasound (US) is an effective tool for local delivery of genes into target tumors or organs. In combination with microbubbles, US can temporarily change the permeability of cell membranes by cavitation and facilitate entry of plasmid DNA into cells. Here, we demonstrate that repeated US-mediated delivery of anti-angiogenic genes, endostatin or calreticulin, into muscle significantly inhibits the growth of orthotopic tumors in the liver, brain or lung. US-mediated anti-angiogenic gene therapy also seems to function as an adjuvant therapy that significantly enhances the antitumor effects of the chemotherapeutic drug doxorubicin and adenovirus-mediated cytokine gene therapy. Significantly higher levels of tumor apoptosis or tumor-infiltrating lymphocytes were observed after combined therapy consisting of either anti-angiogenic therapy and chemotherapy, or anti-angiogenic therapy and immunotherapy. Taken together, our experiments demonstrate that intramuscular delivery of anti-angiogenic genes by US exposure can effectively treat distant orthotopic tumors, and thus has great therapeutic potential in terms of clinical treatment. ? 2012 Nature America, Inc. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
adenovirus vector; calreticulin; doxorubicin; endostatin; granulocyte macrophage colony stimulating factor; interleukin 12; sonovue; animal cell; animal experiment; animal model; animal tissue; antiangiogenic gene therapy; antineoplastic activity; apoptosis; article; brain tumor; cancer adjuvant therapy; cancer combination chemotherapy; cancer gene therapy; cancer immunotherapy; controlled study; drug intermittent therapy; drug potentiation; gene expression; human; human cell; liver tumor; lung tumor; male; monotherapy; mouse; nonhuman; nonviral gene delivery system; priority journal; rat; sonoporation mediated antiangiogenic gene therapy; transgene; tumor associated leukocyte; tumor regression; ultrasound; Adenoviridae
Type
journal article

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