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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Systemic TNFα gene therapy synergizes with liposomal doxorubicine in the treatment of metastatic cancer.
Mol. Ther. 21, 300-308 (2013)
Tumor necrosisfactor alpha (TNF alpha) is a potent antitumoral cytokine, either killing tumor cells directly or affecting the tumor vasculature leading to enhanced accumulation of macromolecular drugs. Due to dose limiting side effects systemic administration of TNF alpha protein at therapeutically active doses is precluded. With gene vectors, tumor restricted TNF alpha expression can be achieved and in principle synergize with chemotherapy. Synthetic gene carriers based on polyamines were intravenously injected, which either passively accumulate within the tumor or specifically target the epidermal growth factor receptor. A single intravenous injection of TNF alpha gene vector promoted accumulation of liposomal doxorubicine (Doxil) in murine neuroblastoma and human hepatoma by enhancing tumor endothelium permeability. The expression of transgenic TNF alpha was restricted to tumor tissue. Three treatment cycles with TNF alpha gene vectors and Doxil significantly delayed tumor growth in subcutaneous murine Neuro2A neuroblastoma. Also tumors re-growing after initial treatment were successfully treated in a fourth cycle pointing at the absence of resistance mechanisms. Systemic Neuro2A metastases or human LS174T colon carcinoma metastases in liver were also successfully treated with this combined approach. In conclusion, this schedule opens the possibility for the efficient treatment of tumors metastases otherwise not accessible for macromolecular drug carriers.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Tumor-necrosis-factor ; Growth-factor Receptor ; Iodide Symporter Gene ; Antitumor-activity ; Liver-cancer ; Plasmid Dna ; Kappa-b ; Delivery ; Vectors ; Cells
ISSN (print) / ISBN
1525-0016
e-ISSN
1525-0024
Zeitschrift
Molecular Therapy
Quellenangaben
Band: 21,
Heft: 2,
Seiten: 300-308
Verlag
Nature Publishing Group
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Molecular Immunology (IMI)