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Marked regression of liver metastasis by combined therapy of ultrasound-mediated NF kappaB-decoy transfer and transportal injection of paclitaxel, in mouse.
- Source :
-
International journal of cancer [Int J Cancer] 2008 Apr 01; Vol. 122 (7), pp. 1645-56. - Publication Year :
- 2008
-
Abstract
- Nuclear factor-kappaB (NF kappaB) plays a pivotal role in cancer progression. In this study, we developed a decoy cis-element oligo-deoxyribonucleic acid against NF kappaB-binding site (NF kappaB-decoy), which effectively inhibits NF kappaB activity, and tested the effect of combined therapy comprising local transfection of NF kappaB-decoy into the liver and transportal injection of paclitaxel on cancer growth and metastasis using an orthotopic murine model of colon cancer liver metastasis. For NF kappaB-decoy transfection, we employed a novel approach using ultrasound exposure with an echocardiographic contrast agent, Optison. We examined the influence of NF kappaB-decoy transfer on susceptibility to paclitaxel in cancer cells and the mechanism involved using several in vitro analysis systems. We then studied the in vivo effect of combined NF kappaB-decoy transfer and paclitaxel in preventing cancer progression using a murine model of liver metastasis created by splenic injection of a human colon cancer cell line, HT29. In vitro experiments, including MTT-assay, fluorescence-activated cell sorter and cDNA array analysis, revealed that NF kappaB-decoy transfer significantly increased the susceptibility of cancer cells to paclitaxel, and that decreased expression of anti-apoptotic genes along with increased expression of genes relevant to the apoptosis-promotor may be involved. In vivo experiments showed that local transfection of NF kappaB-decoy into the liver followed by portal injection of paclitaxel effectively induced cancer cell apoptosis in the liver metastasis, and significantly prolonged animal survival compared to controls, without notable side effects. In conclusion, a combination of local NF kappaB-decoy transfer into the liver and transportal injection of paclitaxel may be a safe and effective new therapy for liver metastasis.<br /> ((c) 2007 Wiley-Liss, Inc.)
- Subjects :
- Animals
Antineoplastic Agents, Phytogenic pharmacology
Apoptosis
Cell Line, Tumor
Chemotherapy, Adjuvant
Colorimetry
Down-Regulation
Flow Cytometry
Gene Expression Regulation, Neoplastic
Humans
Immunoblotting
Injections, Intravenous
Liver Neoplasms diagnostic imaging
Liver Neoplasms drug therapy
Mice
Mice, Inbred BALB C
Mice, Nude
Microscopy, Fluorescence
NF-kappa B metabolism
Oligodeoxyribonucleotides administration & dosage
Oligonucleotide Array Sequence Analysis
Paclitaxel pharmacology
Portal Vein
Random Allocation
Reverse Transcriptase Polymerase Chain Reaction
Ultrasonography
Antineoplastic Agents, Phytogenic administration & dosage
Colonic Neoplasms pathology
Genetic Therapy methods
Liver Neoplasms secondary
Liver Neoplasms therapy
NF-kappa B antagonists & inhibitors
Paclitaxel administration & dosage
Transfection methods
Ultrasonics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-0215
- Volume :
- 122
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- International journal of cancer
- Publication Type :
- Academic Journal
- Accession number :
- 18058816
- Full Text :
- https://doi.org/10.1002/ijc.23280