Back to Search
Start Over
ELECTROPORATION INCREASES ANTITUMORAL EFFICACY OF THE BCl-2 ANTISENSE G3139 AND CHEMOTHERAPY IN A HUMAN MELANOMA XENOGRAFT
- Source :
- ResearcherID, Journal of Translational Medicine, Vol 9, Iss 1, p 125 (2011), Journal of Translational Medicine
-
Abstract
- Background Nucleic acids designed to modulate the expression of target proteins remain a promising therapeutic strategy in several diseases, including cancer. However, clinical success is limited by the lack of efficient intracellular delivery. In this study we evaluated whether electroporation could increase the delivery of antisense oligodeoxynucleotides against bcl-2 (G3139) as well as the efficacy of combination chemotherapy in human melanoma xenografts. Methods Melanoma-bearing nude mice were treated i.v. with G3139 and/or cisplatin (DDP) followed by the application of trains of electric pulses to tumors. Western blot, immunohistochemistry and real-time PCR were performed to analyze protein and mRNA expression. The effect of electroporation on muscles was determined by histology, while tumor apoptosis and the proliferation index were analyzed by immunohistochemistry. Antisense oligodeoxynucleotides tumor accumulation was measured by FACS and confocal microscopy. Results The G3139/Electroporation combined therapy produced a significant inhibition of tumor growth (TWI, more than 50%) accompanied by a marked tumor re-growth delay (TRD, about 20 days). The efficacy of this treatment was due to the higher G3139 uptake in tumor cells which led to a marked down-regulation of bcl-2 protein expression. Moreover, the G3139/EP combination treatment resulted in an enhanced apoptotic index and a decreased proliferation rate of tumors. Finally, an increased tumor response was observed after treatment with the triple combination G3139/DDP/EP, showing a TWI of about 75% and TRD of 30 days. Conclusions These results demonstrate that electroporation is an effective strategy to improve the delivery of antisense oligodeoxynucleotides within tumor cells in vivo and it may be instrumental in optimizing the response of melanoma to chemotherapy. The high response rate observed in this study suggest to apply this strategy for the treatment of melanoma patients.
- Subjects :
- Proliferation index
Down-Regulation
lcsh:Medicine
Antineoplastic Agents
Apoptosis
Pharmacology
Biology
General Biochemistry, Genetics and Molecular Biology
Mice
In vivo
Cell Line, Tumor
medicine
Animals
Humans
RNA, Messenger
Muscle, Skeletal
Electrodes
Melanoma
Cell Proliferation
Cisplatin
Medicine(all)
Biochemistry, Genetics and Molecular Biology(all)
Electroporation
Research
lcsh:R
Cancer
Combination chemotherapy
General Medicine
Oligonucleotides, Antisense
Thionucleotides
medicine.disease
Combined Modality Therapy
Xenograft Model Antitumor Assays
Neoplasm Proteins
Gene Expression Regulation, Neoplastic
Treatment Outcome
Proto-Oncogene Proteins c-bcl-2
medicine.drug
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- ResearcherID, Journal of Translational Medicine, Vol 9, Iss 1, p 125 (2011), Journal of Translational Medicine
- Accession number :
- edsair.doi.dedup.....c8a075e6ecccecb0ce6d7d348704cc92