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Gene Therapy As a Potential Tool for Treating Neuroblastoma-a Focused Review

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Date 2016 Apr 16
PMID 27080224
Citations 6
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Abstract

Neuroblastoma, a solid tumor caused by rapid division of undifferentiated neuroblasts, is the most common childhood malignancy affecting children aged <5 years. Several approaches and strategies developed and tested to cure neuroblastoma have met with limited success due to different reasons. Many oncogenes are deregulated during the onset and development of neuroblastoma and thus offer an opportunity to circumvent this disease if the expression of these genes is restored to normalcy. Gene therapy is a powerful tool with the potential to inhibit the deleterious effects of oncogenes by inserting corrected/normal genes into the genome. Both viral and non-viral vector-based gene therapies have been developed and adopted to deliver the target genes into neuroblastoma cells. These attempts have given hope to bringing in a new regime of treatment against neuroblastoma. A few gene-therapy-based treatment strategies have been tested in limited clinical trials yielding some positive results. This mini review is an attempt to provide an overview of the available options of gene therapy to treat neuroblastoma.

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References
1.
Schlehofer J . The tumor suppressive properties of adeno-associated viruses. Mutat Res. 1994; 305(2):303-13. DOI: 10.1016/0027-5107(94)90250-x. View

2.
Farrell C, Zaupa C, Barnard Z, Maley J, Martuza R, Rabkin S . Combination immunotherapy for tumors via sequential intratumoral injections of oncolytic herpes simplex virus 1 and immature dendritic cells. Clin Cancer Res. 2008; 14(23):7711-6. PMC: 2670995. DOI: 10.1158/1078-0432.CCR-08-1364. View

3.
Kim N, Im K, Lim J, Jeon E, Nam Y, Kim E . Mesenchymal stem cells for the treatment and prevention of graft-versus-host disease: experiments and practice. Ann Hematol. 2013; 92(10):1295-308. DOI: 10.1007/s00277-013-1796-z. View

4.
Pesonen S, Helin H, Nokisalmi P, Escutenaire S, Ribacka C, Sarkioja M . Oncolytic adenovirus treatment of a patient with refractory neuroblastoma. Acta Oncol. 2009; 49(1):117-9. DOI: 10.3109/02841860903071369. View

5.
Parikh N, Currier M, Mahller Y, Adams L, Di Pasquale B, Collins M . Oncolytic herpes simplex virus mutants are more efficacious than wild-type adenovirus Type 5 for the treatment of high-risk neuroblastomas in preclinical models. Pediatr Blood Cancer. 2004; 44(5):469-78. DOI: 10.1002/pbc.20268. View