Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014:2014:549136.
doi: 10.1155/2014/549136. Epub 2014 Jul 10.

Stem cell based gene therapy in prostate cancer

Affiliations
Review

Stem cell based gene therapy in prostate cancer

Jae Heon Kim et al. Biomed Res Int. 2014.

Abstract

Current prostate cancer treatment, especially hormone refractory cancer, may create profound iatrogenic outcomes because of the adverse effects of cytotoxic agents. Suicide gene therapy has been investigated for the substitute modality for current chemotherapy because it enables the treatment targeting the cancer cells. However the classic suicide gene therapy has several profound side effects, including immune-compromised due to viral vector. Recently, stem cells have been regarded as a new upgraded cellular vehicle or vector because of its homing effects. Suicide gene therapy using genetically engineered mesenchymal stem cells or neural stem cells has the advantage of being safe, because prodrug administration not only eliminates tumor cells but consequently kills the more resistant therapeutic stem cells as well. The attractiveness of prodrug cancer gene therapy by stem cells targeted to tumors lies in activating the prodrug directly within the tumor mass, thus avoiding systemic toxicity. Therapeutic achievements using stem cells in prostate cancer include the cytosine deaminase/5-fluorocytosine prodrug system, herpes simplex virus thymidine kinase/ganciclovir, carboxyl esterase/CPT11, and interferon-beta. The aim of this study is to review the stem cell therapy in prostate cancer including its proven mechanisms and also limitations.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Pulkkanen KJ, Yla-Herttuala S. Gene therapy for malignant glioma: current clinical status. Molecular Therapy. 2005;12(4):585–598. - PubMed
    1. Cihova M, Altanerova V, Altaner C. Stem cell based cancer gene therapy. Molecular Pharmaceutics. 2011;8(5):1480–1487. - PubMed
    1. Zarogoulidis P, Darwiche K, Sakkas A, et al. Suicide gene therapy for cancer—current strategies. Journal of Genetic Syndrome & Gene Therapy. 2013;9:p. 4. - PMC - PubMed
    1. Bobis S, Jarocha D, Majka M. Mesenchymal stem cells: characteristics and clinical applications. Folia Histochemica et Cytobiologica. 2006;44(4):215–230. - PubMed
    1. Borlongan CV, Kaneko Y, Maki M, et al. Menstrual blood cells display stem cell-like phenotypic markers and exert neuroprotection following transplantation in experimental stroke. Stem Cells and Development. 2010;19(4):439–452. - PMC - PubMed

Publication types