» Articles » PMID: 19430884

Gene Therapy As an Adjuvant Treatment for Malignant Gliomas: from Bench to Bedside

Overview
Journal J Neurooncol
Publisher Springer
Date 2009 May 12
PMID 19430884
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Malignant brain tumors, including high-grade gliomas, are among the most lethal of all cancers. Despite considerable advances, including multi-modality treatments with surgery, radiotherapy, and chemotherapy, the overall prognosis for patients with this disease remains dismal. Currently available treatments necessitate the development of more effective tumor-selective therapies. The use of gene therapy for brain tumor therapy is promising as it can be delivered in situ and selectively targets brain tumor cells while sparing the adjacent normal brain tissue. In this article, we summarize the laboratory and clinical work using viral, cell-based, and synthetic vectors, as well as other strategies focused on potentiate gene delivery. Although tangible results on patients' survival remains to be further documented, significant advances in therapeutic gene transfer strategies have been made. The enthusiasm of this progress needs to be tempered by the realistic assessment of the challenges needed to be overcome. Finally, as the field of gene delivery progresses, advances must be made in identifying genes and proteins key to the treatment of malignant gliomas. Due to the great heterogeneity of malignant glioma cells, only approaches combining different strategies may be ultimately successful in defeating this disease.

Citing Articles

Expression of eIF4E Gene in Glioma and Its Sensitivity to Oxidative Stress.

Liang J, Yang Y, Li X, Cai G, Cao J, Zhang B Oxid Med Cell Longev. 2022; 2022:5413035.

PMID: 36225177 PMC: 9550436. DOI: 10.1155/2022/5413035.


Human iPSC for Therapeutic Approaches to the Nervous System: Present and Future Applications.

Cefalo M, Carai A, Miele E, Po A, Ferretti E, Mastronuzzi A Stem Cells Int. 2015; 2016:4869071.

PMID: 26697076 PMC: 4677260. DOI: 10.1155/2016/4869071.


Stem cells and gliomas: past, present, and future.

Germano I, Binello E J Neurooncol. 2014; 119(3):547-55.

PMID: 25081973 DOI: 10.1007/s11060-014-1498-y.


"Footprint-free" human induced pluripotent stem cell-derived astrocytes for in vivo cell-based therapy.

Mormone E, DSousa S, Alexeeva V, Bederson M, Germano I Stem Cells Dev. 2014; 23(21):2626-36.

PMID: 24914471 PMC: 4201311. DOI: 10.1089/scd.2014.0151.


A peptide-mediated targeting gene delivery system for malignant glioma cells.

Wang C, Ning L, Wang H, Lu Z, Li X, Fan X Int J Nanomedicine. 2013; 8:3631-40.

PMID: 24101872 PMC: 3790891. DOI: 10.2147/IJN.S44990.


References
1.
Lawler S, Peruzzi P, Chiocca E . Genetic strategies for brain tumor therapy. Cancer Gene Ther. 2005; 13(3):225-33. DOI: 10.1038/sj.cgt.7700886. View

2.
Zarnitsyn V, Kamaev P, Prausnitz M . Ultrasound-enhanced chemotherapy and gene delivery for glioma cells. Technol Cancer Res Treat. 2007; 6(5):433-42. DOI: 10.1177/153303460700600509. View

3.
Maleniak T, Darling J, Lowenstein P, Castro M . Adenovirus-mediated expression of HSV1-TK or Fas ligand induces cell death in primary human glioma-derived cell cultures that are resistant to the chemotherapeutic agent CCNU. Cancer Gene Ther. 2001; 8(8):589-98. DOI: 10.1038/sj.cgt.7700348. View

4.
Lee J, Elkahloun A, Messina S, Ferrari N, Xi D, Smith C . Cellular and genetic characterization of human adult bone marrow-derived neural stem-like cells: a potential antiglioma cellular vector. Cancer Res. 2003; 63(24):8877-89. View

5.
Yoshida J, Mizuno M, Fujii M, Kajita Y, Nakahara N, Hatano M . Human gene therapy for malignant gliomas (glioblastoma multiforme and anaplastic astrocytoma) by in vivo transduction with human interferon beta gene using cationic liposomes. Hum Gene Ther. 2004; 15(1):77-86. DOI: 10.1089/10430340460732472. View