Stem cell based glioblastoma gene therapy

被引:26
作者
Altaner, C. [1 ]
Altanerova, V. [1 ]
机构
[1] Canc Res Inst SAS, Bratislava, Slovakia
关键词
glioblastoma; glioblastoma stem cells; chemoresistance; radio-resistance; stem cell driven gene therapy; prodrug gene therapy; preclinical studies; MARROW STROMAL CELLS; MALIGNANT GLIOMA; DELIVERY; GROWTH; TUMORS;
D O I
10.4149/neo_2012_95
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
There is no curative therapy for glioblastoma multiforme (GBM) thus far. Combined therapies including surgery, followed by concomitant irradiation and chemotherapy with the DNA alkylating agent temozolomide (TMZ), slightly improves patients' survival but the prognosis remains poor. The fatal nature of glioblastoma is caused by tumor-initiating glioblastoma cells. The tumor tropic ability of adult mesenchymal stem cells offers the attractive possibility to use these cells as a vehicle to deliver therapeutic agents to the site of the tumor. In preclinical studies using animal models, mesenchymal stem cells engineered to express suicide genes were shown to elicit a significant antitumor response against various tumors including glioblastoma. This review summarizes the current state of knowledge about stem cell directed glioblastoma therapy. Results obtained in a preclinical study using mesenchymal stem cells engineered to express cytosine deaminase provided evidence that stem cell based gene therapy might also attack glioblastoma stem cells and therefore be curative. In addition to stem cell directed prodrug gene therapies, other immunotherapeutic modalities using mesenchymal stem cells are discussed as well. Encouraging results of preclinical studies of stem cell based gene therapy for glioblastoma support the argument to begin clinical studies.
引用
收藏
页码:756 / 760
页数:5
相关论文
共 37 条
[1]
Stem and progenitor cell-mediated tumor selective gene therapy [J].
Aboody, K. S. ;
Najbauer, J. ;
Danks, M. K. .
GENE THERAPY, 2008, 15 (10) :739-752
[2]
Alkylpurine-DNA-N-glycosylase confers resistance to temozolomide in xenograft models of glioblastoma multiforme and is associated with poor survival in patients [J].
Agnihotri, Sameer ;
Gajadhar, Aaron S. ;
Ternamian, Christian ;
Gorlia, Thierry ;
Diefes, Kristin L. ;
Mischel, Paul S. ;
Kelly, Joanna ;
McGown, Gail ;
Thorncroft, Mary ;
Carlson, Brett L. ;
Sarkaria, Jann N. ;
Margison, Geoffrey P. ;
Aldape, Kenneth ;
Hawkins, Cynthia ;
Hegi, Monika ;
Guha, Abhijit .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (01) :253-266
[3]
Altaner C, 2008, NEOPLASMA, V55, P369
[4]
Human adipose tissue-derived mesenchymal stem cells expressing yeast cytosinedeaminase::uracil phosphoribosyltransferase inhibit intracerebral rat glioblastoma [J].
Altanerova, Veronika ;
Cihova, Marina ;
Babic, Michal ;
Rychly, Boris ;
Ondicova, Katarina ;
Mravec, Boris ;
Altaner, Cestmir .
INTERNATIONAL JOURNAL OF CANCER, 2012, 130 (10) :2455-2463
[5]
Use of genetically engineered bone marrow-derived mesenchymal stem cells for glioma gene therapy [J].
Amano, Shinji ;
Li, Shaoyi ;
Gu, Chunyu ;
Gao, Yun ;
Koizumi, Shinichiro ;
Yamamoto, Seiji ;
Terakawa, Susumu ;
Namba, Hiroki .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 35 (06) :1265-1270
[6]
Baculovirus-transduced bone marrow mesenchymal stem cells for systemic cancer therapy [J].
Bak, X. Y. ;
Yang, J. ;
Wang, S. .
CANCER GENE THERAPY, 2010, 17 (10) :721-729
[7]
Toward Brain Tumor Gene Therapy Using Multipotent Mesenchymal Stromal Cell Vectors [J].
Bexell, Daniel ;
Scheding, Stefan ;
Bengzon, Johan .
MOLECULAR THERAPY, 2010, 18 (06) :1067-1075
[8]
Bone Marrow Multipotent Mesenchymal Stroma Cells Act as Pericyte-like Migratory Vehicles in Experimental Gliomas [J].
Bexell, Daniel ;
Gunnarsson, Salina ;
Tormin, Ariane ;
Darabi, Anna ;
Gisselsson, David ;
Roybon, Laurent ;
Scheding, Stefan ;
Bengzon, Johan .
MOLECULAR THERAPY, 2009, 17 (01) :183-190
[9]
Adipose Tissue-derived Mesenchymal Stem Cells Expressing Prodrug-converting Enzyme Inhibit Human Prostate Tumor Growth [J].
Cavarretta, Ilaria T. ;
Altanerova, Veronika ;
Matuskova, Miroslava ;
Kucerova, Lucia ;
Culig, Zoran ;
Altaner, Cestmir .
MOLECULAR THERAPY, 2010, 18 (01) :223-231
[10]
NEURAL STEM/PROGENITORS AND GLIOMA STEM-LIKE CELLS HAVE DIFFERENTIAL SENSITIVITY TO CHEMOTHERAPY Reply [J].
Bota, Daniela A. ;
Linskey, Mark E. ;
Schwartz, Philip H. .
NEUROLOGY, 2011, 77 (22) :E135-E136