Targeting of melanoma brain metastases using engineered neural stem/progenitor cells

被引:119
作者
Aboody, KS
Najbauer, J
Schmidt, NO
Yang, W
Wu, JK
Zhuge, Y
Przylecki, W
Carroll, R
Black, PM
Perides, G
机构
[1] City Hope Natl Med Ctr, Div Hematol & Hematopoiet Cell Transplantat, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Div Neurosci, Duarte, CA 91010 USA
[3] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Neurosurg,Neurosurg Oncol Lab, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Childrens Hosp, Boston, MA 02115 USA
[6] Univ Hamburg, Hosp Eppendorf, Dept Neurosurg, D-20246 Hamburg, Germany
[7] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA 02215 USA
[8] Tufts Univ, Sch Med, Boston, MA 02111 USA
[9] Tufts Univ, New England Med Ctr, Dept Surg, Boston, MA 02111 USA
[10] Tufts Univ, New England Med Ctr, Dept Neurosurg, Boston, MA 02111 USA
关键词
brain metastases; cytosine deaminase; gene therapy; melanoma; neural progenitor cells; neural stem cells; tumor targeting;
D O I
10.1215/15228517-2005-012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Brain metastases are an increasingly frequent and serious clinical problem for cancer patients, especially those with advanced melanoma. Given the extensive tropism of neural stem/progenitor cells (NSPCs) for pathological areas in the central nervous system, we expanded investigations to determine whether NSPCs could also target multiple sites of brain metastases In a syngeneic experimental melanoma model. Using cytosine deaminase-expressing NSPCs (CD-NSPCs) and systemic 5-fluorocytosine (5-FC) pro-drug administration, we explored their potential as a cell-based targeted drug delivery system to disseminated brain metastases. Our results indicate a strong tropism of NSPCs for intracerebral melanoma metastases. Furthermore, in our therapeutic paradigm, animals with established melanoma brain metastasis received intracranial implantation of CD-NSPCs followed by systemic 5-FC treatment, resulting in a significant (71%) reduction in tumor burden. These data provide proof of principle for the use of NSPCs for targeted delivery of therapeutic gene products to melanoma brain metastases.
引用
收藏
页码:119 / 126
页数:8
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