Targeted therapy of brain tumors utilizing neural stem and progenitor cells

被引:9
作者
Burns, MJ [1 ]
Weiss, W [1 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2003年 / 8卷
关键词
C17.2; neural stem cells; brain tumor; targeted therapy; neural progenitors; review;
D O I
10.2741/953
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neural stem and progenitor cells derived from the central nervous system (CNS) of embryonic and adult mammals share three critical features: 1. Stem and progenitor cells are highly migratory, 2. Stem and progenitor cells have affinity for areas of CNS pathology, and 3. The pluripotentcy of neural stem and progenitor cells allows them to engraft and replace damaged tissues in the CNS. These properties suggest that transplanted neural stem cells might be used to deliver molecular therapy to diseased regions of the nervous system, and to regenerate lost tissues. One of the greatest challenges and potential promises of stem cell therapy is to direct therapy to pathological tissues comprised of cells which themselves are migratory. The ability of glioma cells to migrate extensively into normal brain parenchyma in part underlies the lethal nature of these tumors. A better understanding of the mechanisms by which neural stem cells migrate to specific sources of injury may allow us to harness these cells as vehicles for delivery of molecular therapies to impact survival in patients with recalcitrant gliomas.
引用
收藏
页码:E228 / E234
页数:7
相关论文
共 61 条
[11]   AXONAL ELONGATION INTO PERIPHERAL NERVOUS-SYSTEM BRIDGES AFTER CENTRAL NERVOUS-SYSTEM INJURY IN ADULT-RATS [J].
DAVID, S ;
AGUAYO, AJ .
SCIENCE, 1981, 214 (4523) :931-933
[12]   HUMAN AMNION MEMBRANE SERVES AS A SUBSTRATUM FOR GROWING AXONS INVITRO AND INVIVO [J].
DAVIS, GE ;
BLAKER, SN ;
ENGVALL, E ;
VARON, S ;
MANTHORPE, M ;
GAGE, FH .
SCIENCE, 1987, 236 (4805) :1106-1109
[13]   Blastula-stage stem cells can differentiate into dopaminergic and serotonergic neurons after transplantation [J].
Deacon, T ;
Dinsmore, J ;
Costantini, LC ;
Ratliff, J ;
Isacson, O .
EXPERIMENTAL NEUROLOGY, 1998, 149 (01) :28-41
[14]   Glioma migration: clues from the biology of neural progenitor cells and embryonic CNS cell migration [J].
Dirks, PB .
JOURNAL OF NEURO-ONCOLOGY, 2001, 53 (02) :203-212
[15]   Subventricular zone astrocytes are neural stem cells in the adult mammalian brain [J].
Doetsch, F ;
Caillé, I ;
Lim, DA ;
García-Verdugo, JM ;
Alvarez-Buylla, A .
CELL, 1999, 97 (06) :703-716
[16]   Engraftable human neural stem cells respond to developmental cues, replace neurons, and express foreign genes [J].
Flax, JD ;
Aurora, S ;
Yang, CH ;
Simonin, C ;
Wills, AM ;
Billinghurst, LL ;
Jendoubi, M ;
Sidman, RL ;
Wolfe, JH ;
Kim, SU ;
Snyder, EY .
NATURE BIOTECHNOLOGY, 1998, 16 (11) :1033-1039
[17]   TRANSPLANTATION OF B16/C3 MELANOMA-CELLS INTO THE BRAINS OF RATS AND MICE [J].
FREED, WJ ;
ADINOLFI, AM ;
LASKIN, JD ;
GELLER, HM .
BRAIN RESEARCH, 1989, 485 (02) :349-362
[18]   Mammalian neural stem cells [J].
Gage, FH .
SCIENCE, 2000, 287 (5457) :1433-1438
[19]   UNITED-PARKINSON-FOUNDATION NEUROTRANSPLANTATION REGISTRY ON ADRENAL-MEDULLARY TRANSPLANTS - PRESURGICAL, AND 1-YEAR AND 2-YEAR FOLLOW-UP [J].
GOETZ, CG ;
STEBBINS, GT ;
KLAWANS, HL ;
KOLLER, WC ;
GROSSMAN, RG ;
BAKAY, RAE ;
PENN, RD .
NEUROLOGY, 1991, 41 (11) :1719-1722
[20]   Adult-generated hippocampal and neocortical neurons in macaques have a transient existence [J].
Gould, E ;
Vail, N ;
Wagers, M ;
Gross, CG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10910-10917