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2000
Volume 5, Issue 4
  • ISSN: 1574-888X
  • E-ISSN: 2212-3946

Abstract

In children, cancers are the deadliest of diseases and second only to accidents as the leading cause of death. The deadliest of the brain cancers are the malignant gliomas. Approximately two-thirds of children can survive less malignant types of brain cancers, however, in ~67% of these survivors recurs under the current regimes of surgery followed by administration of high doses toxic drugs and exposure to high doses of radiation. Even more distressing is that fortunate survivors are generally left with life-long cognitive disabilities. A new medical approach is desperately needed. Stem cells, with their natural ability to seek out brain tumors, could be used to accurately deliver therapy directly to the cancer sparing normal tissues for suppression of tumor growth. Despite exciting initial reports, clinical potency of stem cell therapy in animal brain tumor models has to date proven disappointing. Attempts to extrapolate the animal study results to humans are stymied by the fact that stem cells are heterogeneous, resulting in differences in their efficacy. Indeed, therapeutic success relies on an effective strategy to select for a stem cell sub-population within some particular stage of the development at which they are competitive and capable of targeting brain tumors. To improve this during developmental path, concept of a ‘therapeutic window’ is proposed. The “therapeutic window” for stem cells or more specifically a “biochemical therapeutic window” can be determined from biochemical assays and a “biological therapeutic window” from biological assays or even a molecular window from genetic description. Taken together, we can use selective processes to generate more effective stem cells to treat cancers as is clearly needed today.

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/content/journals/cscr/10.2174/157488810793351730
2010-12-01
2025-09-18
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  • Article Type:
    Research Article
Keyword(s): 3D collagen; adjuvant therapies; anti-tumor treatment; antiangiogenic antibody; antitumor efficacy; autologous stem cell transplantation; axon guidance; BBB permeabilization; biochemical mechanisms; biological behavior; biological therapeutic window; cancer cells; cancer satellite foci; CANCER-RELATED DEATH IN CHILDREN; cell development; central nervous system; chemokine receptors; chemokines; chemotherapeutic regimens; chemotherapy; clinical prognoses; clinical research; CNS cancers; cytotoxic therapies; Developmental Stage; drug dosage; embryonic organ transplantation; embryonic pig organ; embryonic stem cells; endoderm; enzymatic activities; genetic spectra; gestational stages; glioblastoma multiforme; healing pathways; heterogeneous; human blastocysts; HYPOTHESIS; Imaging techniques; immune regulatory functions; in vivo; inflammation; insulin-secreting capacity; intervention; intracranial brain tumor model; istological; laboratory assays; life cycle of cancer cells; long-term responses; lymphodepletion period; malignant astrocytoma; MALIGNANT BRAIN; matrix remodeling; maximal liver growth; mesoderm; metalloproteinases; microfluidic chambers; microsatellites; myocardial infarction; nerve injury; neural cell adhesion molecules; neuriteinducing factors; Neuro-oncology; neurological toxicity; neurons; neuroprotective properties; neurosurgeons; novel targeted therapies; oncologically; optimal gestational; organotypic brain; osmotic breaching of the blood-brain barrier (BBB); Pediatric brain tumor; pediatric hematological malignancies; pediatric medulloblastoma; pharmacokinetically; phenotypic analysis; pluripotent cells; postradiation; PRIMARY TREATMENT MODALITIES; prognostic tools; proliferation of polyclonal T cells; radiation therapy; respiratory system; secretion of matrix; spatial and temporal distribution of molecular lipo; stem cells; surgical resection; synthetic polymers; targeting brain tumors; teratoma formation; teratoma-free; therapeutic activation; therapeutic efficacy of stem cells; therapy; three dimensional (3D) system; tissue biopsy; transcriptome analyses; treatment of diabetes; tumor oxygenation; tumor-targeting; tumor-tracking; zymography
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