Abstract |
Strategies targeting the microenvironment of pediatric brain cancers have the potential to improve the efficacy of standard and genome-based molecular therapeutics. These strategies also have the potential of helping resolve many of the challenges associated with developing new drugs and running clinical trials for relatively small pediatric brain tumor population. Disrupting vital paracrine and physical interactions between cancer cells and surrounding stroma, targeting and normalizing the abnormal tumor vasculature, and/or inducing antitumor immunity represent some of the most promising approaches. A comprehensive characterization of the pediatric brain tumor microenvironment's composition and function and its modulation by chemoradiation and molecularly targeted therapies is warranted to develop and effectively implement these approaches.
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Authors | Ana Batista, Lars Riedemann, Trupti Vardam, Rakesh K Jain |
Journal | Cancer journal (Sudbury, Mass.)
(Cancer J)
2015 Jul-Aug
Vol. 21
Issue 4
Pg. 307-13
ISSN: 1540-336X [Electronic] United States |
PMID | 26222083
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Angiogenesis Inhibitors
- Antineoplastic Agents
- Cell Adhesion Molecules, Neuronal
- Membrane Proteins
- Nerve Tissue Proteins
- PIGF protein, human
- neuroligin 3
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Topics |
- Angiogenesis Inhibitors
(therapeutic use)
- Antineoplastic Agents
- Brain Neoplasms
(blood supply, drug therapy, immunology)
- Cell Adhesion Molecules, Neuronal
(metabolism)
- Child
- Glioma
(blood supply, drug therapy, immunology)
- Humans
- Immunomodulation
- Medulloblastoma
(blood supply, drug therapy, immunology)
- Membrane Proteins
(metabolism)
- Molecular Targeted Therapy
- Neovascularization, Pathologic
(drug therapy)
- Nerve Tissue Proteins
(metabolism)
- Paracrine Communication
- Tumor Microenvironment
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