Abstract |
There is a growing recognition that gliomas are complex tumors composed of neoplastic and non-neoplastic cells, which each individually contribute to cancer formation, progression and response to treatment. The majority of the non-neoplastic cells are tumor-associated macrophages (TAMs), either of peripheral origin or representing brain-intrinsic microglia, that create a supportive stroma for neoplastic cell expansion and invasion. TAMs are recruited to the glioma environment, have immune functions, and can release a wide array of growth factors and cytokines in response to those factors produced by cancer cells. In this manner, TAMs facilitate tumor proliferation, survival and migration. Through such iterative interactions, a unique tumor ecosystem is established, which offers new opportunities for therapeutic targeting.
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Authors | Dolores Hambardzumyan, David H Gutmann, Helmut Kettenmann |
Journal | Nature neuroscience
(Nat Neurosci)
Vol. 19
Issue 1
Pg. 20-7
(Jan 2016)
ISSN: 1546-1726 [Electronic] United States |
PMID | 26713745
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Review)
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Topics |
- Animals
- Central Nervous System Neoplasms
(immunology, metabolism, pathology)
- Disease Progression
- Glioma
(immunology, metabolism, pathology)
- Humans
- Macrophages
(immunology, metabolism, pathology)
- Microglia
(immunology, metabolism, pathology)
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