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The role of microglia and macrophages in glioma maintenance and progression

Journal

NATURE NEUROSCIENCE
Volume 19, Issue 1, Pages 20-27

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nn.4185

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Funding

  1. Deutsche Forschungsgemeinschaft [TR 43, KE 329/30-1]
  2. Neurocure
  3. Department of Defense [W81XWH-13-1-0094]
  4. James S. McDonnell Foundation
  5. National Cancer Institute [U01-CA160882]
  6. NATIONAL CANCER INSTITUTE [U01CA160882] Funding Source: NIH RePORTER

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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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