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Context-Dependent Glioblastoma?Macrophage/Microglia Symbiosis and Associated Mechanisms

Journal

TRENDS IN IMMUNOLOGY
Volume 42, Issue 4, Pages 280-292

Publisher

CELL PRESS
DOI: 10.1016/j.it.2021.02.004

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Funding

  1. NIH [R00 CA240896, P50 CA221747]
  2. Northwestern University

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This article discusses how intrinsic alterations in tumor cells affect the biology of immune cells and how these immune cells support tumor progression. Studying the relationship between GBM and GAM can reveal the molecular basis of GBM tumorigenesis and lead to new treatment approaches to improve patient outcomes.
Glioblastoma (GBM) is a lethal form of primary brain tumor in human adults. The impact of tumor-intrinsic alterations is not exclusively confined to cancer cells but can also be extended to the tumor microenvironment (TME). Glioblastomaassociated macrophages/microglia (GAMs) are a prominent type of immune cells that account for up to 50% of total cells in GBM. Emerging evidence suggests that context-dependent GBM?GAM symbiotic interactions are pivotal for tumor growth and progression. Here, we discuss how specific genetic alterations in GBM cells affect GAM biology and, reciprocally, how GAMs support GBM progression. We hypothesize that understanding context-dependent GBM?GAM symbiosis may reveal the molecular basis of GBM tumorigenesis and lead to novel candidate treatment approaches aiming to improve GBM patient outcomes.

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