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Targeting the Complement Pathway in Malignant Glioma Microenvironments

Hongtao Zhu, Xingjiang Yu, Suojun Zhang +1 more2021Frontiers in Cell and Developmental BiologyReview
10.3389/fcell.2021.657472PubMedFree full text
Immune/InnateNeurological

Abstract

Malignant glioma is a highly fatal type of brain tumor, and its reoccurrence is largely due to the ordered interactions among the components present in the complex microenvironment. Besides its role in immune surveillance and clearance under physiological conditions, the complement system is expressed in a variety of tumor types and mediates the interactions within the tumor microenvironments. Recent studies have uncovered the broad expression spectrum of complement signaling molecules in the tumor microenvironment and various tumor cells, in particular, malignant glioma cells. Involvement of the complement system in tumor growth, immunosuppression and phenotype transition have also been elucidated. In this review, we enumerate the expression and function of complement molecules in multiple tumor types reported. Moreover, we elaborate the complement pathways in glioma cells and various components of malignant glioma microenvironments. Finally, we summarize the possibility of the complement molecules as prognostic factors and therapeutic targets in the treatment of malignant glioma. Specific targeting of the complement system maybe of great significance and value in the future treatment of multi-type tumors including malignant glioma.

References (2)

  • Identification and characterization of the complement C5a anaphylatoxin receptor on human astrocytesThe Journal of Immunology · 1995
  • Differential regulation of C3 gene expression in human astroglioma cells by interferon-γ and interleukin-1βNeuroscience Letters · 1995

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