| Literature DB >> 35288093 |
Margot Revel1, Catherine Sautès-Fridman1, Wolf-Herman Fridman1, Lubka T Roumenina2.
Abstract
The omics era made possible the quest for efficient markers for cancer progression and revealed that macrophage populations are much more complex than just the M1/M2 dichotomy. Complement C1q pops up as a marker of a tolerogenic and immunosuppressive macrophage populations in both healthy and tumor tissues, but the specific role of C1q+ tumor-associated macrophages (TAM) is poorly understood. C1q is co-expressed in healthy and tumor macrophages with human leukocyte antigen DR (HLA-DR), Apolipoprotein E (APOE), and mannose receptor C-type 1 (MRC1) (CD206), suggesting a resident origin of this population. TAM expressing C1q correlate with T cell exhaustion and poor prognosis in numerous cancers. Herein, we discuss the plural roles of C1q in these macrophages and how it could drive cancer progression.Entities:
Keywords: C1q; T cell exhaustion; complement system; tumor-associated macrophages
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Year: 2022 PMID: 35288093 DOI: 10.1016/j.trecan.2022.02.006
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025