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C1q+ 巨噬细胞:癌症进展的乘客还是驱动者?

C1q+ macrophages: passengers or drivers of cancer progression.

机构信息

Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, F-75006 Paris, France.

Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, F-75006 Paris, France.

出版信息

Trends Cancer. 2022 Jul;8(7):517-526. doi: 10.1016/j.trecan.2022.02.006. Epub 2022 Mar 12.

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.

摘要

组学时代使得寻找癌症进展的有效标志物成为可能,并揭示了巨噬细胞群体远比 M1/M2 二分法复杂。补体 C1q 作为健康组织和肿瘤组织中耐受性和免疫抑制性巨噬细胞群体的标志物出现,但 C1q+肿瘤相关巨噬细胞(TAM)的具体作用尚不清楚。C1q 与人类白细胞抗原 DR(HLA-DR)、载脂蛋白 E(APOE)和甘露糖受体 C 型 1(MRC1)(CD206)在健康和肿瘤巨噬细胞中共表达,表明该群体具有驻留起源。在许多癌症中,表达 C1q 的 TAM 与 T 细胞耗竭和预后不良相关。本文讨论了 C1q 在这些巨噬细胞中的多重作用以及它如何促进癌症进展。

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