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TREM2 在癌症中的治疗潜力

英文原题:The therapeutic potential of TREM2 in cancer.

查看英文原题

The therapeutic potential of TREM2 in cancer.

PubMed 2022/09/02(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

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中文摘要

癌症仍是美国及全球重要的健康问题和主要死因,因此持续探索新型治疗靶点和联合疗法十分重要。髓系细胞触发受体2(TREM2)是免疫球蛋白超家族的跨膜受体,可与DNAX活化蛋白12(DAP12)和DAP10结合,将信号传递至细胞内。TREM2主要被认为表达于单核细胞-巨噬细胞谱系细胞;既往研究大多聚焦于其在阿尔茨海默病中的小胶质细胞功能。然而,随着TREM2研究拓展至癌症领域,研究人员发现,上皮性肿瘤细胞、瘤内巨噬细胞和髓系调节细胞也可表达TREM2。本文讨论上皮性肿瘤细胞表达TREM2时,可能产生抑癌或促癌作用的证据;同时介绍表达TREM2的瘤内巨噬细胞所发挥的免疫抑制作用,以及联合免疫检查点治疗靶向TREM2的治疗潜力。总体而言,现有文献提示,TREM2可作为某些癌症的新型潜在治疗靶点。

展开英文摘要原文

Cancer continues to be a substantial health concern and a leading cause of death in the United States and around the world.

Therefore, it is important to continue to explore the potential of novel therapeutic targets and combinatorial therapies. Triggering receptor expressed on myeloid cells 2 (TREM2) is a transmembrane receptor of the immunoglobulin superfamily that associates with DNAX activation protein (DAP) 12 and DAP10 to propagate signals within the cell. TREM2 has primarily been recognized for its expression on cells in the monocyte-macrophage lineage, with the majority of work focusing on microglial function in Alzheimer's Disease.

However, expansion of TREM2 research into the field of cancer has revealed that epithelial tumor cells as well as intratumoral macrophages and myeloid regulatory cells also express TREM2. In this review, we discuss evidence that TREM2 contributes to tumor suppressing or oncogenic activity when expressed by epithelial tumor cells.

In addition, we discuss the immunosuppressive role of TREM2-expressing intratumoral macrophages, and the therapeutic potential of targeting TREM2 in combination with immune checkpoint therapy.

Overall, the literature reveals TREM2 could be considered a novel therapeutic target for certain types of cancer.

论文信息

作者
Wolf EM、Fingleton B、Hasty AH
单位
Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, United States.United States
文献类型
综述
期刊
Frontiers in oncology2022
原文标识
PubMed 36119485 · DOI 10.3389/fonc.2022.984193