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肿瘤相关巨噬细胞的空间密度和分布预测非小细胞肺癌的生存。

Spatial Density and Distribution of Tumor-Associated Macrophages Predict Survival in Non-Small Cell Lung Carcinoma.

机构信息

Max Planck Institute for Heart and Lung Research, German Center for Lung Research (DZL), Cardio-Pulmonary Institute (CPI), Bad Nauheim, Germany.

Institute of Biochemistry I, Faculty of Medicine, Goethe University Frankfurt, Frankfurt, Germany.

出版信息

Cancer Res. 2020 Oct 15;80(20):4414-4425. doi: 10.1158/0008-5472.CAN-20-0069. Epub 2020 Jul 22.

Abstract

The respective antitumoral and protumoral roles of M1 and M2 tumor-associated macrophages (TAM) typify the complexity of macrophage function in cancer. In lung cancer, density and topology of distinct TAM phenotypes at the tumor center (TC) versus the invasive margin (IM) are largely unknown. Here, we investigated TAM subtype density and distribution between TC and IM in human lung cancer and TAM associations with overall survival. Macrophages isolated from adjacent nontumor tissue (NM), the TC (TC-TAM), and the IM (IM-TAM) were analyzed with RNA-sequencing (RNA-seq). Lung tumor tissue microarrays from 104 patient samples were constructed. M1 and M2 TAMs were identified using multiplex immunofluorescence staining and a tumor cell-TAM proximity analysis was performed. RNA-seq identified marked differences among NM, TC-TAM, and IM-TAM. On the basis of a panel of five selected markers (CD68, IL12, CCR7, CD163, and ALOX15), M2 predominance over M1 and M2 proximity to tumor cells was observed, especially at IM. Tumor cell proximity to TAM was linked with tumor cell survival and hypoxia was associated with accumulation of M2 TAM. Notably, lower density of M1 TC-TAM and higher proximity of tumor cells to M2 IM-TAM or lower proximity to M1 IM-TAM were linked with poor survival. In addition, three novel molecules (UBXN4, MFSD12, and ACTR6) from RNA-seq served as potential prognostic markers for lung cancer, and M2 predominance and juxtaposition of M2 TAM near tumor cells were associated with poor survival. Together, our results reveal the marked heterogeneity of TAM populations in different tumor regions, with M2 TAM predominance, particularly at IM. SIGNIFICANCE: This study underlines the significance of the density, spatial distribution, and gene expression of TAM phenotypes as prognostic factors for overall survival in lung cancer. GRAPHICAL ABSTRACT: http://cancerres.aacrjournals.org/content/canres/80/20/4414/F1.large.jpg.

摘要

肿瘤相关巨噬细胞(TAM)中 M1 和 M2 亚群的抗肿瘤和促肿瘤作用,典型地体现了巨噬细胞在癌症中的功能复杂性。在肺癌中,肿瘤中心(TC)与侵袭边缘(IM)之间不同 TAM 表型的密度和拓扑结构在很大程度上是未知的。在这里,我们研究了人类肺癌中 TC 与 IM 之间 TAM 亚型的密度和分布,以及 TAM 与总生存期的关联。从相邻非肿瘤组织(NM)、TC(TC-TAM)和 IM(IM-TAM)分离的巨噬细胞进行 RNA 测序(RNA-seq)分析。构建了来自 104 个患者样本的肺肿瘤组织微阵列。使用多重免疫荧光染色鉴定 M1 和 M2 TAMs,并进行了肿瘤细胞-TAM 邻近分析。RNA-seq 鉴定了 NM、TC-TAM 和 IM-TAM 之间的显著差异。基于一组五个选定的标志物(CD68、IL12、CCR7、CD163 和 ALOX15),观察到 M2 对 M1 的优势以及 M2 与肿瘤细胞的接近程度,特别是在 IM 中。肿瘤细胞与 TAM 的接近程度与肿瘤细胞的存活有关,而缺氧与 M2 TAM 的积累有关。值得注意的是,TC-TAM 中 M1 的密度较低,肿瘤细胞与 M2 IM-TAM 的接近程度较高或与 M1 IM-TAM 的接近程度较低,与预后不良相关。此外,RNA-seq 中的三个新分子(UBXN4、MFSD12 和 ACTR6)可作为肺癌的潜在预后标志物,M2 优势和 M2 TAM 紧邻肿瘤细胞的排列与预后不良相关。总之,我们的研究结果揭示了不同肿瘤区域 TAM 群体的显著异质性,其中 M2 TAM 占优势,特别是在 IM 中。

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