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综合分析揭示了三阴性乳腺癌中基于肿瘤相关巨噬细胞的风险特征的预后相关性和免疫特征。

Integrated analysis reveals prognostic correlation and immune characteristics of a tumor-associated macrophage-based risk signature in triple-negative breast cancer.

作者信息

Miao Shichen, Bian Chengyu, Fang Jun, Wang Shanshan, You Huan, Zhou Yi, Ni Qichao

机构信息

Department of Thyroid and Breast Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.

Department of Thoracic Surgery, The First People's Hospital of Changzhou and The Third Affiliated Hospital of Soochow University, Changzhou, China.

出版信息

Transl Cancer Res. 2024 Oct 31;13(10):5214-5232. doi: 10.21037/tcr-24-1037. Epub 2024 Oct 29.

DOI:10.21037/tcr-24-1037
PMID:39525038
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11543029/
Abstract

BACKGROUND

Tumor-associated macrophages play a critical role in the progression and immune response of triple-negative breast cancer (TNBC). Our study aimed to explore the characteristics of tumor-associated macrophages (TAMs) in TNBC, construct a risk signature associated with TAM clusters, and verify its relationship with prognosis and immune-related characteristics.

METHODS

Firstly, we identified four TAM clusters and determined prognosis-related clusters in TNBC based on the single-cell RNA sequencing (scRNA-seq) data. Subsequently, the TAM-related prognostic genes were obtained by the univariate Cox regression analysis and an 8-gene risk signature was then constructed by least absolute shrinkage and selection operator (LASSO) regression based on these TAM-related prognostic genes. Analyses of immune characteristics showed a significant association between the signature with stromal and immune scores, as well as some immune cells.

RESULTS

Multivariate analysis revealed that the risk signature was an independent prognostic factor for TNBC, and its value in predicting immunotherapeutic outcomes was also confirmed. A novel nomogram integrating the stage and TAM-based risk signature was constructed, which exhibited favorable predictability and reliability in the prognosis prediction of TNBC. Finally, the increasing expression of which is one of the eight hub genes was explored in TNBC by experiments including reverse-transcriptase polymerase chain reaction, western blot, and immunohistochemistry.

CONCLUSIONS

Our study may provide unique insights into obtaining independent prognostic factors, improving immunotherapeutic strategies, and identifying effective therapeutic targets for TNBC.

摘要

背景

肿瘤相关巨噬细胞在三阴性乳腺癌(TNBC)的进展和免疫反应中起关键作用。我们的研究旨在探讨TNBC中肿瘤相关巨噬细胞(TAM)的特征,构建与TAM簇相关的风险特征,并验证其与预后和免疫相关特征的关系。

方法

首先,我们基于单细胞RNA测序(scRNA-seq)数据在TNBC中鉴定了四个TAM簇并确定了与预后相关的簇。随后,通过单变量Cox回归分析获得TAM相关的预后基因,然后基于这些TAM相关的预后基因通过最小绝对收缩和选择算子(LASSO)回归构建一个8基因风险特征。免疫特征分析显示该特征与基质和免疫评分以及一些免疫细胞之间存在显著关联。

结果

多变量分析显示该风险特征是TNBC的独立预后因素,其在预测免疫治疗结果中的价值也得到了证实。构建了一个整合分期和基于TAM的风险特征的新型列线图,该列线图在TNBC的预后预测中表现出良好的预测性和可靠性。最后,通过逆转录聚合酶链反应、蛋白质免疫印迹和免疫组织化学等实验,在TNBC中探索了八个枢纽基因之一的表达增加情况。

结论

我们的研究可能为获得独立预后因素、改进免疫治疗策略以及确定TNBC的有效治疗靶点提供独特的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/e9fbe21c8422/tcr-13-10-5214-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/a85614dabc9e/tcr-13-10-5214-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/5e28a5b51c4a/tcr-13-10-5214-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/cfa50dbc7c3d/tcr-13-10-5214-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/aad8ae87091c/tcr-13-10-5214-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/a8466ed726a0/tcr-13-10-5214-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/34fb942fa9aa/tcr-13-10-5214-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/f4f150b9b7b5/tcr-13-10-5214-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/e9fbe21c8422/tcr-13-10-5214-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/a85614dabc9e/tcr-13-10-5214-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/5e28a5b51c4a/tcr-13-10-5214-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/cfa50dbc7c3d/tcr-13-10-5214-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/aad8ae87091c/tcr-13-10-5214-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/a8466ed726a0/tcr-13-10-5214-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/34fb942fa9aa/tcr-13-10-5214-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/f4f150b9b7b5/tcr-13-10-5214-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6772/11543029/e9fbe21c8422/tcr-13-10-5214-f8.jpg

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本文引用的文献

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Cancer Res. 2024 Jul 15;84(14):2282-2296. doi: 10.1158/0008-5472.CAN-23-3429.
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Chemotherapy-elicited extracellular vesicle CXCL1 from dying cells promotes triple-negative breast cancer metastasis by activating TAM/PD-L1 signaling.化疗诱导的来自垂死细胞的细胞外囊泡CXCL1通过激活TAM/PD-L1信号促进三阴性乳腺癌转移。
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Modulation of miR-146b by N6-methyladenosine modification remodels tumor-associated macrophages and enhances anti-PD-1 therapy in colorectal cancer.
N6-甲基腺苷修饰调控 miR-146b 重塑肿瘤相关巨噬细胞,增强结直肠癌抗 PD-1 治疗。
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A fibroblast-associated signature predicts prognosis and immunotherapy in esophageal squamous cell cancer.成纤维细胞相关特征可预测食管鳞癌的预后和免疫治疗反应。
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Aptamer-Based Strategies to Boost Immunotherapy in TNBC.基于适配体的三阴性乳腺癌免疫治疗增强策略
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