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Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer

BACKGROUND: Breast cancer presents as one of the top health threats to women around the world. Myeloid cells are the most abundant cells and the major immune coordinator in breast cancer tumor microenvironment (TME), target therapies that harness the anti-tumor potential of myeloid cells are current...

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Autores principales: Yang, Chenxuan, Liu, Jiaxiang, Zhao, Shuangtao, Shang, Qingyao, Ren, Fei, Feng, Kexin, Zhang, Ruixuan, Kang, Xiyu, Wang, Xin, Wang, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246424/
https://www.ncbi.nlm.nih.gov/pubmed/37287069
http://dx.doi.org/10.1186/s13058-023-01669-6
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author Yang, Chenxuan
Liu, Jiaxiang
Zhao, Shuangtao
Shang, Qingyao
Ren, Fei
Feng, Kexin
Zhang, Ruixuan
Kang, Xiyu
Wang, Xin
Wang, Xiang
author_facet Yang, Chenxuan
Liu, Jiaxiang
Zhao, Shuangtao
Shang, Qingyao
Ren, Fei
Feng, Kexin
Zhang, Ruixuan
Kang, Xiyu
Wang, Xin
Wang, Xiang
author_sort Yang, Chenxuan
collection PubMed
description BACKGROUND: Breast cancer presents as one of the top health threats to women around the world. Myeloid cells are the most abundant cells and the major immune coordinator in breast cancer tumor microenvironment (TME), target therapies that harness the anti-tumor potential of myeloid cells are currently being evaluated in clinical trials. However, the landscape and dynamic transition of myeloid cells in breast cancer TME are still largely unknown. METHODS: Myeloid cells were characterized in the single-cell data and extracted with a deconvolution algorithm to be assessed in bulk-sequencing data. We used the Shannon index to describe the diversity of infiltrating myeloid cells. A 5-gene surrogate scoring system was then constructed and evaluated to infer the myeloid cell diversity in a clinically feasible manner. RESULTS: We dissected the breast cancer infiltrating myeloid cells into 15 subgroups including macrophages, dendritic cells (DCs), and monocytes. Mac_CCL4 had the highest angiogenic activity, Mac_APOE and Mac_CXCL10 were highly active in cytokine secretion, and the DCs had upregulated antigen presentation pathways. The infiltrating myeloid diversity was calculated in the deconvoluted bulk-sequencing data, and we found that higher myeloid diversity was robustly associated with more favorable clinical outcomes, higher neoadjuvant therapy responses, and a higher rate of somatic mutations. We then used machine learning methods to perform feature selection and reduction, which generated a clinical-friendly scoring system consisting of 5 genes (C3, CD27, GFPT2, GMFG, and HLA-DPB1) that could be used to predict clinical outcomes in breast cancer patients. CONCLUSIONS: Our study explored the heterogeneity and plasticity of breast cancer infiltrating myeloid cells. By using a novel combination of bioinformatic approaches, we proposed the myeloid diversity index as a new prognostic metric and constructed a clinically practical scoring system to guide future patient evaluation and risk stratification. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-023-01669-6.
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spelling pubmed-102464242023-06-08 Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer Yang, Chenxuan Liu, Jiaxiang Zhao, Shuangtao Shang, Qingyao Ren, Fei Feng, Kexin Zhang, Ruixuan Kang, Xiyu Wang, Xin Wang, Xiang Breast Cancer Res Research BACKGROUND: Breast cancer presents as one of the top health threats to women around the world. Myeloid cells are the most abundant cells and the major immune coordinator in breast cancer tumor microenvironment (TME), target therapies that harness the anti-tumor potential of myeloid cells are currently being evaluated in clinical trials. However, the landscape and dynamic transition of myeloid cells in breast cancer TME are still largely unknown. METHODS: Myeloid cells were characterized in the single-cell data and extracted with a deconvolution algorithm to be assessed in bulk-sequencing data. We used the Shannon index to describe the diversity of infiltrating myeloid cells. A 5-gene surrogate scoring system was then constructed and evaluated to infer the myeloid cell diversity in a clinically feasible manner. RESULTS: We dissected the breast cancer infiltrating myeloid cells into 15 subgroups including macrophages, dendritic cells (DCs), and monocytes. Mac_CCL4 had the highest angiogenic activity, Mac_APOE and Mac_CXCL10 were highly active in cytokine secretion, and the DCs had upregulated antigen presentation pathways. The infiltrating myeloid diversity was calculated in the deconvoluted bulk-sequencing data, and we found that higher myeloid diversity was robustly associated with more favorable clinical outcomes, higher neoadjuvant therapy responses, and a higher rate of somatic mutations. We then used machine learning methods to perform feature selection and reduction, which generated a clinical-friendly scoring system consisting of 5 genes (C3, CD27, GFPT2, GMFG, and HLA-DPB1) that could be used to predict clinical outcomes in breast cancer patients. CONCLUSIONS: Our study explored the heterogeneity and plasticity of breast cancer infiltrating myeloid cells. By using a novel combination of bioinformatic approaches, we proposed the myeloid diversity index as a new prognostic metric and constructed a clinically practical scoring system to guide future patient evaluation and risk stratification. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13058-023-01669-6. BioMed Central 2023-06-07 2023 /pmc/articles/PMC10246424/ /pubmed/37287069 http://dx.doi.org/10.1186/s13058-023-01669-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Chenxuan
Liu, Jiaxiang
Zhao, Shuangtao
Shang, Qingyao
Ren, Fei
Feng, Kexin
Zhang, Ruixuan
Kang, Xiyu
Wang, Xin
Wang, Xiang
Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title_full Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title_fullStr Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title_full_unstemmed Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title_short Infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
title_sort infiltrating myeloid cell diversity determines oncological characteristics and clinical outcomes in breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246424/
https://www.ncbi.nlm.nih.gov/pubmed/37287069
http://dx.doi.org/10.1186/s13058-023-01669-6
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