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Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer

Tertiary lymphoid structures (TLSs) play a crucial role in determining prognosis and response to immunotherapy in several solid malignancies. Nevertheless, the effect of TLS-associated gene signature based on The Cancer Genome Atlas (TCGA) cohort in patients with breast cancer (BRCA) remains controv...

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Autores principales: Wang, Liye, Gong, Shuai, Pang, Lina, Zhang, Shengli, Zhang, Xiaoke, He, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439954/
https://www.ncbi.nlm.nih.gov/pubmed/37598257
http://dx.doi.org/10.1038/s41598-023-40042-7
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author Wang, Liye
Gong, Shuai
Pang, Lina
Zhang, Shengli
Zhang, Xiaoke
He, Wei
author_facet Wang, Liye
Gong, Shuai
Pang, Lina
Zhang, Shengli
Zhang, Xiaoke
He, Wei
author_sort Wang, Liye
collection PubMed
description Tertiary lymphoid structures (TLSs) play a crucial role in determining prognosis and response to immunotherapy in several solid malignancies. Nevertheless, the effect of TLS-associated gene signature based on The Cancer Genome Atlas (TCGA) cohort in patients with breast cancer (BRCA) remains controversial. Based on TCGA-BRCA dataset (n = 866), 9-gene was identified to construct an TLS signature and further analyzed its prognostic value. Then, we explored the relationship of this TLS signature with molecular subtype, immune microenvironment, tumor mutational burden (TMB). High-TLS signature patients had a better overall survival (OS) than low-TLS signature patients, consistent with the results in the METABRIC cohort. Multivariate analysis revealed that TLS signature remained an independent prognostic indicator for OS. In addition, we established a nomogram with the integration of TLS signature and other independent variables to predict individual risk of death. The comprehensive results showed that patients with high TLS signature benefit from immunotherapy; the signature was also correlated with inhibition of cell proliferation pathways, low TP53 mutation rate, high infiltration of B cells, CD8 + T cells, CD4 + T cells, and M1 macrophages. Therefore, TLS signature is a promising biomarker to distinguish the prognosis and immune microenvironment in BRCA.
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spelling pubmed-104399542023-08-21 Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer Wang, Liye Gong, Shuai Pang, Lina Zhang, Shengli Zhang, Xiaoke He, Wei Sci Rep Article Tertiary lymphoid structures (TLSs) play a crucial role in determining prognosis and response to immunotherapy in several solid malignancies. Nevertheless, the effect of TLS-associated gene signature based on The Cancer Genome Atlas (TCGA) cohort in patients with breast cancer (BRCA) remains controversial. Based on TCGA-BRCA dataset (n = 866), 9-gene was identified to construct an TLS signature and further analyzed its prognostic value. Then, we explored the relationship of this TLS signature with molecular subtype, immune microenvironment, tumor mutational burden (TMB). High-TLS signature patients had a better overall survival (OS) than low-TLS signature patients, consistent with the results in the METABRIC cohort. Multivariate analysis revealed that TLS signature remained an independent prognostic indicator for OS. In addition, we established a nomogram with the integration of TLS signature and other independent variables to predict individual risk of death. The comprehensive results showed that patients with high TLS signature benefit from immunotherapy; the signature was also correlated with inhibition of cell proliferation pathways, low TP53 mutation rate, high infiltration of B cells, CD8 + T cells, CD4 + T cells, and M1 macrophages. Therefore, TLS signature is a promising biomarker to distinguish the prognosis and immune microenvironment in BRCA. Nature Publishing Group UK 2023-08-19 /pmc/articles/PMC10439954/ /pubmed/37598257 http://dx.doi.org/10.1038/s41598-023-40042-7 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/) .
spellingShingle Article
Wang, Liye
Gong, Shuai
Pang, Lina
Zhang, Shengli
Zhang, Xiaoke
He, Wei
Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title_full Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title_fullStr Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title_full_unstemmed Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title_short Genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
title_sort genomic properties and clinical outcomes associated with tertiary lymphoid structures in patients with breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439954/
https://www.ncbi.nlm.nih.gov/pubmed/37598257
http://dx.doi.org/10.1038/s41598-023-40042-7
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