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Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer
BACKGROUND: Natural killer (NK) cells are crucial to the emergence, identification, and prognosis of cancers. The roles of NK cell-related genes in the tumor immune microenvironment (TIME) and immunotherapy treatment are unclear. Triple-negative breast cancer (TNBC) is a highly aggressive malignant...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373504/ https://www.ncbi.nlm.nih.gov/pubmed/37520534 http://dx.doi.org/10.3389/fimmu.2023.1200282 |
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author | Liu, Zundong Ding, Mingji Qiu, Pengjun Pan, Kelun Guo, Qiaonan |
author_facet | Liu, Zundong Ding, Mingji Qiu, Pengjun Pan, Kelun Guo, Qiaonan |
author_sort | Liu, Zundong |
collection | PubMed |
description | BACKGROUND: Natural killer (NK) cells are crucial to the emergence, identification, and prognosis of cancers. The roles of NK cell-related genes in the tumor immune microenvironment (TIME) and immunotherapy treatment are unclear. Triple-negative breast cancer (TNBC) is a highly aggressive malignant tumor. Hence, this study was conducted to develop a reliable risk model related to NK cells and provide a novel system for predicting the prognosis of TNBC. METHODS: NK cell-related genes were collected from previous studies. Based on TCGA and GEO database, univariate and LASSO cox regression analysis were used to establish the NK cell-related gene signature. The patients with TNBC were separated to high-risk and low-risk groups. After that, survival analysis was conducted and the responses to immunotherapies were evaluated on the basis of the signature. Moreover, the drug sensitivity of some traditional chemotherapeutic drugs was assessed by using the “oncoPredict” R package. In addition, the expression levels of the genes involved in the signature were validated by using qRT-PCR in TNBC cell lines. RESULTS: The patients with TNBC were divided into high- and low-risk groups according to the median risk score of the 5-NK cell-related gene signature. The low-risk group was associated with a better clinical outcome. Besides, the differentially expressed genes between the different risk groups were enriched in the biological activities associated with immunity. The tumor immune cells were found to be highly infiltrated in the low-risk groups. In accordance with the TIDE score and immune checkpoint-related gene expression analysis, TNBC patients in the low-risk groups were suggested to have better responses to immunotherapies. Eventually, some classical anti-tumor drugs were shown to be less effective in high-risk groups than in low-risk groups. CONCLUSION: The 5-NK cell-related gene signature exhibit outstanding predictive performance and provide fresh viewpoints for evaluating the success of immunotherapy. It will provide new insights to achieve precision and integrated treatment for TNBC in the future. |
format | Online Article Text |
id | pubmed-10373504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103735042023-07-28 Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer Liu, Zundong Ding, Mingji Qiu, Pengjun Pan, Kelun Guo, Qiaonan Front Immunol Immunology BACKGROUND: Natural killer (NK) cells are crucial to the emergence, identification, and prognosis of cancers. The roles of NK cell-related genes in the tumor immune microenvironment (TIME) and immunotherapy treatment are unclear. Triple-negative breast cancer (TNBC) is a highly aggressive malignant tumor. Hence, this study was conducted to develop a reliable risk model related to NK cells and provide a novel system for predicting the prognosis of TNBC. METHODS: NK cell-related genes were collected from previous studies. Based on TCGA and GEO database, univariate and LASSO cox regression analysis were used to establish the NK cell-related gene signature. The patients with TNBC were separated to high-risk and low-risk groups. After that, survival analysis was conducted and the responses to immunotherapies were evaluated on the basis of the signature. Moreover, the drug sensitivity of some traditional chemotherapeutic drugs was assessed by using the “oncoPredict” R package. In addition, the expression levels of the genes involved in the signature were validated by using qRT-PCR in TNBC cell lines. RESULTS: The patients with TNBC were divided into high- and low-risk groups according to the median risk score of the 5-NK cell-related gene signature. The low-risk group was associated with a better clinical outcome. Besides, the differentially expressed genes between the different risk groups were enriched in the biological activities associated with immunity. The tumor immune cells were found to be highly infiltrated in the low-risk groups. In accordance with the TIDE score and immune checkpoint-related gene expression analysis, TNBC patients in the low-risk groups were suggested to have better responses to immunotherapies. Eventually, some classical anti-tumor drugs were shown to be less effective in high-risk groups than in low-risk groups. CONCLUSION: The 5-NK cell-related gene signature exhibit outstanding predictive performance and provide fresh viewpoints for evaluating the success of immunotherapy. It will provide new insights to achieve precision and integrated treatment for TNBC in the future. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10373504/ /pubmed/37520534 http://dx.doi.org/10.3389/fimmu.2023.1200282 Text en Copyright © 2023 Liu, Ding, Qiu, Pan and Guo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Liu, Zundong Ding, Mingji Qiu, Pengjun Pan, Kelun Guo, Qiaonan Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title | Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title_full | Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title_fullStr | Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title_full_unstemmed | Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title_short | Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
title_sort | natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373504/ https://www.ncbi.nlm.nih.gov/pubmed/37520534 http://dx.doi.org/10.3389/fimmu.2023.1200282 |
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