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A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer

BACKGROUND: Accurate evaluation of the response to neoadjuvant chemotherapy (NAC) provides important information about systemic therapies for breast cancer, which implies pharmacological response, prognosis, and guide further therapy. Gene profiles overcome the shortcomings of the relatively limited...

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Autores principales: Wu, Jin, Tian, Yuan, Liu, Wei, Zheng, Hong, Xi, Yuanyin, Yan, Yuzhao, Hu, Ying, Liao, Bin, Wang, Minghao, Tang, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629837/
https://www.ncbi.nlm.nih.gov/pubmed/36341435
http://dx.doi.org/10.3389/fimmu.2022.1035667
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author Wu, Jin
Tian, Yuan
Liu, Wei
Zheng, Hong
Xi, Yuanyin
Yan, Yuzhao
Hu, Ying
Liao, Bin
Wang, Minghao
Tang, Peng
author_facet Wu, Jin
Tian, Yuan
Liu, Wei
Zheng, Hong
Xi, Yuanyin
Yan, Yuzhao
Hu, Ying
Liao, Bin
Wang, Minghao
Tang, Peng
author_sort Wu, Jin
collection PubMed
description BACKGROUND: Accurate evaluation of the response to neoadjuvant chemotherapy (NAC) provides important information about systemic therapies for breast cancer, which implies pharmacological response, prognosis, and guide further therapy. Gene profiles overcome the shortcomings of the relatively limited detection indicators of the classical pathological evaluation criteria and the subjectivity of observation, but are complicated and expensive. Therefore, it is essential to develop a more accurate, repeatable, and economical evaluation approach for neoadjuvant chemotherapy responses. METHODS: We analyzed the transcriptional profiles of chemo-resistant breast cancer cell lines and tumors of chemo-resistant breast cancer patients in the GSE25066 dataset. We preliminarily screened out common significantly differentially expressed genes and constructed a NAC response risk model using LASSO regression and univariate and multivariate analyses. The differences in bioinformatic features of tumor cells, immune characteristics, and prognosis were compared between high and low-risk group. The potential drugs that could reverse chemotherapy resistance in breast cancer were screened by the CMap database. RESULTS: Thirty-six genes were commonly up/down-regulated in both NAC chemo-resistant tumors and cells compared to the sensitive tumors and wild-type cells. Through LASSO regression, we obtained a risk model composed of 12 genes. The risk model divided patients into high and low-risk groups. Univariate and multivariate Cox regression analyses suggested that the risk score is an independent prognostic factor for evaluating NAC response in breast cancer. Tumors in risk groups exhibited significant differences in molecular biological characteristics, tumor-infiltrating lymphocytes, and immunosuppressive molecule expression. Our results suggested that the risk score was also a good prognostic factor for breast cancer. Finally, we screened potential drugs that could reverse chemotherapy resistance in breast cancer. CONCLUSION: A novel 12 gene-signature could be used to predict NAC response and predict prognosis in breast cancer.
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spelling pubmed-96298372022-11-03 A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer Wu, Jin Tian, Yuan Liu, Wei Zheng, Hong Xi, Yuanyin Yan, Yuzhao Hu, Ying Liao, Bin Wang, Minghao Tang, Peng Front Immunol Immunology BACKGROUND: Accurate evaluation of the response to neoadjuvant chemotherapy (NAC) provides important information about systemic therapies for breast cancer, which implies pharmacological response, prognosis, and guide further therapy. Gene profiles overcome the shortcomings of the relatively limited detection indicators of the classical pathological evaluation criteria and the subjectivity of observation, but are complicated and expensive. Therefore, it is essential to develop a more accurate, repeatable, and economical evaluation approach for neoadjuvant chemotherapy responses. METHODS: We analyzed the transcriptional profiles of chemo-resistant breast cancer cell lines and tumors of chemo-resistant breast cancer patients in the GSE25066 dataset. We preliminarily screened out common significantly differentially expressed genes and constructed a NAC response risk model using LASSO regression and univariate and multivariate analyses. The differences in bioinformatic features of tumor cells, immune characteristics, and prognosis were compared between high and low-risk group. The potential drugs that could reverse chemotherapy resistance in breast cancer were screened by the CMap database. RESULTS: Thirty-six genes were commonly up/down-regulated in both NAC chemo-resistant tumors and cells compared to the sensitive tumors and wild-type cells. Through LASSO regression, we obtained a risk model composed of 12 genes. The risk model divided patients into high and low-risk groups. Univariate and multivariate Cox regression analyses suggested that the risk score is an independent prognostic factor for evaluating NAC response in breast cancer. Tumors in risk groups exhibited significant differences in molecular biological characteristics, tumor-infiltrating lymphocytes, and immunosuppressive molecule expression. Our results suggested that the risk score was also a good prognostic factor for breast cancer. Finally, we screened potential drugs that could reverse chemotherapy resistance in breast cancer. CONCLUSION: A novel 12 gene-signature could be used to predict NAC response and predict prognosis in breast cancer. Frontiers Media S.A. 2022-10-19 /pmc/articles/PMC9629837/ /pubmed/36341435 http://dx.doi.org/10.3389/fimmu.2022.1035667 Text en Copyright © 2022 Wu, Tian, Liu, Zheng, Xi, Yan, Hu, Liao, Wang and Tang 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
Wu, Jin
Tian, Yuan
Liu, Wei
Zheng, Hong
Xi, Yuanyin
Yan, Yuzhao
Hu, Ying
Liao, Bin
Wang, Minghao
Tang, Peng
A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title_full A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title_fullStr A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title_full_unstemmed A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title_short A novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
title_sort novel twelve-gene signature to predict neoadjuvant chemotherapy response and prognosis in breast cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629837/
https://www.ncbi.nlm.nih.gov/pubmed/36341435
http://dx.doi.org/10.3389/fimmu.2022.1035667
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