Clinical implications and immune implications features of TARS1 in breast cancer

BackgroundThere has been an increase in the number of women suffering from breast cancer in recent years, and discovering new therapeutic targets and efficacy predictive markers is critical for comprehensive breast cancer treatment.MethodsFirst, we used bioinformatics methods to analyze TARS1(encodi...

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Main Authors: Zhengwei Gui, Piao Liu, Dong Zhang, Wanju Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1207867/full
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author Zhengwei Gui
Zhengwei Gui
Piao Liu
Dong Zhang
Wanju Wang
author_facet Zhengwei Gui
Zhengwei Gui
Piao Liu
Dong Zhang
Wanju Wang
author_sort Zhengwei Gui
collection DOAJ
description BackgroundThere has been an increase in the number of women suffering from breast cancer in recent years, and discovering new therapeutic targets and efficacy predictive markers is critical for comprehensive breast cancer treatment.MethodsFirst, we used bioinformatics methods to analyze TARS1(encoding cytoplasmicthreonyl-tRNA synthetase) expression, prognosis, and clinicopathological characteristics in TCGA database breast cancers, and then we collected breast cancer specimens from our center for validation. TARS1 was then subjected to GSEA (Gene Set Enrichment Analysis) enrichment analysis, GO/KEGG pathway enrichment analysis, and breast cancer immune infiltration characterization. As a last step, we examined TARS1’s effects on breast cancer cell behavior with cellular assays.ResultsThe overexpression of TARS1 has been found in several malignant tumors, including breast cancer, and has been linked to poor prognoses. Breast cancers with large primary tumors and negative hormone receptors are more likely to overexpress TARS1. Overexpression of TARS1 promotes the infiltration of T cells, such as Tregs and Th2s, while inhibiting the infiltration of NK cells and CD8+ T cells, which are anticancer cells in breast cancer. TARS1 was also found to be co-expressed with the majority of immune checkpoint-related genes, and breast cancer with TARS1 overexpression responded better to immunotherapy. By knocking down TARS1, breast cancer cells were prevented from proliferating and invading, as well as exhibiting other malignant biological properties.ConclusionAccording to our study, TARS1 may be an oncogene in breast cancer and may be a biomarker of efficacy or a target of immunotherapy in breast cancer.
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spelling doaj.art-b7fc845d95944794991fce06869c28692023-08-11T17:52:45ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-08-011310.3389/fonc.2023.12078671207867Clinical implications and immune implications features of TARS1 in breast cancerZhengwei Gui0Zhengwei Gui1Piao Liu2Dong Zhang3Wanju Wang4Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaDepartment of Breast and Thyroid Surgery, Tongji Hospital, Wuhan, Hubei, ChinaDepartment of General Surgery, Hubei Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Wuhan, Hubei, ChinaDepartment of General Surgery, Hubei Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Wuhan, Hubei, ChinaDepartment of General Surgery, Hubei Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Wuhan, Hubei, ChinaBackgroundThere has been an increase in the number of women suffering from breast cancer in recent years, and discovering new therapeutic targets and efficacy predictive markers is critical for comprehensive breast cancer treatment.MethodsFirst, we used bioinformatics methods to analyze TARS1(encoding cytoplasmicthreonyl-tRNA synthetase) expression, prognosis, and clinicopathological characteristics in TCGA database breast cancers, and then we collected breast cancer specimens from our center for validation. TARS1 was then subjected to GSEA (Gene Set Enrichment Analysis) enrichment analysis, GO/KEGG pathway enrichment analysis, and breast cancer immune infiltration characterization. As a last step, we examined TARS1’s effects on breast cancer cell behavior with cellular assays.ResultsThe overexpression of TARS1 has been found in several malignant tumors, including breast cancer, and has been linked to poor prognoses. Breast cancers with large primary tumors and negative hormone receptors are more likely to overexpress TARS1. Overexpression of TARS1 promotes the infiltration of T cells, such as Tregs and Th2s, while inhibiting the infiltration of NK cells and CD8+ T cells, which are anticancer cells in breast cancer. TARS1 was also found to be co-expressed with the majority of immune checkpoint-related genes, and breast cancer with TARS1 overexpression responded better to immunotherapy. By knocking down TARS1, breast cancer cells were prevented from proliferating and invading, as well as exhibiting other malignant biological properties.ConclusionAccording to our study, TARS1 may be an oncogene in breast cancer and may be a biomarker of efficacy or a target of immunotherapy in breast cancer.https://www.frontiersin.org/articles/10.3389/fonc.2023.1207867/fullTARS1breast cancercell proliferationimmune infiltrationclinical feature
spellingShingle Zhengwei Gui
Zhengwei Gui
Piao Liu
Dong Zhang
Wanju Wang
Clinical implications and immune implications features of TARS1 in breast cancer
Frontiers in Oncology
TARS1
breast cancer
cell proliferation
immune infiltration
clinical feature
title Clinical implications and immune implications features of TARS1 in breast cancer
title_full Clinical implications and immune implications features of TARS1 in breast cancer
title_fullStr Clinical implications and immune implications features of TARS1 in breast cancer
title_full_unstemmed Clinical implications and immune implications features of TARS1 in breast cancer
title_short Clinical implications and immune implications features of TARS1 in breast cancer
title_sort clinical implications and immune implications features of tars1 in breast cancer
topic TARS1
breast cancer
cell proliferation
immune infiltration
clinical feature
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1207867/full
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