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The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer

PURPOSE: Triple-negative breast cancer (TNBC) is a type of breast cancer (BC) showing a high recurrence ratio and a low survival probability, which requires novel actionable molecular targets. The involvement of alternative splicing (AS) in TNBC promoted us to study the potential roles of AS events...

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Autores principales: Wu, Sijia, Wang, Jiachen, Zhu, Xinchao, Chyr, Jacqueline, Zhou, Xiaobo, Wu, Xiaoming, Huang, Liyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841428/
https://www.ncbi.nlm.nih.gov/pubmed/33519909
http://dx.doi.org/10.3389/fgene.2020.604262
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author Wu, Sijia
Wang, Jiachen
Zhu, Xinchao
Chyr, Jacqueline
Zhou, Xiaobo
Wu, Xiaoming
Huang, Liyu
author_facet Wu, Sijia
Wang, Jiachen
Zhu, Xinchao
Chyr, Jacqueline
Zhou, Xiaobo
Wu, Xiaoming
Huang, Liyu
author_sort Wu, Sijia
collection PubMed
description PURPOSE: Triple-negative breast cancer (TNBC) is a type of breast cancer (BC) showing a high recurrence ratio and a low survival probability, which requires novel actionable molecular targets. The involvement of alternative splicing (AS) in TNBC promoted us to study the potential roles of AS events in the survival prognosis of TNBC patients. METHODS: A total of 150 TNBC patients from The Cancer Genome Atlas (TCGA) were involved in this work. To study the effects of AS in the recurrence-free survival (RFS) prognosis of TNBC, we performed the analyses as follows. First, univariate Cox regression model was applied to identify RFS-related AS events. Their host genes were analyzed by Metascape to discover the potential functions and involved pathways. Next, least absolute shrinkage and selection operator (LASSO) method was used to select the most informative RFS-related AS events to constitute an AS risk factor for RFS prognosis, which was evaluated by Kaplan–Meier (KM) and receiver operating characteristic (ROC) curves in all the data and also in different clinical subgroups. Furthermore, we analyzed the relationships between splicing factors (SFs) and these RFS-related AS events to seek the possibility that SFs regulated AS events to influence RFS. Then, we evaluated the potential of these RFS-related AS events in the overall survival (OS) prognosis from all the above aspects. RESULTS: We identified a total of 546 RFS-related AS events, which were enriched in some splicing and TNBC-associated pathways. Among them, seven RFS-related events were integrated into a risk factor, exhibiting satisfactory RFS prognosis alone and even better performance when combined with clinical tumor–node–metastasis stages. Furthermore, the correlation analysis between SFs and the seven AS events revealed the hypotheses that SRPK3 might upregulate PCYT2_44231_AA to have an effect on RFS prognosis and that three other SFs may work together to downregulate FLAD1_7874_RI to influence RFS prognosis. In addition, the seven RFS-related AS events were validated to be promising in the OS prognosis of TNBC as well. CONCLUSION: The abnormal AS events regulated by SFs may act as a kind of biomarker for the survival prognosis of TNBC.
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spelling pubmed-78414282021-01-29 The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer Wu, Sijia Wang, Jiachen Zhu, Xinchao Chyr, Jacqueline Zhou, Xiaobo Wu, Xiaoming Huang, Liyu Front Genet Genetics PURPOSE: Triple-negative breast cancer (TNBC) is a type of breast cancer (BC) showing a high recurrence ratio and a low survival probability, which requires novel actionable molecular targets. The involvement of alternative splicing (AS) in TNBC promoted us to study the potential roles of AS events in the survival prognosis of TNBC patients. METHODS: A total of 150 TNBC patients from The Cancer Genome Atlas (TCGA) were involved in this work. To study the effects of AS in the recurrence-free survival (RFS) prognosis of TNBC, we performed the analyses as follows. First, univariate Cox regression model was applied to identify RFS-related AS events. Their host genes were analyzed by Metascape to discover the potential functions and involved pathways. Next, least absolute shrinkage and selection operator (LASSO) method was used to select the most informative RFS-related AS events to constitute an AS risk factor for RFS prognosis, which was evaluated by Kaplan–Meier (KM) and receiver operating characteristic (ROC) curves in all the data and also in different clinical subgroups. Furthermore, we analyzed the relationships between splicing factors (SFs) and these RFS-related AS events to seek the possibility that SFs regulated AS events to influence RFS. Then, we evaluated the potential of these RFS-related AS events in the overall survival (OS) prognosis from all the above aspects. RESULTS: We identified a total of 546 RFS-related AS events, which were enriched in some splicing and TNBC-associated pathways. Among them, seven RFS-related events were integrated into a risk factor, exhibiting satisfactory RFS prognosis alone and even better performance when combined with clinical tumor–node–metastasis stages. Furthermore, the correlation analysis between SFs and the seven AS events revealed the hypotheses that SRPK3 might upregulate PCYT2_44231_AA to have an effect on RFS prognosis and that three other SFs may work together to downregulate FLAD1_7874_RI to influence RFS prognosis. In addition, the seven RFS-related AS events were validated to be promising in the OS prognosis of TNBC as well. CONCLUSION: The abnormal AS events regulated by SFs may act as a kind of biomarker for the survival prognosis of TNBC. Frontiers Media S.A. 2021-01-14 /pmc/articles/PMC7841428/ /pubmed/33519909 http://dx.doi.org/10.3389/fgene.2020.604262 Text en Copyright © 2021 Wu, Wang, Zhu, Chyr, Zhou, Wu and Huang. http://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 Genetics
Wu, Sijia
Wang, Jiachen
Zhu, Xinchao
Chyr, Jacqueline
Zhou, Xiaobo
Wu, Xiaoming
Huang, Liyu
The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title_full The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title_fullStr The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title_full_unstemmed The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title_short The Functional Impact of Alternative Splicing on the Survival Prognosis of Triple-Negative Breast Cancer
title_sort functional impact of alternative splicing on the survival prognosis of triple-negative breast cancer
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841428/
https://www.ncbi.nlm.nih.gov/pubmed/33519909
http://dx.doi.org/10.3389/fgene.2020.604262
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