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Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia

Despite advances in early diagnosis and treatment, cancer remains the major reason for mortality worldwide. The Runt-related transcription factor (RUNX) family has been reported to participate in diverse human diseases. However, little is known about their expression and prognostic values in human l...

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Autores principales: Sun, Cheng-Cao, Li, Shu-Jun, Chen, Zhen-Long, Li, Guang, Zhang, Qian, Li, De-Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350111/
https://www.ncbi.nlm.nih.gov/pubmed/30719500
http://dx.doi.org/10.1016/j.omto.2018.12.008
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author Sun, Cheng-Cao
Li, Shu-Jun
Chen, Zhen-Long
Li, Guang
Zhang, Qian
Li, De-Jia
author_facet Sun, Cheng-Cao
Li, Shu-Jun
Chen, Zhen-Long
Li, Guang
Zhang, Qian
Li, De-Jia
author_sort Sun, Cheng-Cao
collection PubMed
description Despite advances in early diagnosis and treatment, cancer remains the major reason for mortality worldwide. The Runt-related transcription factor (RUNX) family has been reported to participate in diverse human diseases. However, little is known about their expression and prognostic values in human leukemia. Herein, we conducted a detailed cancer versus normal analysis. The mRNA expression levels of the RUNX family in various kinds of cancers, including leukemia, were analyzed via the ONCOMINE and GEPIA (Gene Expression Profiling Interactive Analysis) databases. We observed that the mRNA expression levels of RUNX1, RUNX2, and RUNX3 were all increased in most cancers compared with normal tissues, especially in leukemia. Moreover, the expression levels of RUNX1, RUNX2, and RUNX3 are also highly expressed in almost all cancer cell lines, particularly in acute myeloid leukemia (AML) cell lines, analyzed by Cancer Cell Line Encyclopedia (CCLE) and European Bioinformatics Institute (EMBL-EBI) databases. Further, the LinkedOmics and GEPIA databases were used to evaluate the prognostic values. In survival analyses based on LinkedOmics, higher expression of RUNX1 and RUNX2 indicated a better overall survival (OS), but with no significance, whereas increased RUNX3 revealed a poor OS in leukemia. In addition, the GEPIA dataset was also used to perform survival analyses, and results manifested that the expression of RUNX1 and RUNX2 had no remarkable correction with OS in leukemia, but it showed highly expressed RUNX3 was significantly related with poor OS in leukemia. In conclusion, the RUNX family showed significant expression differences between cancer and normal tissues, especially leukemia, and RUNX3 could be a promising prognostic biomarker for leukemia.
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spelling pubmed-63501112019-02-04 Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia Sun, Cheng-Cao Li, Shu-Jun Chen, Zhen-Long Li, Guang Zhang, Qian Li, De-Jia Mol Ther Oncolytics Article Despite advances in early diagnosis and treatment, cancer remains the major reason for mortality worldwide. The Runt-related transcription factor (RUNX) family has been reported to participate in diverse human diseases. However, little is known about their expression and prognostic values in human leukemia. Herein, we conducted a detailed cancer versus normal analysis. The mRNA expression levels of the RUNX family in various kinds of cancers, including leukemia, were analyzed via the ONCOMINE and GEPIA (Gene Expression Profiling Interactive Analysis) databases. We observed that the mRNA expression levels of RUNX1, RUNX2, and RUNX3 were all increased in most cancers compared with normal tissues, especially in leukemia. Moreover, the expression levels of RUNX1, RUNX2, and RUNX3 are also highly expressed in almost all cancer cell lines, particularly in acute myeloid leukemia (AML) cell lines, analyzed by Cancer Cell Line Encyclopedia (CCLE) and European Bioinformatics Institute (EMBL-EBI) databases. Further, the LinkedOmics and GEPIA databases were used to evaluate the prognostic values. In survival analyses based on LinkedOmics, higher expression of RUNX1 and RUNX2 indicated a better overall survival (OS), but with no significance, whereas increased RUNX3 revealed a poor OS in leukemia. In addition, the GEPIA dataset was also used to perform survival analyses, and results manifested that the expression of RUNX1 and RUNX2 had no remarkable correction with OS in leukemia, but it showed highly expressed RUNX3 was significantly related with poor OS in leukemia. In conclusion, the RUNX family showed significant expression differences between cancer and normal tissues, especially leukemia, and RUNX3 could be a promising prognostic biomarker for leukemia. American Society of Gene & Cell Therapy 2018-12-18 /pmc/articles/PMC6350111/ /pubmed/30719500 http://dx.doi.org/10.1016/j.omto.2018.12.008 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sun, Cheng-Cao
Li, Shu-Jun
Chen, Zhen-Long
Li, Guang
Zhang, Qian
Li, De-Jia
Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title_full Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title_fullStr Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title_full_unstemmed Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title_short Expression and Prognosis Analyses of Runt-Related Transcription Factor Family in Human Leukemia
title_sort expression and prognosis analyses of runt-related transcription factor family in human leukemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350111/
https://www.ncbi.nlm.nih.gov/pubmed/30719500
http://dx.doi.org/10.1016/j.omto.2018.12.008
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