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Transcription levels and prognostic significance of the NFI family members in human cancers

BACKGROUND: The nuclear factor I (NFI) is a family of transcription factors consisting of four distinct but closely related genes, NFIA, NFIB, NFIC and NFIX, which are important in the development of various tissues and organs in mammals. Recent study results have shown that NFI family may play a cr...

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Autores principales: Li, Yuexian, Sun, Cheng, Tan, Yonggang, Li, Lin, Zhang, Heying, Liang, Yusi, Zeng, Juan, Zou, Huawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085295/
https://www.ncbi.nlm.nih.gov/pubmed/32219034
http://dx.doi.org/10.7717/peerj.8816
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author Li, Yuexian
Sun, Cheng
Tan, Yonggang
Li, Lin
Zhang, Heying
Liang, Yusi
Zeng, Juan
Zou, Huawei
author_facet Li, Yuexian
Sun, Cheng
Tan, Yonggang
Li, Lin
Zhang, Heying
Liang, Yusi
Zeng, Juan
Zou, Huawei
author_sort Li, Yuexian
collection PubMed
description BACKGROUND: The nuclear factor I (NFI) is a family of transcription factors consisting of four distinct but closely related genes, NFIA, NFIB, NFIC and NFIX, which are important in the development of various tissues and organs in mammals. Recent study results have shown that NFI family may play a critical role in the progression of various human tumors and have been identified as key tumor suppressors and oncogenes for many cancers. However, the expression levels and distinctive prognostic values of the NFI family remain poorly explored in most cancers. MATERIALS AND METHODS: In the present study, the differences in mRNA expression of the NFI family in various cancers were investigated using the Oncomine and TCGA databases, and the mRNA expression, genetic alteration and DNA methylation of the NFI family members in various cancers were examined using cBioPortal for Cancer Genomics. In addition, the prognostic significance of the NFI family was assessed in multiple cancers using the Kaplan–Meier plotter (KM plotter) and SurvExpress databases. RESULTS: The mRNA expression levels in the NFI family were significantly downregulated in most cancers compared with normal tissues and DNA hypermethylation might downregulate the NFI family expression. Although NFIX expression was not downregulated in kidney, colorectal and prostate cancers. Furthermore, NFIB expression was upregulated in gastric cancer. Further survival analyses based on the KM plotter and SurvExpress databases showed dysregulations of the NFI genes were significantly correlated with survival outcomes in breast, lung, and head and neck cancers. Decreased expression levels of NFIA, NFIB and NFIC were associated with poor overall survival (OS) in head and neck cancer. Low mRNA expression of NFIA and NFIB was significantly associated with OS and first progression in lung adenocarcinoma, but not in lung squamous cell carcinoma. In addition, potential correlations between NFI family members and survival outcomes were also observed in liver, esophageal, kidney and cervical cancer. CONCLUSION: The results from the present study indicated certain members of the NFI family could be promising therapeutic targets and novel prognostic biomarkers for human cancers.
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spelling pubmed-70852952020-03-26 Transcription levels and prognostic significance of the NFI family members in human cancers Li, Yuexian Sun, Cheng Tan, Yonggang Li, Lin Zhang, Heying Liang, Yusi Zeng, Juan Zou, Huawei PeerJ Clinical Trials BACKGROUND: The nuclear factor I (NFI) is a family of transcription factors consisting of four distinct but closely related genes, NFIA, NFIB, NFIC and NFIX, which are important in the development of various tissues and organs in mammals. Recent study results have shown that NFI family may play a critical role in the progression of various human tumors and have been identified as key tumor suppressors and oncogenes for many cancers. However, the expression levels and distinctive prognostic values of the NFI family remain poorly explored in most cancers. MATERIALS AND METHODS: In the present study, the differences in mRNA expression of the NFI family in various cancers were investigated using the Oncomine and TCGA databases, and the mRNA expression, genetic alteration and DNA methylation of the NFI family members in various cancers were examined using cBioPortal for Cancer Genomics. In addition, the prognostic significance of the NFI family was assessed in multiple cancers using the Kaplan–Meier plotter (KM plotter) and SurvExpress databases. RESULTS: The mRNA expression levels in the NFI family were significantly downregulated in most cancers compared with normal tissues and DNA hypermethylation might downregulate the NFI family expression. Although NFIX expression was not downregulated in kidney, colorectal and prostate cancers. Furthermore, NFIB expression was upregulated in gastric cancer. Further survival analyses based on the KM plotter and SurvExpress databases showed dysregulations of the NFI genes were significantly correlated with survival outcomes in breast, lung, and head and neck cancers. Decreased expression levels of NFIA, NFIB and NFIC were associated with poor overall survival (OS) in head and neck cancer. Low mRNA expression of NFIA and NFIB was significantly associated with OS and first progression in lung adenocarcinoma, but not in lung squamous cell carcinoma. In addition, potential correlations between NFI family members and survival outcomes were also observed in liver, esophageal, kidney and cervical cancer. CONCLUSION: The results from the present study indicated certain members of the NFI family could be promising therapeutic targets and novel prognostic biomarkers for human cancers. PeerJ Inc. 2020-03-18 /pmc/articles/PMC7085295/ /pubmed/32219034 http://dx.doi.org/10.7717/peerj.8816 Text en © 2020 Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Clinical Trials
Li, Yuexian
Sun, Cheng
Tan, Yonggang
Li, Lin
Zhang, Heying
Liang, Yusi
Zeng, Juan
Zou, Huawei
Transcription levels and prognostic significance of the NFI family members in human cancers
title Transcription levels and prognostic significance of the NFI family members in human cancers
title_full Transcription levels and prognostic significance of the NFI family members in human cancers
title_fullStr Transcription levels and prognostic significance of the NFI family members in human cancers
title_full_unstemmed Transcription levels and prognostic significance of the NFI family members in human cancers
title_short Transcription levels and prognostic significance of the NFI family members in human cancers
title_sort transcription levels and prognostic significance of the nfi family members in human cancers
topic Clinical Trials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085295/
https://www.ncbi.nlm.nih.gov/pubmed/32219034
http://dx.doi.org/10.7717/peerj.8816
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