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Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma

Global efforts have been undertaken to define the genome‐wide distribution of epigenetic markers in cancerous tissues, which provide an invaluable opportunity to understand cancer biology and identify predictive signatures. Several studies have focused on the gene expression patterns of squamous car...

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Autores principales: Yang, Jingrun, Xie, Kuixia, Wang, Zihui, Li, Chengxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396437/
https://www.ncbi.nlm.nih.gov/pubmed/32536035
http://dx.doi.org/10.1002/2211-5463.12912
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author Yang, Jingrun
Xie, Kuixia
Wang, Zihui
Li, Chengxin
author_facet Yang, Jingrun
Xie, Kuixia
Wang, Zihui
Li, Chengxin
author_sort Yang, Jingrun
collection PubMed
description Global efforts have been undertaken to define the genome‐wide distribution of epigenetic markers in cancerous tissues, which provide an invaluable opportunity to understand cancer biology and identify predictive signatures. Several studies have focused on the gene expression patterns of squamous carcinoma to identify tumor subtypes and find prognostic and therapeutic targets because squamous carcinoma genomes showed high instability. However, the number of reliable reports referring prognostic significance of genes and their role in squamous carcinoma is still quite limited. Krüppel‐like factor 7 (KLF7) is a transcription factor that is widely expressed in numerous human tissues at low levels. Members of the KLF family have established roles in tumor cell fate, stress response, cell survival and the tumor‐initiating properties of cancer stem‐like cells. Hence to investigate whether KFL7 expression from cancer tissue holds promise as a prognostic and/or therapeutic target, we analyzed gene expression profiles from squamous carcinoma and surgical margin tissues in The Cancer Genome Atlas. We identified significant up‐regulation of KLF7 in squamous carcinoma, which was confirmed by immunohistochemical staining. Elevated KLF7 expression was associated with poor squamous carcinoma prognosis before and after correcting for confounding factors by multivariate Cox regression analysis. Several pathways, such as Neurotrophin and GnRH pathways, were activated in KLF7‐up‐regulated squamous carcinoma samples through Gene Set Enrichment Analysis. In conclusion, we consolidate the potential role(s) of KLF7 in squamous carcinoma carcinogenesis from The Cancer Genome Atlas surgical margin tissue, offering insights into expression signatures that are potentially useful for prognosis modalities.
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spelling pubmed-73964372020-08-06 Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma Yang, Jingrun Xie, Kuixia Wang, Zihui Li, Chengxin FEBS Open Bio Research Articles Global efforts have been undertaken to define the genome‐wide distribution of epigenetic markers in cancerous tissues, which provide an invaluable opportunity to understand cancer biology and identify predictive signatures. Several studies have focused on the gene expression patterns of squamous carcinoma to identify tumor subtypes and find prognostic and therapeutic targets because squamous carcinoma genomes showed high instability. However, the number of reliable reports referring prognostic significance of genes and their role in squamous carcinoma is still quite limited. Krüppel‐like factor 7 (KLF7) is a transcription factor that is widely expressed in numerous human tissues at low levels. Members of the KLF family have established roles in tumor cell fate, stress response, cell survival and the tumor‐initiating properties of cancer stem‐like cells. Hence to investigate whether KFL7 expression from cancer tissue holds promise as a prognostic and/or therapeutic target, we analyzed gene expression profiles from squamous carcinoma and surgical margin tissues in The Cancer Genome Atlas. We identified significant up‐regulation of KLF7 in squamous carcinoma, which was confirmed by immunohistochemical staining. Elevated KLF7 expression was associated with poor squamous carcinoma prognosis before and after correcting for confounding factors by multivariate Cox regression analysis. Several pathways, such as Neurotrophin and GnRH pathways, were activated in KLF7‐up‐regulated squamous carcinoma samples through Gene Set Enrichment Analysis. In conclusion, we consolidate the potential role(s) of KLF7 in squamous carcinoma carcinogenesis from The Cancer Genome Atlas surgical margin tissue, offering insights into expression signatures that are potentially useful for prognosis modalities. John Wiley and Sons Inc. 2020-07-13 /pmc/articles/PMC7396437/ /pubmed/32536035 http://dx.doi.org/10.1002/2211-5463.12912 Text en © 2020 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yang, Jingrun
Xie, Kuixia
Wang, Zihui
Li, Chengxin
Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title_full Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title_fullStr Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title_full_unstemmed Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title_short Elevated KLF7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
title_sort elevated klf7 levels may serve as a prognostic signature and might contribute to progression of squamous carcinoma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396437/
https://www.ncbi.nlm.nih.gov/pubmed/32536035
http://dx.doi.org/10.1002/2211-5463.12912
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