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Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum

Colorectal cancer (CRC) is a common and highly lethal form of cancer. Although the etiologic role of Fusobacterium nucleatum (F. nucleatum) in the development of CRC has been elucidated, the specific tumor molecules involved in the progression of CRC induced by F. nucleatum have not been identified....

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Autores principales: Feng, Yu-yang, Zeng, Dong-zhu, Tong, Ya-nan, Lu, Xiao-xue, Dun, Guo-dong, Tang, Bin, Zhang, Zhu-jun, Ye, Xin-li, Li, Qian, Xie, Jian-ping, Mao, Xu-hu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450631/
https://www.ncbi.nlm.nih.gov/pubmed/30951563
http://dx.doi.org/10.1371/journal.pone.0215088
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author Feng, Yu-yang
Zeng, Dong-zhu
Tong, Ya-nan
Lu, Xiao-xue
Dun, Guo-dong
Tang, Bin
Zhang, Zhu-jun
Ye, Xin-li
Li, Qian
Xie, Jian-ping
Mao, Xu-hu
author_facet Feng, Yu-yang
Zeng, Dong-zhu
Tong, Ya-nan
Lu, Xiao-xue
Dun, Guo-dong
Tang, Bin
Zhang, Zhu-jun
Ye, Xin-li
Li, Qian
Xie, Jian-ping
Mao, Xu-hu
author_sort Feng, Yu-yang
collection PubMed
description Colorectal cancer (CRC) is a common and highly lethal form of cancer. Although the etiologic role of Fusobacterium nucleatum (F. nucleatum) in the development of CRC has been elucidated, the specific tumor molecules involved in the progression of CRC induced by F. nucleatum have not been identified. This study investigated several miRNAs and genes involved in the progression of F. nucleatum-induced CRC by Affymetrix miRNA microarray technology and GeneChip Human Transcriptome Array 2.0. The results suggest that miR-4474 and miR-4717 are up-regulated in CRC tissues in response to F. nucleatum infection, compared with the control group (paracancerous tissues), while other genes associated with signaling pathways in cancer, including CREB-binding protein (CREBBP), STAT1, PRKACB, CAMK2B, JUN, TP53 and EWSR1, were dysregulated. Bioinformatic analysis identified CREBBP as the primary aberrantly expressed gene in F. nucleatum-induced CRC. Consistent with the microarray analysis results, real-time RT-PCR analysis demonstrated that the expression of miR-4474/4717 was upregulated while that of CREBBP mRNA was downregulated in CRC patients infected with F. nucleatum. Additionally, CREBBP was identified as a novel target of miR-4474/4717. The results of this study suggest that miR-4474 and miR-4717 are involved in the progression of F. nucleatum-induced CRC by posttranscriptionally regulating the target gene CREBBP.
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spelling pubmed-64506312019-04-19 Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum Feng, Yu-yang Zeng, Dong-zhu Tong, Ya-nan Lu, Xiao-xue Dun, Guo-dong Tang, Bin Zhang, Zhu-jun Ye, Xin-li Li, Qian Xie, Jian-ping Mao, Xu-hu PLoS One Research Article Colorectal cancer (CRC) is a common and highly lethal form of cancer. Although the etiologic role of Fusobacterium nucleatum (F. nucleatum) in the development of CRC has been elucidated, the specific tumor molecules involved in the progression of CRC induced by F. nucleatum have not been identified. This study investigated several miRNAs and genes involved in the progression of F. nucleatum-induced CRC by Affymetrix miRNA microarray technology and GeneChip Human Transcriptome Array 2.0. The results suggest that miR-4474 and miR-4717 are up-regulated in CRC tissues in response to F. nucleatum infection, compared with the control group (paracancerous tissues), while other genes associated with signaling pathways in cancer, including CREB-binding protein (CREBBP), STAT1, PRKACB, CAMK2B, JUN, TP53 and EWSR1, were dysregulated. Bioinformatic analysis identified CREBBP as the primary aberrantly expressed gene in F. nucleatum-induced CRC. Consistent with the microarray analysis results, real-time RT-PCR analysis demonstrated that the expression of miR-4474/4717 was upregulated while that of CREBBP mRNA was downregulated in CRC patients infected with F. nucleatum. Additionally, CREBBP was identified as a novel target of miR-4474/4717. The results of this study suggest that miR-4474 and miR-4717 are involved in the progression of F. nucleatum-induced CRC by posttranscriptionally regulating the target gene CREBBP. Public Library of Science 2019-04-05 /pmc/articles/PMC6450631/ /pubmed/30951563 http://dx.doi.org/10.1371/journal.pone.0215088 Text en © 2019 Feng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Feng, Yu-yang
Zeng, Dong-zhu
Tong, Ya-nan
Lu, Xiao-xue
Dun, Guo-dong
Tang, Bin
Zhang, Zhu-jun
Ye, Xin-li
Li, Qian
Xie, Jian-ping
Mao, Xu-hu
Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title_full Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title_fullStr Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title_full_unstemmed Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title_short Alteration of microRNA-4474/4717 expression and CREB-binding protein in human colorectal cancer tissues infected with Fusobacterium nucleatum
title_sort alteration of microrna-4474/4717 expression and creb-binding protein in human colorectal cancer tissues infected with fusobacterium nucleatum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450631/
https://www.ncbi.nlm.nih.gov/pubmed/30951563
http://dx.doi.org/10.1371/journal.pone.0215088
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