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PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness

BACKGROUND: Our previous study revealed that PLAGL2 or POFUT1 can promote tumorigenesis and maintain significant positive correlations in colorectal cancer (CRC). However, the mechanism leading to the co-expression and the underlying functional and biological implications remain unclear. METHODS: Cl...

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Autores principales: Li, Daojiang, Lin, Changwei, Li, Nanpeng, Du, Yuheng, Yang, Chunxing, Bai, Yang, Feng, Zhicai, Su, Chen, Wu, Runliu, Song, Shenglei, Yan, Peicheng, Chen, Miao, Jain, Arad, Huang, Lihua, Zhang, Yi, Li, Xiaorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642334/
https://www.ncbi.nlm.nih.gov/pubmed/31279780
http://dx.doi.org/10.1016/j.ebiom.2019.06.051
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author Li, Daojiang
Lin, Changwei
Li, Nanpeng
Du, Yuheng
Yang, Chunxing
Bai, Yang
Feng, Zhicai
Su, Chen
Wu, Runliu
Song, Shenglei
Yan, Peicheng
Chen, Miao
Jain, Arad
Huang, Lihua
Zhang, Yi
Li, Xiaorong
author_facet Li, Daojiang
Lin, Changwei
Li, Nanpeng
Du, Yuheng
Yang, Chunxing
Bai, Yang
Feng, Zhicai
Su, Chen
Wu, Runliu
Song, Shenglei
Yan, Peicheng
Chen, Miao
Jain, Arad
Huang, Lihua
Zhang, Yi
Li, Xiaorong
author_sort Li, Daojiang
collection PubMed
description BACKGROUND: Our previous study revealed that PLAGL2 or POFUT1 can promote tumorigenesis and maintain significant positive correlations in colorectal cancer (CRC). However, the mechanism leading to the co-expression and the underlying functional and biological implications remain unclear. METHODS: Clinical tumor tissues and TCGA dataset were utilized to analyze the co-expression of PLAGL2 and POFUT1. Luciferase reporter assays, specially made bidirectional promoter vectors and ectopic expression of 3’UTR were employed to study the mechanisms of co-expression. In vitro and in vivo assays were performed to further confirm the oncogenic function of both. The sphere formation assay, immunofluorescence, Western blot and qRT-PCR were performed to investigate the effect of both genes in colorectal cancer stem cells (CSCs). FINDINGS: PLAGL2 and POFUT1 maintained co-expression in CRC (r = 0.91, p < .0001). An evolutionarily conserved bidirectional promoter, rather than post-transcriptional regulation by competing endogenous RNAs, caused the co-expression of PLAGL2 and POFUT1 in CRC. The bidirectional gene pair PLAGL2/POFUT1 was subverted in CRC and acted synergistically to promote colorectal tumorigenesis by maintaining stemness of colorectal cancer stem cells through the Wnt and Notch pathways. Finally, PLAGL2 and POFUT1 share transcription factor binding sites, and introducing mutations into promoter regions with shared transcription regulatory elements led to a decrease in the PLAGL2/POFUT1 promoter activity in both directions. INTERPRETATION: Our team identified for the first time a bidirectional promoter pair oncogene, PLAGL2-POFUT1, in CRC. The two genes synergistically promote the progression of CRC and affect the characteristics of CSCs, which can offer promising intervention targets for clinicians and researchers. FUND: National Nature Science Foundation of China, the Hunan province projects of Postgraduate Independent Exploration and Innovation of Central South University.
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spelling pubmed-66423342019-07-23 PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness Li, Daojiang Lin, Changwei Li, Nanpeng Du, Yuheng Yang, Chunxing Bai, Yang Feng, Zhicai Su, Chen Wu, Runliu Song, Shenglei Yan, Peicheng Chen, Miao Jain, Arad Huang, Lihua Zhang, Yi Li, Xiaorong EBioMedicine Research paper BACKGROUND: Our previous study revealed that PLAGL2 or POFUT1 can promote tumorigenesis and maintain significant positive correlations in colorectal cancer (CRC). However, the mechanism leading to the co-expression and the underlying functional and biological implications remain unclear. METHODS: Clinical tumor tissues and TCGA dataset were utilized to analyze the co-expression of PLAGL2 and POFUT1. Luciferase reporter assays, specially made bidirectional promoter vectors and ectopic expression of 3’UTR were employed to study the mechanisms of co-expression. In vitro and in vivo assays were performed to further confirm the oncogenic function of both. The sphere formation assay, immunofluorescence, Western blot and qRT-PCR were performed to investigate the effect of both genes in colorectal cancer stem cells (CSCs). FINDINGS: PLAGL2 and POFUT1 maintained co-expression in CRC (r = 0.91, p < .0001). An evolutionarily conserved bidirectional promoter, rather than post-transcriptional regulation by competing endogenous RNAs, caused the co-expression of PLAGL2 and POFUT1 in CRC. The bidirectional gene pair PLAGL2/POFUT1 was subverted in CRC and acted synergistically to promote colorectal tumorigenesis by maintaining stemness of colorectal cancer stem cells through the Wnt and Notch pathways. Finally, PLAGL2 and POFUT1 share transcription factor binding sites, and introducing mutations into promoter regions with shared transcription regulatory elements led to a decrease in the PLAGL2/POFUT1 promoter activity in both directions. INTERPRETATION: Our team identified for the first time a bidirectional promoter pair oncogene, PLAGL2-POFUT1, in CRC. The two genes synergistically promote the progression of CRC and affect the characteristics of CSCs, which can offer promising intervention targets for clinicians and researchers. FUND: National Nature Science Foundation of China, the Hunan province projects of Postgraduate Independent Exploration and Innovation of Central South University. Elsevier 2019-07-04 /pmc/articles/PMC6642334/ /pubmed/31279780 http://dx.doi.org/10.1016/j.ebiom.2019.06.051 Text en © 2019 The Authors 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 Research paper
Li, Daojiang
Lin, Changwei
Li, Nanpeng
Du, Yuheng
Yang, Chunxing
Bai, Yang
Feng, Zhicai
Su, Chen
Wu, Runliu
Song, Shenglei
Yan, Peicheng
Chen, Miao
Jain, Arad
Huang, Lihua
Zhang, Yi
Li, Xiaorong
PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title_full PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title_fullStr PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title_full_unstemmed PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title_short PLAGL2 and POFUT1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
title_sort plagl2 and pofut1 are regulated by an evolutionarily conserved bidirectional promoter and are collaboratively involved in colorectal cancer by maintaining stemness
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642334/
https://www.ncbi.nlm.nih.gov/pubmed/31279780
http://dx.doi.org/10.1016/j.ebiom.2019.06.051
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