Identification of a Putative Enhancer RNA for EGFR in Hyper-Accessible Regions in Esophageal Squamous Cell Carcinoma Cells by Analysis of Chromatin Accessibility Landscapes.

AP-1 ATAC-seq digital droplet PCR enhancer RNA (eRNA) esophageal cancer non-coding RNA (ncRNA) transcription factor binding tyrosine kinase inhibitor (TKI)

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 14 06 2021
accepted: 20 09 2021
entrez: 1 11 2021
pubmed: 2 11 2021
medline: 2 11 2021
Statut: epublish

Résumé

Abnormal genetic and epigenetic modifications play a key role in esophageal cancer. By Assay for Transposase-Accessible Chromatin by sequencing (ATAC-seq), this study compared chromatin accessibility landscapes among two esophageal squamous cell carcinoma (ESCC) cell lines, KYSE-30 and KYSE-150, and a non-cancerous esophageal epithelial cell line, HET-1A. Data showed that hyper-accessible regions in ESCC cells contained genes related with cancer hallmarks, such as epidermal growth factor receptor (EGFR). Multi-omics analysis and digital-droplet PCR results demonstrated that several non-coding RNAs in EGFR upstream were upregulated in ESCC cells. Among them, one appeared to act as an enhancer RNA responsible for EGFR overexpression. Further motif analysis and pharmacological data suggested that AP-1 family transcription factors were able to bind the hyper-accessible regions and thus to regulate cancer cell proliferation and migration. This study discovered a putative enhancer RNA for EGFR gene and the reliance of ESCC on AP-1 transcription factor.

Identifiants

pubmed: 34722266
doi: 10.3389/fonc.2021.724687
pmc: PMC8554337
doi:

Types de publication

Journal Article

Langues

eng

Pagination

724687

Informations de copyright

Copyright © 2021 Choi, Sathe, Mathé, Xing and Pan.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Sangyong Choi (S)

College of Nursing and Health Innovation, University of Texas at Arlington, Arlington, TX, United States.
Department of Nutritional Sciences, College of Agriculture, Health and Natural Resources, University of Connecticut, Storrs, CT, United States.

Adwait Sathe (A)

Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Ewy Mathé (E)

Department of Biomedical Informatics, The Ohio State University Wexner Medical Center, Columbus, OH, United States.
Division of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Rockville, MD, United States.

Chao Xing (C)

Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Zui Pan (Z)

College of Nursing and Health Innovation, University of Texas at Arlington, Arlington, TX, United States.

Classifications MeSH