Germline


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
30 Apr 2024
Historique:
medline: 30 4 2024
pubmed: 30 4 2024
entrez: 30 4 2024
Statut: epublish

Résumé

Enhancers are critical for regulating tissue-specific gene expression, and genetic variants within enhancer regions have been suggested to contribute to various cancer-related processes, including therapeutic resistance. However, the precise mechanisms remain elusive. Using a well-defined drug-gene pair, we identified an enhancer region for dihydropyrimidine dehydrogenase (DPD,

Identifiants

pubmed: 38686795
doi: 10.7554/eLife.94075
pii: 94075
doi:
pii:

Substances chimiques

Fluorouracil U3P01618RT
Dihydrouracil Dehydrogenase (NADP) EC 1.3.1.2
Antineoplastic Agents 0
Antimetabolites, Antineoplastic 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : R01CA251065
Pays : United States

Informations de copyright

© 2024, Zhang et al.

Déclaration de conflit d'intérêts

TZ, AA, HH, KB, AE, RS, BB, ZT, ZW, DS, RD, CL No competing interests declared, FI Currently an AbbVie employee and receives stocks from the company, SO Reports current research support from Processa Pharmaceuticals, Inc, which are outside of the conduct of this study. Has previously served as an independent consultant for Processa Pharmaceuticals, Inc, in matters not related to this study

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Auteurs

Ting Zhang (T)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Alisa Ambrodji (A)

Department of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.

Huixing Huang (H)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Kelly J Bouchonville (KJ)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Amy S Etheridge (AS)

Eshelman School of Pharmacy, Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina at Chapel Hill, Chapel Hill, United States.

Remington E Schmidt (RE)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Brianna M Bembenek (BM)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Zoey B Temesgen (ZB)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Zhiquan Wang (Z)

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, United States.

Federico Innocenti (F)

Eshelman School of Pharmacy, Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina at Chapel Hill, Chapel Hill, United States.

Deborah Stroka (D)

Department of Visceral Surgery and Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Robert B Diasio (RB)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.

Carlo R Largiadèr (CR)

Department of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Steven M Offer (SM)

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, United States.
Department of Pathology, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, United States.
Holden Comprehensive Cancer Center, University of Iowa Carver College of Medicine, University of Iowa, Iowa City, United States.

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Classifications MeSH