Updating "Dataset of transcriptomic changes that occur in human preadipocytes over a 3-day course of exposure to 3,3',4,4',5-Pentachlorobiphenyl (PCB126)" with additional data on exposure to 2,2',5,5'-tetrachlorobiphenyl (PCB52) or its 4-hydroxy metabolite (4-OH-PCB52).

Adipose Diabetes Metabolite Obesity PCB52 Polychlorinated Biphenyls Preadipocytes RNAseq

Journal

Data in brief
ISSN: 2352-3409
Titre abrégé: Data Brief
Pays: Netherlands
ID NLM: 101654995

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 09 06 2023
revised: 10 07 2023
accepted: 11 07 2023
medline: 31 7 2023
pubmed: 31 7 2023
entrez: 31 7 2023
Statut: epublish

Résumé

Polychlorinated biphenyls (PCBs) were used extensively in building materials, including those used in schools. PCBs accumulate in fat, and exposure to PCBs is associated with the development of cancer, neurodevelopmental disorders, cardiovascular disease, obesity, and diabetes. The non-dioxin-like PCB congener, PCB52 (2,2',5,5'-tetrachlorobiphenyl), is found at one of the highest levels of any congener in school air. PCB52 is oxidized in the liver to hydroxylated forms, mainly 4-OH-PCB52 (2,2',5,5'-tetrachlorobiphenyl-4-ol). In a previous study, we reported on RNAseq data generated from exposure of human preadipocytes to the dioxin-like PCB congener, PCB126. In this new dataset, we used identical techniques to examine alterations in gene transcript levels in human preadipocytes exposed to PCB52 or 4-OH-PCB52 over a time course. This updated set of data provides a comprehensive transcriptional profile of changes that occur in preadipocytes exposed to PCB52 or 4-OH-PCB52 over time and allows for comparison of these changes between the parent compound and its hydroxy metabolite. The datasets will allow others to explore how PCB52 and 4-OH-PCB52 impact biological pathways in preadipocytes. Further studies can be performed to determine how these changes might lead to disease.

Identifiants

pubmed: 37520642
doi: 10.1016/j.dib.2023.109415
pii: S2352-3409(23)00516-4
pmc: PMC10375549
doi:

Types de publication

Journal Article

Langues

eng

Pagination

109415

Subventions

Organisme : NCI NIH HHS
ID : P30 CA086862
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES005605
Pays : United States
Organisme : NIEHS NIH HHS
ID : P42 ES013661
Pays : United States

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Francoise A Gourronc (FA)

Department of Microbiology and Immunology, University of Iowa.

Michael S Chimenti (MS)

Iowa Institute of Human Genetics, Bioinformatics Division, University of Iowa.

Hans-Joachim Lehmler (HJ)

Department of Occupational and Environmental Health, University of Iowa.

James A Ankrum (JA)

Roy J. Carver Department of Biomedical Engineering, University of Iowa.
Fraternal Order of Eagles Diabetes Research Center, University of Iowa.

Aloysius J Klingelhutz (AJ)

Department of Microbiology and Immunology, University of Iowa.
Fraternal Order of Eagles Diabetes Research Center, University of Iowa.

Classifications MeSH