Dissection of an impact of VDR and RXRA on the genomic activity of 1,25(OH) 2 D 3 in A431 squamous cell carcinoma.

Autor: Olszewska AM; Department of Histology, Medical University of Gdansk, 1a Debinki, 80-211Gdansk, Poland., Nowak JI; Department of Histology, Medical University of Gdansk, 1a Debinki, 80-211Gdansk, Poland., Myszczynski K; Centre of Biostatistics and Bioinformatics Analysis Medical University of Gdansk, 1aDebinki, 80-211 Gdansk, Poland., Słominski A; Department of Dermatology, University of Alabama at Birmingham, AL 35292, USA; Birmingham Veteran Administration Medical Center, Birmingham, AL 35292, USA., Żmijewski MA; Department of Histology, Medical University of Gdansk, 1a Debinki, 80-211Gdansk, Poland. Electronic address: mzmijewski@gumed.edu.pl.
Jazyk: angličtina
Zdroj: Molecular and cellular endocrinology [Mol Cell Endocrinol] 2024 Mar 01; Vol. 582, pp. 112124. Date of Electronic Publication: 2023 Dec 19.
DOI: 10.1016/j.mce.2023.112124
Abstrakt: Background: Human skin is the natural source, place of metabolism, and target for vitamin D 3 . The classical active form of vitamin D 3 , 1,25(OH) 2 D 3 , expresses pluripotent properties and is intensively studied in cancer prevention and therapy. To define the specific role of vitamin D 3 receptor (VDR) and its co-receptor retinoid X receptor alpha (RXRA) in genomic regulation, VDR or RXRA genes were silenced in the squamous cell carcinoma cell line A431 and treated with 1,25(OH) 2 D 3 at long incubation time points 24 h/72 h. Extending the incubation time of A431 WT (wild-type) cells with 1,25(OH) 2 D 3 resulted in a two-fold increase in DEGs (differentially expressed genes) and a change in the amount of downregulated from 37% to 53%. VDR knockout led to a complete loss of 1,25(OH) 2 D 3 -induced genome-wide gene regulation at 24 h time point, but after 72 h, 20 DEGs were found, of which 75% were downregulated, and most of them belonged to the gene ontology group "immune response". This may indicate the existence of an alternative, secondary response to 1,25(OH) 2 D 3 . In contrast, treatment of A431 ΔRXRA cells with 1,25(OH) 2 D 3 for 24 h only partially affected DEGs, suggesting RXRA-independent regulation. Interestingly, overexpression of classic 1,25(OH) 2 D 3 targets, like CYP24A1 (family 24 of subfamily A of cytochrome P450 member 1) or CAMP (cathelicidin antimicrobial peptide) was found to be RXRA-independent. Also, immunofluorescence staining of A431 WT cells revealed partial VDR/RXRA colocalization after 24 h and 72 h 1,25(OH) 2 D 3 treatment. Comparison of transcriptome changes induced by 1,25(OH) 2 D 3 in normal keratinocytes vs. cancer cells showed high cell type specific expression pattern with only a few genes commonly regulated by 1,25(OH) 2 D 3 . Activation of the genomic pathway at least partially reversed the expression of cancer-related genes, forming a basis for anti-cancer activates of 1,25(OH) 2 D 3 . In summary, VDR or RXRA independent genomic activities of 1,25(OH) 2 D 3 suggest the involvement of alternative factors, opening new challenges in this field.
Competing Interests: Declaration of competing interest 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.
(Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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