Abstract
Despite many years of intensive investigation, real biological role of SERPINB2 is largely unknown. However, recent high throughput studies suggest its function in inflammation, influence on autoimmune disorders, and modulation of processes leading to carcinogenesis. SERPINB2 expression is acutely upregulated by many different stimuli, among others by aryl hydrocarbon receptor ligands. Mechanisms of regulation of SERPINB2 expression, involvement of the gene in processes leading to inflammation or carcinogenesis, and its interplay with aryl hydrocarbon receptor are subject of present review.
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Abbreviations
- P-TEFb:
-
positive transcription elongation factor
- CDK9:
-
cyclin-dependent kinase 9 associated with P-TEFb
- NELF:
-
negative elongation factor
- eRNA:
-
enhancer RNA
- TPA:
-
12-O-tetradecanoylphorbol-13-acetate
- AP-1:
-
activator protein 1
- CRE :
-
cAMP-responsive element
- BNF:
-
β-naphthoflavone
- BaP:
-
benzo[a]pyrene
- TCDD:
-
2,3,7,8-tetrachlorodibenzo-p-dioxin
- LPS:
-
bacterial lipopolysaccharide
- SERPINB2:
-
serpin peptidase inhibitor B2
- AhR:
-
aryl hydrocarbon receptor
- CYP1A1:
-
cytochrome P450 1A1
- PXK:
-
PX domain containing serine/threonine kinase
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This study was funded by statutory funding (Institute of Human Genetics, PAS).
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Communicated by: Michal Witt
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Brauze, D. SERPINB2—its regulation and interplay with aryl hydrocarbon receptor. J Appl Genetics 62, 99–105 (2021). https://doi.org/10.1007/s13353-020-00606-z
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DOI: https://doi.org/10.1007/s13353-020-00606-z