University of Oulu

Rusanen P, Marttila E, Uittamo J, HagstroÈm J, Salo T, Rautemaa-Richardson R (2017) TLR1-10, NF-κB and p53 expression is increased in oral lichenoid disease. PLoS ONE 12 (7): e0181361. https://doi.org/10.1371/journal.pone.0181361

TLR1-10, NF-κB and p53 expression is increased in oral lichenoid disease

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Author: Rusanen, Peter1; Marttila, Emilia2; Uittamo, Johanna2,3;
Organizations: 1Department of Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
2Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
3Research Unit on Acetaldehyde and Cancer, University of Helsinki, Helsinki, Finland
4Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland
5Cancer and Translational Medicine Research Unit, University of Oulu, and Medical Research Centre Oulu University Hospital, Oulu, Finland
6Division of Infection, Immunity and Respiratory Medicine, Faculty of Biology, Medicine and Health, University of Manchester; and University Hospital of South Manchester, Manchester, United Kingdom
Format: article
Version: published version
Access: open
Online Access: PDF Full Text (PDF, 18.4 MB)
Persistent link: http://urn.fi/urn:nbn:fi-fe2017112955162
Language: English
Published: Public Library of Science, 2017
Publish Date: 2017-11-29
Description:

Abstract

Toll-like receptors (TLRs) and nuclear factor-κB (NF-κB) in keratinocytes play an important role in dermatological autoimmune diseases. Tumour suppressor protein p53 regulates TLR expression. The aim of this study was to compare the expression of TLR1-TLR10, p53 and NF-κB in patients with oral lichenoid disease (OLD) with healthy mucosa. Oral mucosal biopsies from 24 patients with OLD and 26 healthy controls (HC) were analysed for the expression of TLR1-TLR10, NF-κB and p53 by immunohistochemistry. The expression of all TLRs was increased in OLD epithelia compared to HC samples and the difference was significant in TLR1, TLR3, TLR4, TLR5, TLR6 and TLR7. In the basement membrane zone, the immunoreactivity of TLR5 was significantly more intense in OLD compared to HC. In the intermediate layer, the immunoreactivity of NF-κB was significantly stronger in OLD, whereas the staining for p53 was more intense in all layers of OLD compared to HC samples. In OLD, a positive correlation between TLR2 and NF-κB in the basal layer and between TLR5, p53 and NF-κB in the intermediate layers was discovered. The expression of TLRs, p53 and NF-κB is increased in OLD, which may play a role in the pathogenesis of this chronic immune-mediated mucosal disease.

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Series: PLoS one
ISSN: 1932-6203
ISSN-E: 1932-6203
ISSN-L: 1932-6203
Volume: 12
Issue: 7
Article number: e0181361
DOI: 10.1371/journal.pone.0181361
OADOI: https://oadoi.org/10.1371/journal.pone.0181361
Type of Publication: A1 Journal article – refereed
Field of Science: 3122 Cancers
Subjects:
Funding: This work was supported by the Finnish Dental Society Apollonia and the Helsinki University Central Hospital (HUCH) Research.
Copyright information: © 2017 Rusanen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
  https://creativecommons.org/licenses/by/4.0/