Journal of investigative and clinical dentistry, volume 10, issue 4
Immunohistochemical expression of tumor necrosis factor‐like weak inducer of apoptosis and fibroblast growth factor‐inducible immediate early response protein 14 in oral squamous cell carcinoma and its implications
Swetha Acharya
1
,
Prashant Prabhu
1
,
Vidya S Patil
2
,
Anirudh B. Acharya
3
,
Krithi Nikhil
4
1
Department of Oral Pathology and Microbiology SDM College of Dental Sciences and Hospital Dharwad India
|
2
Department of Biochemistry SDM College of Medical Sciences and HospitalDharwad India
|
3
Department of Periodontics SDM College of Dental Sciences and Hospital Dharwad India
|
4
BiostatisticianDepartment of Public Health Dentistry, SDM College of Dental Sciences & Hospital Dharwad India
|
Publication type: Journal Article
Publication date: 2019-09-21
SJR: —
CiteScore: —
Impact factor: —
ISSN: 20411618, 20411626
PubMed ID:
31541512
General Medicine
Abstract
To study the expression of tumor necrosis factor-like weak inducer of apoptosis (TWEAK) and fibroblast growth factor-inducible immediate early response protein 14 (Fn14) in oral squamous cell carcinoma (OSCC), to elucidate the possible role of TWEAK-Fn14 in OSCC development.Immunohistochemistry for TWEAK-Fn14 was performed on 61 oral mucosal samples: healthy oral mucosa (HOM; N = 15); oral dysplastic lesions (ODL; N = 15); and OSCC (N = 31). Extent of staining (ES) and immunoreactive score (IRS) were assessed. The data was statistically analyzed.All OSCC expressed TWEAK, and the Fn14 expression was noted in 90% of OSCC. A significant difference in the TWEAK and Fn14 expression was noted among the groups. ES and IRS of TWEAK-Fn14 significantly increased in OSCC compared with ODL and HOM. ES of TWEAK was significantly higher than Fn14 in all 3 groups. ES of TWEAK-Fn14 was significantly higher at the invasive tumor front (ITF) than in the whole tumor. TWEAK-Fn14 showed a significant association with clinicopathological parameters of prognostic significance.Findings suggest that TWEAK and Fn14 may participate in the growth and progression of OSCC. Increased expression of TWEAK-Fn14 at the ITF may facilitate increased proliferation, altered differentiation and invasion.
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