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A20 as a Potential New Tool in Predicting Recurrence and Patient's Survival in Oral Squamous Cell Carcinoma.
| Content Provider | Europe PMC |
|---|---|
| Author | Spoerl, Steffen Erber, Ramona Gerken, Michael Taxis, Juergen Ludwig, Nils Nieberle, Felix Biermann, Niklas Geppert, Carol Immanuel Ettl, Tobias Hartmann, Arndt Beckhove, Philipp Reichert, Torsten E. Spanier, Gerrit Spoerl, Silvia |
| Editor | Wong, David |
| Copyright Year | 2023 |
| Abstract | Simple SummaryHere, we examined the presence and clinical relevance of A20 in oral squamous cell carcinoma (OSCC). Using a tissue microarray (TMA), immunohistochemical A20 expression as well as tumor-infiltrating lymphocytes (TIL) were analyzed. Hereby, A20 expression was significantly increased in TILs and patients with elevated A20 expression in stromal CD3+ cells showed ameliorated survival in uni- as well as multivariable analyses.AbstractA20, known as a potent inhibitor of NF-κB signaling, has been characterized in numerous clinical as well as preclinical studies. Recently, especially in various malignant diseases, the prognostic and therapeutic relevance of A20 was investigated. In oral squamous cell carcinoma (OSCC) however, the characterization of A20 is uncharted territory. We analyzed a tissue microarray (TMA) of 229 surgically-treated OSCC patients (2003–2013). Immunohistochemical (IHC) stainings were performed for A20 and CD3; additionally, standard haematoxylin-eosin staining was applied. IHC findings were correlated with a comprehensive dataset, comprising clinical and pathohistological information. A20 expression was analyzed in tumor cells as well as in tumor infiltrating lymphocytes (TILs) and correlated with the overall survival (OS) and recurrence-free survival (RFS) using uni- and multivariable Cox regression. The median follow-up time was 10.9 years and the A20 expression was significantly decreased in CD3+ TILs compared to mucosa-infiltrating lymphocytes (MILs). In the Kaplan–Meier analyses, higher A20 expression in TILs was correlated with better OS (p = 0.017) and RFS (p = 0.020). In the multivariable survival analysis, A20 overexpression correlated with improved OS (HR: 0.582; 95% CI 0.388–0.873, p = 0.009) and RFS (HR 0.605; 95% CI 0.411–0.889, p = 0.011). Our results indicate a novel prognostic role for A20 in OSCC. Due to its elevated expression in TILs, further research is highly desirable, which therefore could offer new therapeutic opportunities for patients suffering from OSCC. |
| Journal | Cancers |
| Volume Number | 15 |
| PubMed Central reference number | PMC9913673 |
| Issue Number | 3 |
| PubMed reference number | 36765630 |
| e-ISSN | 20726694 |
| DOI | 10.3390/cancers15030675 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2023-01-21 |
| Access Restriction | Open |
| Rights License | Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). © 2023 by the authors. |
| Subject Keyword | oral squamous cell carcinoma OSCC A20 tissue microarray TNFAIP3 |
| Content Type | Text |
| Resource Type | Article |
| Subject | Oncology Cancer Research |