scholarly journals Immunohistochemical Analysis of Foxp3+, CD4+, CD8+ Cell Infiltrates and PD-L1 in Oral Squamous Cell Carcinoma

2017 ◽  
Vol 24 (3) ◽  
pp. 497-505 ◽  
Author(s):  
Olga Stasikowska-Kanicka ◽  
Małgorzata Wągrowska-Danilewicz ◽  
Marian Danilewicz
2020 ◽  
Vol 21 (11) ◽  
pp. 3317-3323
Author(s):  
Purnima Vadla ◽  
Sivaranjani Yeluri ◽  
G Deepthi ◽  
Venkateswara Rao Guttikonda ◽  
Sravya Taneeru ◽  
...  

Author(s):  
Ida Barca ◽  
Chiara Mignogna ◽  
Daniela Novembre ◽  
Francesco Ferragina ◽  
Maria Giulia Cristofaro

Background: Autophagy is a cellular process responsible for maintaining homeostasis; a dysregulation of this process is involved in the development and progression of neoplasms. Beclin-1 is one of the major proteins linked to autophagy. However, the data regarding the association between the role of Beclin-1 and the progression of Oral Squamous Cell Carcinoma (OSCC) are rather low. For this reason, the objective of this study is to evaluate, through immunohistochemical techniques, the prognostic role of the expression of Beclin-1 autophagy marker in patients with OSCC. Methods: This is a single-centre retrospective study that includes patients with OSCC admitted to the Maxillofacial Unit of “Magna Graecia” University between January 2019 and September 2020. All the samples obtained from surgery were treated with anti Beclin-1 antibodies and subjected to immunohistochemical methods. Results: A total of 26 samples were analysed and the following variables were evaluated for each: percentage of positive Beclin-1 expression by tumour cells, signal strength of tumour cells, and total score. The variables considered were first normalised according to the D’Agostino and Pearson test, then analysed using the Pearson linear correlation coefficient: a statistically significant correlation was found between the parameters infiltration-intensity (p = 0.0088), infiltration-percent (p = 0.0123), intensity-total score (p = 0.0060). Conclusions: The immunohistochemical evaluation of Beclin-1 revealed a statistically significant correlation between the intensity of the molecule’s expression and a greater degree of infiltration of the neoplasm. Beclin-1 can, therefore, be considered a valid prognostic index of disease.


2013 ◽  
Vol 4 ◽  
pp. 276-280 ◽  
Author(s):  
Łukasz Pyziak ◽  
Olga Stasikowska-Kanicka ◽  
Marian Danilewicz ◽  
Małgorzata Wągrowska-Danilewicz

2013 ◽  
Vol 42 (9) ◽  
pp. 676-681 ◽  
Author(s):  
Alexander Gröbe ◽  
Henning Hanken ◽  
Lan Kluwe ◽  
Maximilian Schöllchen ◽  
Silke Tribius ◽  
...  

Cancers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 494
Author(s):  
Junki Sakata ◽  
Akiyuki Hirosue ◽  
Ryoji Yoshida ◽  
Yuichiro Matsuoka ◽  
Kenta Kawahara ◽  
...  

Insulin-like growth factor (IGF) binding protein-3 (IGFBP-3) modulates various cell functions through IGF-dependent or independent mechanisms. However, its biological roles in the radiosensitivity of oral squamous cell carcinoma (OSCC) remain largely unknown. The purpose of this study was to determine the clinical significance and molecular mechanisms of the association between IGFBP-3 and OSCC radiosensitivity. We performed an immunohistochemical analysis of IGFBP-3 in 52 OSCC specimens from patients treated with preoperative chemoradiotherapy and surgery (phase II study). Associations between IGFBP-3 expression and clinicopathological features were also evaluated. In addition, we examined the effects of IGFBP-3 on post-X-ray irradiation radiosensitivity and DNA damage in vitro. High IGFBP-3 expression was significantly correlated with poor chemoradiotherapy responses and prognosis. With IGFBP-3 knockdown, irradiated OSCC cells exhibited significantly higher radiosensitivity compared with that of control cells. Moreover, IGFBP-3 depletion in OSCC cells reduced phosphorylation of the DNA-dependent protein kinase catalytic subunit (DNA-PKcs), which is required for DNA double-strand break repair during non-homologous end joining. These findings indicate that IGFBP-3 may have a significant role in regulating DNA repair and is be a potential biomarker for predicting clinical response to radiotherapy and prognosis in OSCC.


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