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HSP105 expression in oral squamous cell carcinoma: Correlation with clinicopathological features and outcomes
Author(s) -
Arvanitidou Souzana,
MartinelliKläy Carla P.,
Samson Jacky,
Lobrinus Johannes A.,
Dulguerov Nicolas,
Lombardi Tommaso
Publication year - 2020
Publication title -
journal of oral pathology and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.887
H-Index - 83
eISSN - 1600-0714
pISSN - 0904-2512
DOI - 10.1111/jop.13007
Subject(s) - immunohistochemistry , medicine , heat shock protein , malignancy , pathology , stage (stratigraphy) , staining , carcinoma , cancer , hsp70 , oncology , apoptosis , biology , paleontology , biochemistry , gene
Background Heat shock proteins (HSPs) are released in response to stress situations, such as heat, inflammation, and infection. They are also involved in the tumor cell proliferation and prevention of apoptosis. Heat shock protein 105 (Hsp105/110) is a high‐molecular‐weight protein, which has been reported in many cancer types but few studies have been carried out on oral squamous cell carcinoma (OSCC). In the current study, we have focused on HSP105 expression on OSCC and evaluated their correlation with tumor clinicopathological parameters and patients' survival. Methods A retrospective study included 70 patients with OSCC of which 50 patients (71.4%) were male and 20 (28.6%) were female. The patient's information, including age, location, TNM stage, histological grade, regional metastasis, recurrence, and survival, were collected. Immunohistochemical staining for HSP105 was performed. The healthy oral mucosa (n = 10) was used as a control. The staining intensity and percentage of stained cells were semi‐quantitatively evaluated, and HSP105 expression was correlated with tumor clinicopathological features and patient survival. Results Statistical analysis for HSP105 showed that there was no significant correlation with tumor clinicopathological features. However, HSP105 overexpression was associated with a decrease in the duration of patients' survival ( P  = .042). Conclusion This result suggests that the increased expression of the HSP105 in the OSCC could be a prognostic factor for malignancy.

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