Overexpression of sprouty2 in human oral squamous cell carcinogenesis. (March 2018)

• Record Type: Journal Article
• Authors: Liao, Pei-Hsien; Wang, Yen-Yun; Wang, Wen-Chen; Chen, Chung-Ho; Kao, Yu-Hsun; Hsu, Jing-Wei; Chen, Ching-Yi; Chen, Ping-Ho; Yuan, Shyng-Shiou; Chen, Yuk-Kwan
• Is Part Of: Archives of oral biology. Volume 87(2018)
• Page Start: 131
• Page End: 142
• Publication Date: 2018-03
• Subjects: Sprouty2 -- Oral carcinogenesis -- Oral squamous cell carcinoma -- Oral potentially malignant disorder -- Human; Mouth -- Periodicals; Mouth -- Diseases -- Periodicals; Dentistry -- Periodicals; Electronic journals; 617.6005
• DOI: 10.1016/j.archoralbio.2017.12.021
• Languages: English
• ISSNs: 0003-9969

Abstract

Highlights: SPRY2 is upregulated in human oral squamous cell carcinogenesis. SPRY2 protein was increased in OSCC patients with lymph-node metastasis and OPMD patients with malignant transformation. SPRY2 overexpression implies potential clinical relevance in human oral squamous cell carcinogenesis. Abstract: Objective: This study investigated SPRY2 expression in human oral potentially malignant disorders (OPMDs) and oral squamous cell carcinomas (OSCCs). Methods: 75 OSCCs, 23 OPMDs with malignant transformation (MT), 17 OPMDs without MT, and eight normal oral mucosa (NOM) tissues were used for immunohistochemical staining; three OSCC tissues with normal tissue counterparts were used for western blotting. Three human oral cancer cell lines (OCCLs), an oral precancer cell line (DOK), and a NOM primary culture (NOMPC) were used for western blotting; OCCLs and NOMPC were employed for real-time quantitative reverse transcription-polymerase chain reaction. OCCLs were evaluated in terms of proliferation, migration, invasion and BRAF V600E point mutation assays. Results: Significantly increased SPRY2 protein expression was observed in OSCCs as compared with NOM, and SPRY2 expression also differed between OSCC patients with and without lymph-node metastasis. SPRY2 protein and mRNA expressions were significantly enhanced as compared with NOMPC. Increased phospho-ERK expression was observed in OCCLs as compared with NOMPC. Significant decreases in the proliferation rate, degrees of migration and invasion were noted in OCCLs with SPRY2 siRNA transfection as compared with those without SPRY2 siRNA transfection. No BRAF V600E point mutation was observed for OCCLs as compared with NOMPC. A significantly increased SPRY2 protein level was noted in OPMDs with MT as compared to those without MT, and was also found in OPMDs with MT in comparison with NOM, as well as in DOK in comparison with NOMPC. Conclusions: Our results indicated that SPRY2 overexpression is associated with human oral squamous-cell carcinogenesis.