[HTML][HTML] FSCN1 is an effective marker of poor prognosis and a potential therapeutic target in human tongue squamous cell carcinoma

Y Chen, T Tian, ZY Li, CY Wang, R Deng… - Cell Death & …, 2019 - nature.com
Y Chen, T Tian, ZY Li, CY Wang, R Deng, WY Deng, A Yang, YF Chen, H Li
Cell Death & Disease, 2019nature.com
To estimate the value of FSCN1 in evaluating the prognosis and guiding the targeted
therapy for patients with tongue squamous cell carcinoma (TSCC). Using the Oncomine
database, we found some genes especially FSCN1 differentially expressed between TSCC
samples and tongue normal samples. So we compared FSCN1 expression between TSCC
and normal cell lines and knocked down FSCN1 in TSCC cells to observe its influence on
the viability and trans-migration in vitro and tumor growth in vivo. Then we measured FSCN1 …
Abstract
To estimate the value of FSCN1 in evaluating the prognosis and guiding the targeted therapy for patients with tongue squamous cell carcinoma (TSCC). Using the Oncomine database, we found some genes especially FSCN1 differentially expressed between TSCC samples and tongue normal samples. So we compared FSCN1 expression between TSCC and normal cell lines and knocked down FSCN1 in TSCC cells to observe its influence on the viability and trans-migration in vitro and tumor growth in vivo. Then we measured FSCN1 expression in human cancer tissues and adjacent non-carcinoma tissues (ANT) and explored the relationship between FSCN1 expression and clinical pathological factors and prognosis in TSCC patients. We found that FSCN1 is expressed higher in TSCC cells than in normal cells. Knockdown of FSCN1 reduced TSCC cell viability and trans-migration in vitro and impaired tumor growth in vivo. FSCN1 also expressed higher in human TSCC than in ANT. In addition, FSCN1 expression was related to N classification, clinical stage and relapse. TSCC patients with over-expression of FSCN1 had worse prognosis. In conclusion, over-expression of FSCN1 indicates worse prognosis for patients with TSCC and FSCN1 may be a potential prognostic biomarker and therapeutic target in TSCC.
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