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KiSS‐1 expression in oral squamous cell carcinoma and its prognostic significance
Author(s) -
Shin WuiJung,
Cho YoungAh,
Kang KyungRim,
Kim JiHoon,
Hong SeongDoo,
Lee JaeIl,
Hong SamPyo,
Yoon HyeJung
Publication year - 2016
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/apm.12507
Subject(s) - kiss (tnc) , basal cell , medicine , expression (computer science) , oncology , cancer research , computer network , computer science , programming language
Downregulated expression of Ki SS ‐1 has been correlated with tumor progression, metastasis, and patient prognosis in various human malignancies. However, there is no information regarding the expression of Ki SS ‐1 in oral squamous cell carcinoma ( OSCC ). Our aims were to examine Ki SS ‐1 expression in OSCC tissue samples and cell lines and to determine its prognostic significance. Ki SS ‐1 expression was significantly lower in lymph node ( LN ) metastases than in primary tumor tissues. Five of six OSCC cell lines showed absence or relatively low expression of Ki SS ‐1. Correlations between Ki SS ‐1 expression and clinicopathological parameters were statistically assessed. There were significant correlations between Ki SS ‐1 expression and LN metastasis (p = 0.007), TNM stage (p = 0.024), and local recurrence (p = 0.012). In the Kaplan–Meier survival analysis, negative Ki SS ‐1 expression significantly correlated with poorer overall survival ( OS ) and disease‐free survival ( DFS ) (p = 0.000 and 0.000, respectively). Multivariate analysis using Cox regression modeling revealed that Ki SS ‐1 expression was an independent prognostic factor for both OS and DFS (p = 0.001 and 0.000, respectively). Our findings suggested that Ki SS ‐1 downregulation may play a role in tumor progression and metastasis of OSCC and may be a reliable biomarker for predicting clinical outcome in OSCC .
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