Fascin over-expression is associated with aggressiveness of oral squamous cell carcinoma

被引:51
作者
Lee, Terence K.
Poon, Ronnie T. P.
Man, Kwan
Guan, Xin-Yuan
Ma, Stephanie
Liu, Xiao Bing
Myers, Jeffrey N.
Yuen, Anthony P. W.
机构
[1] Univ Hong Kong, Fac Med, Dept Surg, Hong Kong, Peoples R China
[2] Univ Hong Kong, Fac Med, Dept Clin Oncol, Hong Kong, Peoples R China
[3] Univ Texas, MD Anderson Canc Ctr, Dept Head & Neck Surg, Houston, TX 77030 USA
关键词
aggressiveness; E-cadherin; fascin; OSCC;
D O I
10.1016/j.canlet.2007.03.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral squamous cell carcinoma (OSCC) is associated with a high potential of tumor recurrence and metastasis, leading to poor prognosis. Cell motility is an important factor in the progression and metastasis of cancers. Recently, Fascin has been linked to tumor progression by induction of cell motility. However, the precise roles of Fascin in OSCC have not been elucidated clearly. The aim of this study was to analyze the roles of Fascin in OSCC progression using OSCC clinical samples. We demonstrated that Fascin over-expression was found in OSCC clinical samples and its expression was significantly associated with nodal metastasis (p = 0.027), tumor recurrence (p < 0.001) and poor patients' overall survival (p = 0.013). Consistently, Fascin proteins were detected in all OSCC cell lines with the expression level corresponding to the invasion ability. To specifically investigate the mechanism of Fascin in OSCC, we examined the E-cadherin expression in the same set of OSCC specimens. Fascin was negatively correlated with E-cadherin expression (p = 0.018, r = -0.513). In conclusion, our findings suggested that Fascin over-expression might enhance OSCC aggressiveness, possibly by interacting with E-cadherin expression. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:308 / 315
页数:8
相关论文
共 35 条
[1]  
AZNAVOORIAN S, 1993, CANCER-AM CANCER SOC, V71, P1368, DOI 10.1002/1097-0142(19930215)71:4<1368::AID-CNCR2820710432>3.0.CO
[2]  
2-L
[3]  
Birner P, 2000, CANCER RES, V60, P4693
[4]   High-throughput tissue microarray analysis used to evaluate biology and prognostic significance of the E-cadherin pathway in non-small-cell lung cancer [J].
Bremnes, RM ;
Veve, R ;
Gabrielson, E ;
Hirsch, FR ;
Baron, A ;
Bemis, L ;
Gemmill, RM ;
Drabkin, HA ;
Franklin, WA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (10) :2417-2428
[5]  
BRYAN J, 1986, METHOD ENZYMOL, V134, P13
[6]   SEPARATION AND INTERACTION OF MAJOR COMPONENTS OF SEA-URCHIN ACTIN GEL [J].
BRYAN, J ;
KANE, RE .
JOURNAL OF MOLECULAR BIOLOGY, 1978, 125 (02) :207-224
[7]   Expression of mesothelin, fascin, and prostate stem cell antigen in primary ovarian mucinous tumors and their utility in differentiating primary ovarian mucinous tumors from metastatic pancreatic mucinous carcinomas in the ovary [J].
Cao, DF ;
Ji, HX ;
Ronnett, BM .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2005, 24 (01) :67-72
[8]   Loss of E-cadherin expression resulting from promoter hypermethylation in oral tongue carcinoma and its prognostic significance [J].
Chang, HW ;
Chow, V ;
Lam, KY ;
Wei, WI ;
Yuen, APW .
CANCER, 2002, 94 (02) :386-392
[9]   CDNA CLONING AND EXPRESSION OF THE HUMAN HOMOLOG OF THE SEA-URCHIN FASCIN AND DROSOPHILA SINGED GENES WHICH ENCODES AN ACTIN-BUNDLING PROTEIN [J].
DUH, FM ;
LATIF, F ;
WENG, YK ;
GEIL, L ;
MODI, W ;
STACKHOUSE, T ;
MATSUMURA, F ;
DUAN, DR ;
LINEHAN, WM ;
LERMAN, MI ;
GNARRA, JR .
DNA AND CELL BIOLOGY, 1994, 13 (08) :821-827
[10]   Actin-binding protein fascin expression in skin neoplasia [J].
Goncharuk, VN ;
Ross, JS ;
Carlson, JA .
JOURNAL OF CUTANEOUS PATHOLOGY, 2002, 29 (07) :430-438