Ezrin in primary cutaneous melanoma

被引:80
作者
Ilmonen, S
Vaheri, A
Asko-Seljavaara, S
Carpen, O
机构
[1] Helsinki Univ Hosp, Dept Plast Surg, Helsinki, Finland
[2] Univ Helsinki, Dept Virol, Helsinki, Finland
[3] Univ Helsinki, Pathol & Anat & Neurosci Program, Biomedicum, Helsinki, Finland
基金
芬兰科学院;
关键词
ezrin; ERM protein; immunohistochemistry; melanoma; metastasis; prognostic factor;
D O I
10.1038/modpathol.3800300
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Ezrin is a member of the ezrin-radixin-moesin family of proteins that link the actin-containing cytoskeleton to the plasma membrane. Ezrin is also connected to signaling molecules involved in the regulation of cell survival, proliferation and migration. Here, we examined the expression of ezrin in 95 primary cutaneous melanomas and correlated ezrin expression with conventional prognostic factors and biomarkers. From 12 patients metastatic tissue samples were also examined. In addition to ezrin staining, Mib-1 proliferation antigen, p53 and Bcl-2 were evaluated. Ezrin immunoreactivity was seen in most tumors; only 19 (20%) melanomas were negative. A total of 48 (51%) tumors had weak immunoreactivity and 28 (29%) strong immunoreactivity. The intensity of ezrin immunoreactivity was associated with tumor thickness (Breslow, P = 0.0008) and with tumor invasion level (Clark, P = 0.004), thicker tumors having stronger immunoreactivity. Also, there was a correlation between higher Mib-1 index in tumors and strong ezrin expression. All metastatic samples (n = 12) showed positive ezrin immunoreactivity. In univariate analysis of survival, patients (n = 76) with positive ezrin immunoreactivity had worse clinical disease behavior than those (n = 19) without ezrin immunoreactivity, but the difference was not significant (P = 0.19). In multivariate analysis of survival, the ezrin immunoreactivity was not a significant marker. The results indicate that ezrin is expressed in most primary melanomas of the skin and in all metastatic tumors. Ezrin expression correlates with tumor thickness and level of invasion suggesting an association between ezrin expression and tumor progression.
引用
收藏
页码:503 / 510
页数:8
相关论文
共 55 条
[1]   The p53 network [J].
Agarwal, ML ;
Taylor, WR ;
Chernov, MV ;
Chernova, OB ;
Stark, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :1-4
[2]   High levels of ezrin expressed by human pancreatic adenocarcinoma cell lines with high metastatic potential [J].
Akisawa, N ;
Nishimori, I ;
Iwamura, T ;
Onishi, S ;
Hollingsworth, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 258 (02) :395-400
[3]  
[Anonymous], 2003, Cutaneous melanoma
[4]   An evidence-based staging system for cutaneous melanoma [J].
Balch, CM ;
Soong, SJ ;
Atkins, MB ;
Buzaid, AC ;
Cascinelli, N ;
Coit, DG ;
Fleming, ID ;
Gershenwald, JE ;
Houghton, A ;
Kirkwood, JM ;
McMasters, KM ;
Mihm, MF ;
Morton, DL ;
Reintgen, DS ;
Ross, MI ;
Sober, A ;
Thompson, JA ;
Thompson, JF .
CA-A CANCER JOURNAL FOR CLINICIANS, 2004, 54 (03) :131-149
[5]  
Bohling T, 1996, AM J PATHOL, V148, P367
[6]   MIB-1 immunoreactivity correlates with metastatic dissemination in primary thick cutaneous melanoma [J].
Boni, R ;
Doguoglu, A ;
Burg, G ;
Muller, B ;
Dummer, R .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 35 (03) :416-418
[8]   Regulation of cortical structure by the ezrin-radixin-moesin protein family [J].
Bretscher, A .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (01) :109-116
[9]   ERM proteins and merlin: Integrators at the cell cortex [J].
Bretscher, A ;
Edwards, K ;
Fehon, RG .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) :586-599
[10]  
Bretscher A, 1997, J CELL SCI, V110, P3011