Focal adhesion kinase expression in human neuroblastoma: Immunohistochemical and real-time PCR analyses

被引：52

作者：

Beierle, Elizabeth A. ^{[2
]}

Massoll, Nicole A. ^{[1
]}

Hartwich, Joseph ^{[2
]}

Kurenova, Elena V. ^{[2
]}

Golubovskaya, Vita M. ^{[2
]}

Cance, William G. ^{[2
]}

McGrady, Patrick ^{[3
]}

London, Wendy B. ^{[3
]}

机构：

[1] Univ Florida, Dept Pathol, Gainesville, FL 32610 USA

[2] Univ Florida, Coll Med, Dept Surg, J Hillis Miller Hlth Sci Ctr, Gainesville, FL 32610 USA

[3] Childrens Oncol Grp, Epidemiol & Hlth Policy Res, Gainesville, FL USA

来源：

CLINICAL CANCER RESEARCH | 2008年 / 14卷 / 11期

关键词：

D O I：

10.1158/1078-0432.CCR-07-1511

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Purpose: The focal adhesion kinase (FAK) is a nonreceptor protein tyrosine kinase important in signaling between cells and their extracellular matrix. Studies have shown that FAK expression is up-regulated in several human tumors and is related to tumor progression. We recently found an increase in p125(FAK) expression in human neuroblastoma cells lines and wished to determine its expression in human neuroblastoma specimens and evaluate for a possible correlation between p125(FAK) expression and known prognostic factors for neuroblastoma. We hypothesized that p125(FAK) expression would be up-regulated in advanced human neuroblastomas. Experimental Design: Using immunohistochemical techniques with monoclonal antibody 4.47 specific for p125(FAK) expression, we analyzed 70 formalin-fixed, paraffin-embedded human neuroblastoma specimens for p125(FAK) staining. In addition, real-time PCR was used to determine the abundance of FAK mRNA in 17 matched human neuroblastoma mRNA specimens. Results: FAK staining was present in 51 of the 70 tumor specimens (73%). Immunohistochemical staining of p125(FAK) in the ganglion-type tumor cells correlated with advanced International Neuroblastoma Staging System tumor stages and FAK mRNA abundance. In addition, p125(FAK) staining was significantly increased in stage IV tumors with amplification of the N-MYC oncogene. Conclusions: These novel findings provide evidence that FAK is expressed by advanced-stage neuroblastoma and provide a rationale for targeting FAK in the treatment of this tumor.

引用

页码：3299 / 3305

页数：7