Expression of the cytoskeleton linker protein ezrin in human cancers

被引:151
作者
Bruce, Benjamin
Khanna, Gaurav
Ren, Ling
Landberg, Goran
Jirstrom, Karin
Powell, Charles
Borczuk, Alain
Keller, Evan T.
Wojno, Kirk J.
Meltzer, Paul
Baird, Kristin
McClatchey, Andrea
Bretscher, Anthony
Hewitt, Stephen M.
Khanna, Chand [1 ]
机构
[1] NCI, Ctr Canc Res, Tumor & Metastasis Biol Sect, Bethesda, MD 20892 USA
[2] Howard Hughes Med Inst, Bethesda, MD USA
[3] Lund Univ, Malmo Univ Hosp, S-20502 Malmo, Sweden
[4] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[5] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[6] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
[7] NHGRI, Canc Genet Branch, Bethesda, MD USA
[8] Harvard Univ, Massachusetts Gen Hosp, Ctr Canc, Dept Pathol, Charlestown, MA USA
[9] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY USA
[10] Natl Canc Inst, Ctr Canc Res, Pathol Lab, Tissue Army Res Program, Bethesda, MD USA
关键词
ezrin; merlin; immunohistochemistry; tissue microarray; biomarker; prognosis;
D O I
10.1007/s10585-006-9050-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Expression of the metastasis-associated protein, ezrin, in over 5,000 human cancers and normal tissues was analyzed using tissue microarray immunohistochemistry. Ezrin staining was compared between cancers and their corresponding normal tissues, between cancers of epithelial and mesenchymal origin, in the context of the putative inhibitor protein, merlin, and against clinicopathological data available for breast, lung, prostate cancers and sarcomas. Ezrin was found in most cancers and normal tissues at varying levels of intensity. In general ezrin was expressed at higher levels in sarcomas than in carcinomas. By normalizing the expression of ezrin in each cancer using ezrin expression found in the corresponding normal tissue, significant associations between ezrin were found in advancing histological grade in sarcomas (P = 0.02) and poor outcome in breast cancer (P = 0.025). Clinicopathologic associations were not changed by simultaneous assessment of ezrin and merlin in each patient sample for the cancer types examined. These data support a role for ezrin in the biology of human cancers and the need for additional studies in breast cancer and sarcoma patients that may validate ezrin as a marker of cancer progression and as a potential target for cancer therapy.
引用
收藏
页码:69 / 78
页数:10
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