Expression of the nerve growth factor receptors TrkA and p75 in malignant mesothelioma

被引:32
作者
Davidson, B
Reich, R
Lazarovici, P
Florenes, VA
Risberg, B
Nielsen, S
Sert, B
Bedrossian, C
机构
[1] Univ Oslo, Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[2] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Dept Pharmacol & Expt Therapeut, IL-91120 Jerusalem, Israel
[3] Aalborg Hosp, Dept Pathol, DK-9000 Aalborg, Denmark
[4] Univ Oslo, Norwegian Radium Hosp, Dept Gynecol Oncol, N-0310 Oslo, Norway
[5] Northwestern Univ, Dept Pathol, Chicago, IL 60611 USA
[6] Hebrew Univ Jerusalem, David R Bloom Ctr Pharm, IL-91905 Jerusalem, Israel
关键词
malignant mesothelioma; neurotrophins; tyrosine kinase receptors; p75; effusions;
D O I
10.1016/j.lungcan.2003.11.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of the present report was to study the expression of the tow affinity nerve growth factor (NGF) receptor p75 and of the activated high-affinity NGF receptor TrkA in malignant mesothelioma (MM). In addition, to analyze whether expression of these receptors is site-related (pleural. versus peritoneal MM, solid lesions versus effusions). Sections from 81 MM (57 biopsies, 24 effusions) were analyzed. Sixty-one mesotheliomas were of pleural origin, while the remaining 20 were peritoneal Effusion specimens consisted of 6 peritoneal and 18 pleural. effusions, while biopsies consisted of 14 peritonea[ and 43 pleura[ lesions. Specimens were immunohistochemically stained using antibodies against p75 and phospho-TrkA (p-TrkA). Six effusions were additionally analyzed for p-TrkA expression using immunoblotting (113). p-TrkA membrane expression (66/81 specimens; 81%) was by far more frequent than that of p75 (26/81 specimens; 32%). In addition, p-TrkA expression was significantly higher in peritoneal. MM compared to their pleural counterparts (20/20 versus 46/61 positive tumors; P = 0.014). p-TrkA membrane expression was marginally higher in effusions (P = 0.058), while the opposite was true for p75 membrane expression (P = 0.008) and p-TrkA cytoplasmic expression (P = 0.003). In conclusion, our results document for the first time frequent expression of p-TrkA and tower expression of p75 in MM, in agreement with the biological aggressiveness of this tumor. The enhanced expression of p-TrkA in peritoneal. MM, tumors that appear in younger patients, and in effusions as compared to solid tumors, suggest that p-TrkA plays a significant role in the biology of this disease and may aid in defining tumor progression in this setting. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:159 / 165
页数:7
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