Co-expression of epidermal growth factor receptor and transforming growth factor-α is independent of ras mutations in lung adenocarcinoma

被引:52
作者
Hsieh, ETK
Shepherd, FA
Tsao, MS
机构
[1] Princess Margaret Hosp, Univ Hlth Network, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[2] Princess Margaret Hosp, Univ Hlth Network, Div Hematol & Med Oncol, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Toronto, ON M5G 2M9, Canada
关键词
autocrine growth factor; tyrosine kinase receptor; signal transduction; immunohistochemistry;
D O I
10.1016/S0169-5002(00)00116-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The interaction of epidermal growth factor receptor (EGFR) and its ligand transforming growth factor-alpha (TGF-alpha) leads to an autocrine activation of the ras signaling pathway and putatively its oncogenic activity. II is thus hypothesized that the co-overexpression of EGFR-TGF alpha will be redundant hence rare in tumors with oncogenic ras mutations. To test this hypothesis, we studied by immunohistochemistry the expression of EGFR and TGF-cr. in primary non small cell lung cancers. Such putative EGFR autocrine loop activation was found in 73% of squamous cell carcinomas that rarely develop ras mutations. In contrast, EGFR-TGF alpha co-expression occurred with equal frequency in adenocarcinomas irrespective of their ras genotype. The results indicate that EGFR autocrine loop activity in adenocarcinoma may have alternative signaling activities aside from the activation of ias-MAP kinase pathway. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:151 / 157
页数:7
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