Pdcd4 inhibits growth of tumor cells by suppression of carbonic anhydrase type II

被引:67
作者
Lankat-Buttgereit, B
Gregel, C
Knolle, A
Hasilik, A
Arnold, R
Göke, R
机构
[1] Univ Marburg, Clin Res Unit Gastrointestinal Endocrinol, D-35033 Marburg, Germany
[2] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[3] Univ Marburg, Inst Physiol Chem, D-35033 Marburg, Germany
关键词
Pdcd4; carbonic anhydrase; endocrine tumor; ethoxyzolamide; translation;
D O I
10.1016/j.mce.2003.10.058
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To identify new genes that are upregulated during apoptosis we previously cloned rat pdcd4. While the role of pdcd4 is still unclear it seems to possess a tumor suppressor activity. Pdcd4 directly interacts with the RNA helicase eIF4A and inhibits protein synthesis by interfering with the assembly of the cap-dependent translation initiation complex. In the present Study, we show that pdcd4 Suppresses carbonic anhydrase type II protein expression in HEK293 and Bon-1 carcinoid cells. Since tumor cells require a high bicarbonate flux for their growth, carbonic anhydrase suppression results in growth inhibition. Similar to pdcd4, carbonic anhydrase inhibitor ethoxyzolamide reduces growth of several endocrine tumor cell lines. Thus, the translation inhibitor pdcd4 represses endocrine tumor cell growth by Suppression of carbonic anhydase II. Furthermore, carbonic anhydrase inhibitors might represent promising tools for anti-endocrine tumor treatment. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:149 / 153
页数:5
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