The role of protein tyrosine phosphatases in colorectal cancer

被引:26
作者
Hoekstra, Elmer [1 ]
Peppelenbosch, Maikel P. [1 ]
Fuhler, Gwenny M. [1 ]
机构
[1] Univ Med Ctr Rotterdam, Erasmus MC, Dept Gastroenterol & Hepatol, NL-3015 CE Rotterdam, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2012年 / 1826卷 / 01期
关键词
Protein tyrosine phosphatases; Colorectal cancer; Signaling pathways; Novel treatment targets; WEIGHT PHOSPHOTYROSINE PHOSPHATASE; FAS-MEDIATED APOPTOSIS; AMINO-ACID-SEQUENCE; SRC FAMILY KINASES; COLON-CANCER; MOLECULAR-CLONING; CELL-CYCLE; GERMLINE MUTATIONS; PTEN EXPRESSION; DOWN-REGULATION;
D O I
10.1016/j.bbcan.2012.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer is one of the most common oncogenic diseases in the Western world. Several cancer associated cellular pathways have been identified, in which protein phosphorylation and dephosphorylation, especially on tyrosine residues, are one of most abundant regulatory mechanisms. The balance between these processes is under tight control by protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs). Aberrant activity of oncogenic PTKs is present in a large portion of human cancers. Because of the counteracting role of PTPs on phosphorylation-based activation of signal pathways, it has long been thought that PTPs must act as tumor suppressors. This dogma is now being challenged, with recent evidence showing that dephosphorylation events induced by some PTPs may actually stimulate tumor formation. As such, PTPs might form a novel attractive target for anticancer therapy. In this review, we summarize the action of different PTPs, the consequences of their altered expression in colorectal cancer, and their potential as target for the treatment of this deadly disease. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 188
页数:10
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