Building a better understanding of the intracellular tyrosine kinase FrTK6-BRK by BRK

被引:83
作者
Brauer, Patrick M. [1 ]
Tyner, Angela L. [1 ]
机构
[1] Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2010年 / 1806卷 / 01期
基金
美国国家卫生研究院;
关键词
PTK6; BRK; Sik; Tyrosine kinase; Epithelia; Breast cancer; Colon cancer; BREAST-TUMOR KINASE; MAMMARY EPITHELIAL-CELLS; LONG-TERM SURVIVAL; GENE-EXPRESSION; IN-VITRO; THERAPEUTIC TARGET; SH2-KINASE LINKER; DISTINCT FAMILY; CANCER CELLS; SH3; DOMAIN;
D O I
10.1016/j.bbcan.2010.02.003
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
Protein tyrosine kinase 6 (PTK6), also referred to as breast tumor kinase BRK, is a member of a distinct family of kinases that is evolutionarily related to the SRC family of tyrosine kinases. While not expressed in the normal mammary gland, PTK6 expression is detected in a large proportion of human mammary gland tumors. In breast tumor cells, PTK6 promotes growth factor signaling and cell migration. PTK6 expression is also increased in a number of other epithelial tumors, including ovarian and colon cancer. In contrast, FTK6 is expressed in diverse normal epithelia, including the linings of the gastrointestinal tract, skin and prostate, where its expression correlates with cell cycle exit and differentiation. Disruption of the mouse Ptk6 gene leads to increased growth and impaired differentiation in the small intestine that is accompanied by increased AKT and Wnt signaling. Following total body irradiation, PTK6 expression is induced in proliferating progenitor cells of the intestine, where it plays an essential role in DNA-damage induced apoptosis. A distinguishing feature of FTK6 is its flexibility in intracellular localization, due to a lack of amino-terminal myristoylation/palmitoylation. Recently a number of substrates of PTK6 have been identified, including nuclear RNA-binding proteins and transcription factors. We discuss PTK6 signaling, its apparent conflicting roles in cancer and normal epithelia, and its potential as a therapeutic target in epithelial cancers. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 110 条
[11]   Osteopontin promotes vascular endothelial growth factor-dependent breast tumor growth and angiogenesis via autocrine and paracrine mechanisms [J].
Chakraborty, Goutam ;
Jain, Shalini ;
Kundu, Gopal C. .
CANCER RESEARCH, 2008, 68 (01) :152-161
[12]   ADAM-15: a metalloprotease that mediates inflammation [J].
Charrier-Hisamuddin, Laetitia ;
Laboisse, Christian L. ;
Merlin, Didier .
FASEB JOURNAL, 2008, 22 (03) :641-653
[13]   Brk activates Rac1 and promotes cell migration and invasion by phosphorylating paxillin [J].
Chen, HY ;
Shen, CH ;
Tsai, YT ;
Lin, FC ;
Huang, YP ;
Chen, RH .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (24) :10558-10572
[14]   A role for the GSG domain in localizing Sam68 to novel nuclear structures in cancer cell lines [J].
Chen, TP ;
Boisvert, FM ;
Bazett-Jones, DP ;
Richard, S .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (09) :3015-3033
[15]   Baseline gene expression predicts sensitivity to gefitinib in non-small cell lung cancer cell lines [J].
Coldren, Christopher D. ;
Helfrich, Barbara A. ;
Witta, Samir E. ;
Sugita, Michio ;
Lapadat, Razvan ;
Zeng, Chan ;
Baron, Anna ;
Franklin, Wilbur A. ;
Hirsch, Fred R. ;
Geraci, Mark W. ;
Bunn, Paul A., Jr. .
MOLECULAR CANCER RESEARCH, 2006, 4 (08) :521-528
[16]   Sam68 enhances the cytoplasmic utilization of intron-containing RNA and is functionally regulated by the nuclear kinase Sik/BRK [J].
Coyle, JH ;
Guzik, BW ;
Bor, YC ;
Jin, L ;
Eisner-Smerage, L ;
Taylor, SJ ;
Rekosh, D ;
Hammarskjöld, ML .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :92-103
[17]   Gene expansion and retention leads to a diverse tyrosine kinase superfamily in amphioxus [J].
D'Aniello, Salvatore ;
Irimia, Manuel ;
Maeso, Ignacio ;
Pascual-Anaya, Juan ;
Jimenez-Delgado, Senda ;
Bertrand, Stephanie ;
Garcia-Fernandez, Jordi .
MOLECULAR BIOLOGY AND EVOLUTION, 2008, 25 (09) :1841-1854
[18]   Sik (BRK) phosphorylates Sam68 in the nucleus and negatively regulates its RNA binding ability [J].
Derry, JJ ;
Richard, S ;
Carvajal, HV ;
Ye, X ;
Vasioukhin, V ;
Cochrane, AW ;
Chen, TP ;
Tyner, AL .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) :6114-6126
[19]   Altered localization and activity of the intracellular tyrosine kinase BRK/Sik in prostate tumor cells [J].
Derry, JJ ;
Prins, GS ;
Ray, V ;
Tyner, AL .
ONCOGENE, 2003, 22 (27) :4212-4220
[20]   PHOSPHORYLATION OF GAP AND GAP-ASSOCIATED PROTEINS BY TRANSFORMING AND MITOGENIC TYROSINE KINASES [J].
ELLIS, C ;
MORAN, M ;
MCCORMICK, F ;
PAWSON, T .
NATURE, 1990, 343 (6256) :377-381