Fundamentals of transcription factors and their impact on pancreatic development and cancer

被引:4
作者
Fernandez-Zapico, ME [1 ]
Bramati, PS [1 ]
Zakaria, S [1 ]
Kaczynski, JA [1 ]
Urrutia, R [1 ]
机构
[1] Mayo Clin, Gastroenterol Res Unit, Rochester, MN USA
关键词
cancer; development; pancreas; transcription factors;
D O I
10.1159/000071765
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Transcription factors are proteins that regulate gene expression by modulating the synthesis of messenger RNA. Since this process, known as gene transcription, is often the dominant control point in the production of many proteins, transcription factors are key regulators of numerous cellular functions, including secretion, proliferation, differentiation, and apoptosis. Most transcription factors are also the final effectors of signaling pathways that transduce signals from the cell membrane to the nucleus. Therefore alterations in the activity or expression of some transcription factors have a significant impact on the biology of human cells and may lead to the development of diseases. In this article we review this field of research with a particular emphasis on the role of transcription factors in pancreatic development and cancer Copyright (C) 2003 S. Karger AG, Basel and IAP.
引用
收藏
页码:276 / 283
页数:8
相关论文
共 82 条
[1]   Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells [J].
Ahlgren, U ;
Pfaff, SL ;
Jessell, TM ;
Edlund, T ;
Edlund, H .
NATURE, 1997, 385 (6613) :257-260
[2]   β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes [J].
Ahlgren, U ;
Jonsson, J ;
Jonsson, L ;
Simu, K ;
Edlund, H .
GENES & DEVELOPMENT, 1998, 12 (12) :1763-1768
[3]   Notch signalling controls pancreatic cell differentiation [J].
Apelqvist, Å ;
Li, H ;
Sommer, L ;
Beatus, P ;
Anderson, DJ ;
Honjo, T ;
de Angelis, MH ;
Lendahl, U ;
Edlund, H .
NATURE, 1999, 400 (6747) :877-881
[4]   A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro [J].
Armstrong, JA ;
Bieker, JJ ;
Emerson, BM .
CELL, 1998, 95 (01) :93-104
[5]   Smads as transcriptional co-modulators [J].
Attisano, L ;
Wrana, JL .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :235-243
[6]  
BALINT EE, 2001, BRIT J CANCER, V5, P1813
[7]   Translocations involving c-myc and c-myc function [J].
Boxer, LM ;
Dang, CV .
ONCOGENE, 2001, 20 (40) :5595-5610
[8]   Co-repressors 2000 [J].
Burke, LJ ;
Baniahmad, A .
FASEB JOURNAL, 2000, 14 (13) :1876-1888
[9]   TIEG proteins join the Smads as TGF-β-regulated transcription factors that control pancreatic cell growth [J].
Cook, T ;
Urrutia, R .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (04) :G513-G521
[10]   Molecular cloning and characterization of TIEG2 reveals a new subfamily of transforming growth factor-β-inducible Sp1-like zinc finger-encoding genes involved in the regulation of cell growth [J].
Cook, T ;
Gebelein, B ;
Mesa, K ;
Mladek, A ;
Urrutia, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (40) :25929-25936