The Staufen1-dependent cell cycle regulon or how a misregulated RNA-binding protein leads to cancer

被引:12
作者
Bonnet-Magnaval, Florence [1 ]
DesGroseillers, Luc [1 ]
机构
[1] Univ Montreal, Fac Med, Dept Biochim & Med Mol, 2900 Edouard Montpetit, Montreal, PQ H3T 1J4, Canada
关键词
Staufen; post‐ transcriptional regulation; RNA regulon; cancer; cell proliferation; RNA‐ binding protein; IMMUNODEFICIENCY-VIRUS TYPE-1; KRUPPEL-LIKE FACTOR-2; MESSENGER-RNAS; STRESS GRANULES; MYOGENIC DIFFERENTIATION; TRANSCRIPTION FACTORS; SECONDARY STRUCTURES; MAMMALIAN STAUFEN; SKELETAL-MUSCLE; EMERGING ROLES;
D O I
10.1111/brv.12749
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In recent years, an increasing number of reports have linked the RNA-binding protein Staufen1 (STAU1) to the control of cell decision making. In non-transformed cells, STAU1 balances the expression of messenger RNA (mRNA) regulons that regulate differentiation and well-ordered cell division. Misregulation of STAU1 expression and/or functions changes the fragile balance in the expression of pro- and anti-proliferative and apoptotic genes and favours a novel equilibrium that supports cell proliferation and cancer development. The misregulation of STAU1 functions causes multiple coordinated modest effects in the post-transcriptional regulation of many RNA targets that code for cell cycle regulators, leading to dramatic consequences at the cellular level. The new tumorigenic equilibrium in STAU1-mediated gene regulation observed in cancer cells can be further altered by a slight increase in STAU1 expression that favours expression of pro-apoptotic genes and cell death. The STAU1-dependent cell cycle regulon is a good model to study how abnormal expression of an RNA-binding protein promotes cell growth and provides an advantageous selection of malignant cells in the first step of cancer development.
引用
收藏
页码:2192 / 2208
页数:17
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