TPT1/ TCTP-regulated pathways in phenotypic reprogramming

被引:111
作者
Amson, Robert [1 ]
Pece, Salvatore [2 ,3 ,4 ]
Marine, Jean-Christophe [5 ,6 ]
Di Fiore, Pier Paolo [2 ,3 ,4 ]
Telerman, Adam [1 ]
机构
[1] Ecole Normale Super, LBPA, CNRS, UMR 8113, F-94235 Cachan, France
[2] Ist FIRC Oncol Mol, I-20139 Milan, Italy
[3] Ist Europeo Oncol, I-20141 Milan, Italy
[4] Univ Milan, Dipartimento Med Chirurg & Odontoiatria, I-20122 Milan, Italy
[5] VIB, Ctr Biol Dis, Lab Mol Canc Biol, B-3000 Louvain, Belgium
[6] Katholieke Univ Leuven, Lab Mol Canc Biol, B-3000 Louvain, Belgium
关键词
p53; MDM2; tumor reversion; stem cells; CONTROLLED TUMOR PROTEIN; HISTAMINE-RELEASING FACTOR; TRANSLATIONAL CONTROL; NUCLEOTIDE EXCHANGE; EXOSOME SECRETION; P53; GROWTH; MOUSE; IDENTIFICATION; APOPTOSIS;
D O I
10.1016/j.tcb.2012.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Evolutionary conserved and pleiotropic, the TPT1/TCTP gene (translationally controlled tumor protein, also called HRF, fortilin), encodes a highly structured mRNA shielded by ribonucleoproteins and closely resembling viral particles. This mRNA activates, as do viruses, protein kinase R (PKR). The TPT1/TCTP protein is structurally similar to mRNA-helicases and MSS4. TPT1/TCTP has recently been identified as a prognostic factor in breast cancer and a critical regulator of the tumor suppressor p53 and of the cancer stem cell (SC) compartment. Emerging evidence indicates that TPT1/TCTP is key to phenotypic reprogramming, as shown in the process of tumor reversion and possibly in pluripotency. We provide here an overview of these diverse functions of TPT1/TCTP.
引用
收藏
页码:37 / 46
页数:10
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