A novel signaling network as a critical rheostat for the biology and maintenance of the normal stem cell and the cancer-initiating cell

被引:47
|
作者
Ito, Keisuke [1 ,2 ]
Bernardi, Rosa [1 ,2 ,3 ]
Pandolfi, Pier Paolo [1 ,2 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Canc Genet Program, Sch Med, Boston, MA 02215 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Dept Med, Sch Med, Boston, MA 02215 USA
[3] Ist Sci San Raffaele, I-20132 Milan, Italy
关键词
CHRONIC MYELOGENOUS LEUKEMIA; FOXO TRANSCRIPTION FACTORS; CHRONIC MYELOID-LEUKEMIA; TUMOR-SUPPRESSOR; IMATINIB MESYLATE; SELF-RENEWAL; BONE-MARROW; PTEN; PML; MTOR;
D O I
10.1016/j.gde.2009.01.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent advances from our own group and others have defined a novel PML/PTEN/Akt/mTOR/FoxO signaling network, and highlighted its critical importance in oncogenesis as well as in the functional regulation of normal stem cell and cancer-initiating cell (CIC) biology. These findings are of great importance in cancer therapy in view of the fact that this network is amenable to pharmacological modulation at multiple levels. The integrated analysis of these data allows us to propose a new provocative working model whereby the aberrant superactivation of Akt/mTOR signaling elicits built-in cellular fail-safe mechanisms that could be effectively utilized for cancer treatment to extinguish the CICs pool. In this review, we will discuss these recent findings, this working model, and their therapeutic implications.
引用
收藏
页码:51 / 59
页数:9
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