PTEN公司
PI3K/AKT/mTOR通路
张力素
蛋白激酶B
癌症研究
MAPK/ERK通路
生物
信号转导
细胞生物学
作者
Linda S. Steelman,Stephen L. Abrams,Jarrett T. Whelan,F. E. Bertrand,D E Ludwig,Jörg Bäsecke,Massimo Libra,Franca Stivala,Michèle Milella,Agostino Tafuri,Paolo Lunghi,Antonio Bonati,Alberto M. Martelli,James A. McCubrey
出处
期刊:Leukemia
[Springer Nature]
日期:2008-03-13
卷期号:22 (4): 686-707
被引量:359
摘要
Mutations and chromosomal translocations occur in leukemic cells that result in elevated expression or constitutive activation of various growth factor receptors and downstream kinases. The Raf/MEK/ERK, PI3K/PTEN/Akt/mTOR and Jak/STAT pathways are often activated by mutations in upstream genes. The Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR pathways are regulated by upstream Ras that is frequently mutated in human cancer. Recently, it has been observed that the FLT-3 and Jak kinases and the phosphatase and tensin homologue deleted on chromosome 10 (PTEN) phosphatase are also frequently mutated or their expression is altered in certain hematopoietic neoplasms. Many of the events elicited by the Raf/MEK/ERK, PI3K/PTEN/Akt/mTOR and Jak/STAT pathways have direct effects on survival pathways. Aberrant regulation of the survival pathways can contribute to uncontrolled cell growth and lead to leukemia. In this review, we describe the Raf/MEK/ERK, PI3K/PTEN/Akt/mTOR and Jak/STAT signaling cascades and summarize recent data regarding the regulation and mutation status of these pathways and their involvement in leukemia.
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