The nuclear phosphoinositide 3-kinase/AKT pathway: a new second messenger system

被引:157
作者
Neri, LM
Borgatti, P
Capitani, S
Martelli, AM
机构
[1] Univ Ferrara, Dipartimento Morfol & Embriol, Sez Anat Umana, I-44100 Ferrara, Italy
[2] IOR, CNR, Ist Citomorfol Normale & Patol, I-40137 Bologna, Italy
[3] Univ Ferrara, Interdisciplinary Ctr Study Inflammat, I-44100 Ferrara, Italy
[4] Univ Bologna, Sch Pharm, Sez Anat, Dipartimento Sci Anat Umane & Fisiopatol Apparato, I-40126 Bologna, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2002年 / 1584卷 / 2-3期
关键词
PI3K; Akt; nucleus; signal transduction; transcription factor; cell differentiation;
D O I
10.1016/S1388-1981(02)00300-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid second messengers, particularly those derived from the polyphosphoinositide cycle, play a pivotal role in several cell signaling networks. Phosphoinositide 3-kinases (PI3Ks) generate specific mositol lipids that have been implicated in a plethora of cell functions. One of the best-characterized targets of PI3K lipid products is the serine/threonine protein kinase Akt. Recent findings have implicated Akt in cancer progression because it stimulates cell proliferation and suppresses apoptosis. Evidence accumulated over the past 15 years has highlighted the presence of an autonomous nuclear inositol lipid metabolism, and suggests that lipid molecules are important components of signaling pathways operating within the nucleus. PI3Ks, their lipid products, and Akt have also been identified at the nuclear level. In this review, we shall summarize the most updated findings about these molecules in relationship with the nuclear compartment and provide an overview of the possible mechanisms by which they regulate important cell functions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 80
页数:8
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