Molecular mechanisms of tumor suppression by LKB1

被引:89
作者
Vaahtomeri, Kari
Makela, Tomi P. [1 ]
机构
[1] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
LKB1; Lung adenocarcinoma; Cervical cancer; Peutz-Jeghers syndrome; AMPK; p53; PEUTZ-JEGHERS-SYNDROME; ACTIVATED PROTEIN-KINASE; LUNG-CANCER; SOMATIC MUTATIONS; DEPENDENT REGULATION; LKB1-AMPK PATHWAY; SPINDLE FORMATION; ELEGANS EMBRYOS; DROSOPHILA LKB1; GROWTH ARREST;
D O I
10.1016/j.febslet.2010.12.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The LKB1 tumor suppressor gene is frequently mutated in sporadic lung adenocarcinomas and cervical cancers and germline mutations are causative for Peutz-Jeghers syndrome characterized by gastrointestinal polyposis. The intracellular LKB1 kinase is implicated in regulating polarity, metabolism, cell differentiation, and proliferation - all functions potentially contributing to tumor suppression. LKB1 acts as an activating kinase of at least 14 kinases mediating LKB1 functions in a complex signaling network with partial overlaps. Regulation of the LKB1 signaling network is highly context dependent, and spatially organized in various cellular compartments. Also the mechanisms by which LKB1 activity suppresses tumorigenesis is context dependent, where recent observations are providing hints on the molecular mechanisms involved. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:944 / 951
页数:8
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