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Lkb1/AMPK信号通路在造血干细胞和白血病中的作用。

The role of the Lkb1/AMPK pathway in hematopoietic stem cells and Leukemia.

作者信息

Saito Yusuke, Nakada Daisuke

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.

出版信息

Crit Rev Oncog. 2014;19(5):383-97. doi: 10.1615/critrevoncog.2014011765.

Abstract

The liver kinase B1 (Lkb1)/AMP-activated protein kinase (AMPK) pathway maintains metabolic homeostasis of cells by promoting catabolism and inhibiting anabolism. Activation of this pathway induces tumor suppressors, including p53, and leads to inhibition of the mammalian target of rapamycin pathway, which often is overactivated in multiple cancers. Thus, the Lkb1/AMPK pathway suppresses cancer by negatively regulating cell proliferation. However, recent studies of mouse hematopoietic stem cells (HSCs) revealed that Lkb1 is critical for maintaining HSCs, rather than limiting their proliferation. Furthermore, the role of AMPK in cancer cells has remained elusive. Outstanding questions concern the role of the Lkb1/AMPK pathway in regulating the metabolism and proliferation of cancer cells within a physiological setting. This review focuses on the function of the Lkb1/AMPK pathway in HSCs and leukemia and provides an overview of the therapeutic strategies aimed at targeting this pathway in cancer.

摘要

肝脏激酶B1(Lkb1)/AMP激活的蛋白激酶(AMPK)通路通过促进分解代谢和抑制合成代谢来维持细胞的代谢稳态。该通路的激活可诱导包括p53在内的肿瘤抑制因子,并导致雷帕霉素哺乳动物靶标通路受到抑制,而该通路在多种癌症中常常过度激活。因此,Lkb1/AMPK通路通过负向调节细胞增殖来抑制癌症。然而,最近对小鼠造血干细胞(HSC)的研究表明,Lkb1对维持造血干细胞至关重要,而非限制其增殖。此外,AMPK在癌细胞中的作用仍不明确。悬而未决的问题涉及Lkb1/AMPK通路在生理环境中调节癌细胞代谢和增殖的作用。本综述聚焦于Lkb1/AMPK通路在造血干细胞和白血病中的功能,并概述了旨在靶向该通路治疗癌症的策略。

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