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衰老与癌症中的FOXO转录因子。

FOXO transcription factors in ageing and cancer.

作者信息

Greer E L, Brunet A

机构信息

Department of Genetics, Stanford University, Stanford, CA 94305, USA.

出版信息

Acta Physiol (Oxf). 2008 Jan;192(1):19-28. doi: 10.1111/j.1748-1716.2007.01780.x.

Abstract

Ageing is associated with an increased onset of cancer. Understanding the molecular mechanisms that underlie the age dependency of cancer will have important implications for preventing and treating this pathology. The signalling pathway connecting insulin and FOXO transcription factors provides the most compelling example for a conserved genetic pathway at the interface between ageing and cancer. FOXO transcription factors (FOXO) promote longevity and tumour suppression. FOXO transcription factors are directly phosphorylated in response to insulin/growth factor signalling by the protein kinase Akt, thereby causing their sequestration in the cytoplasm. In the absence of insulin/growth factors, FOXO factors translocate to the nucleus where they trigger a range of cellular responses, including resistance to oxidative stress, a phenotype highly coupled with lifespan extension. FOXO factors integrate stress stimuli via phosphorylation, acetylation and mono-ubiquitination of a series of regulatory sites. Understanding how FOXO proteins integrate environmental conditions to control specific gene expression programmes will be pivotal in identifying ways to slow the onset of cancer in ageing individuals.

摘要

衰老与癌症发病率的增加有关。了解癌症年龄依赖性背后的分子机制对于预防和治疗这种疾病具有重要意义。连接胰岛素和FOXO转录因子的信号通路为衰老与癌症之间界面上保守的遗传通路提供了最有说服力的例子。FOXO转录因子(FOXO)促进长寿和肿瘤抑制。FOXO转录因子在胰岛素/生长因子信号传导的作用下被蛋白激酶Akt直接磷酸化,从而导致它们被隔离在细胞质中。在缺乏胰岛素/生长因子的情况下,FOXO因子转移到细胞核,在那里它们引发一系列细胞反应,包括对氧化应激的抗性,这是一种与寿命延长高度相关的表型。FOXO因子通过一系列调节位点的磷酸化、乙酰化和单泛素化整合应激刺激。了解FOXO蛋白如何整合环境条件以控制特定基因表达程序对于确定延缓衰老个体癌症发病的方法至关重要。

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