白血病抑制因子的调控。

Xuetian Yue, Lihua Wu, Wenwei Hu
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引用次数: 61

摘要

白血病抑制因子(Leukemia inhibitory factor, LIF)是一种分泌性细胞因子,在诱导白血病细胞分化、炎症反应、神经元发育、胚胎着床、干细胞自我更新和肿瘤进展等一系列生物学过程中发挥重要作用。LIF主要通过激活和调控JAK/STAT3、AKT、EKR1/2和mTOR信号通路发挥其生物学功能。在不同的组织/细胞类型中,在不同的条件下,LIF的表达水平受到许多不同因素的调控。例如,雌激素和p53是着床期子宫组织高LIF产生的重要调节因子。在实体肿瘤中,缺氧在LIF过表达中起关键作用。许多细胞因子,包括IL-6, IL-1β,也可以诱导LIF的表达和产生。本文就目前对LIF在不同条件下的转录调控的认识进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The regulation of leukemia inhibitory factor.
Leukemia inhibitory factor (LIF), a secreted cytokine, plays an important role in a wide array of biological processes including inducing differentiation of leukemia cell, inflammatory response, neuronal development, embryonic implantation, stem cell self-renewal and cancer progression, etc. LIF exerts its biological functions mainly through the activation and regulation of JAK/STAT3, AKT, EKR1/2 and mTOR signal pathways. The expression levels of LIF are regulated by many different factors under different conditions in different tissue/cell types. For example, estrogen and p53 are important regulators for the high LIF production in uterine tissues at the implantation stage. Hypoxia plays a critical role in LIF overexpression in solid tumors. Many cytokines, including IL-6, IL-1β, can also induce the LIF expression and production. In this review, we summarize the current understanding on the transcriptional regulation of LIF under various conditions.
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