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转录因子 GATA6 通过抑制 BMP 基因表达来实现结肠腺瘤干细胞的自我更新。

The transcription factor GATA6 enables self-renewal of colon adenoma stem cells by repressing BMP gene expression.

机构信息

Institute for Research in Biomedicine (IRB Barcelona), 08028 Barcelona, Spain.

1] Institute for Research in Biomedicine (IRB Barcelona), 08028 Barcelona, Spain [2].

出版信息

Nat Cell Biol. 2014 Jul;16(7):695-707. doi: 10.1038/ncb2992. Epub 2014 Jun 22.

Abstract

Aberrant activation of WNT signalling and loss of BMP signals represent the two main alterations leading to the initiation of colorectal cancer (CRC). Here we screen for genes required for maintaining the tumour stem cell phenotype and identify the zinc-finger transcription factor GATA6 as a key regulator of the WNT and BMP pathways in CRC. GATA6 directly drives the expression of LGR5 in adenoma stem cells whereas it restricts BMP signalling to differentiated tumour cells. Genetic deletion of Gata6 from mouse colon adenomas increases the levels of BMP factors, which signal to block self-renewal of tumour stem cells. In human tumours, GATA6 competes with β-catenin/TCF4 for binding to a distal regulatory region of the BMP4 locus that has been linked to increased susceptibility to development of CRC. Hence, GATA6 creates an environment permissive for CRC initiation by lowering the threshold of BMP signalling required for tumour stem cell expansion.

摘要

WNT 信号通路的异常激活和 BMP 信号的丢失是导致结直肠癌(CRC)发生的两个主要改变。在这里,我们筛选了维持肿瘤干细胞表型所需的基因,并鉴定出锌指转录因子 GATA6 是 CRC 中 WNT 和 BMP 通路的关键调节因子。GATA6 直接驱动腺瘤干细胞中 LGR5 的表达,而将 BMP 信号限制在分化的肿瘤细胞中。从小鼠结肠腺瘤中遗传缺失 Gata6 会增加 BMP 因子的水平,这些因子发出信号以阻止肿瘤干细胞的自我更新。在人类肿瘤中,GATA6 与 β-catenin/TCF4 竞争结合 BMP4 基因座的远端调控区域,该区域与 CRC 易感性增加有关。因此,GATA6 通过降低肿瘤干细胞扩增所需的 BMP 信号阈值,为 CRC 的发生创造了一个有利的环境。

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