PJA1-TGF-β信号在癌症干细胞相关性肝癌中的失调

Jian Chen, Julian A Gingold
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引用次数: 9

摘要

转化生长因子β (TGF-β)信号通路在细胞分化、干细胞调控、器官谱系和免疫抑制等方面发挥着重要作用。TGF-β信号被泛素-蛋白酶体通路负调控。虽然由缺陷的TGF-β通路引起的癌症小鼠模型清楚地证明了TGF-β的肿瘤抑制作用,但缺陷的TGF-β通路引发肝癌发展的潜在机制尚不清楚。这篇综述总结了我们最近关于TGF-β与肝癌发生的研究的主要发现,并强调了TGF-β信号传导对pja1介导的泛素化的脆弱性。TGF-β与染色质绝缘子cctc结合因子(CTCF)在TGF-β缺陷小鼠和人肝癌中通过表观遗传和转录调控肿瘤启动子基因,包括IGF2和TERT。在小鼠模型中,TGF-β调控的SPTBN1/SMAD3/CTCF复合物功能障碍可增加肝细胞癌(HCC)细胞的干细胞样特性,并促进肿瘤起始细胞的肿瘤发生。PJA1是一种新的E3泛素连接酶,是TGF-β信号传导的关键负调控因子。PJA1在HCC中过表达,足以抑制SMAD3-和sptbn1介导的TGF-β肿瘤抑制信号,促进HCC增殖。PJA1-TGF-β信号通路失调激活致癌基因,促进人类肝癌的发生。此外,E3连接酶抑制剂对PJA1的抑制可以恢复TGF-β肿瘤抑制功能并抑制肝癌的进展。这些新发现提示了通过肝癌干细胞靶向PJA1-TGF-β信号失调的潜在治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dysregulated PJA1-TGF-β signaling in cancer stem cell-associated liver cancers.

Dysregulated PJA1-TGF-β signaling in cancer stem cell-associated liver cancers.

The transforming growth factor beta (TGF-β) signaling pathway plays important roles in cell differentiation, stem cell modulation, organ lineage, and immune suppression. TGF-β signaling is negatively regulated by the ubiquitin-proteasome pathway. Although mouse models of cancer arising from a defective TGF-β pathway clearly demonstrate the tumor-suppressive role of TGF-β, the underlying mechanism by which a defective TGF-β pathway triggers liver cancer development is poorly understood. This review summarizes key findings from our recent studies connecting TGF-β to hepatic oncogenesis and highlights the vulnerability of TGF-β signaling to PJA1-mediated ubiquitination. TGF-β, together with the chromatin insulator CCCTC-binding factor (CTCF), epigenetically and transcriptionally regulate tumor promoter genes, including IGF2 and TERT, in TGF-β-defective mice and in human liver cancers. Dysfunction of the TGF-β-regulated SPTBN1/SMAD3/CTCF complex increases stem cell-like properties in hepatocellular carcinoma (HCC) cells and enhances tumorigenesis in tumor-initiating cells in a mouse model. PJA1, a novel E3 ubiquitin ligase, is a key negative regulator of TGF-β signaling. PJA1 overexpression is detected in HCCs and is sufficient to suppress SMAD3- and SPTBN1-mediated TGF-β tumor suppressor signaling, promoting HCC proliferation. Dysregulated PJA1-TGF-β signaling activates oncogenic genes and promotes tumorigenesis in human liver cancers. In addition, inhibition of PJA1 by treatment with E3 ligase inhibitors restores TGF-β tumor-suppressor function and suppresses liver cancer progression. These new findings suggest potential therapeutic avenues for targeting dysregulated PJA1-TGF-β signaling via cancer stem cells in liver cancers.

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