首页> 美国卫生研究院文献>Oncotarget >Inflammatory related gene IKKα IKKβ IKKγ cooperates to determine liver cancer stem cells progression by altering telomere via heterochromatin protein 1-HOTAIR axis
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Inflammatory related gene IKKα IKKβ IKKγ cooperates to determine liver cancer stem cells progression by altering telomere via heterochromatin protein 1-HOTAIR axis

机译:炎症相关基因IKKαIKKβIKKγ通过异染色质蛋白1-HOTAIR轴共同改变端粒共同确定肝癌干细胞的进程

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摘要

Cancer stem cells are associated with tumor recurrence. IKK is a protein kinase that is composed of IKKα, IKKβ, IKKγ. Herein, we demonstrate that IKKα plus IKKβ promoted and IKKγ inhibited liver cancer stem cell growth in vitro and in vivo. Mechanistically, IKKα plus IKKβ enhanced and IKKγ inhibited the interplay among HP1α, HP1β and HP1γ that competes for the interaction among HP1α, SUZ12, HEZ2. Therefore, IKKα plus IKKβ inhibited and IKKγ enhanced the activity of H3K27 methyltransferase SUZ12 and EZH2, which methylates H3K27 immediately sites on HOTAIR promoter region. Therefore, IKKα plus IKKβ increased and IKKγ decreased the HOTAIR expression. Strikingly, IKKα plus IKKβ decreases and IKKγ increases the HP1α interplays with DNA methyltransferase DNMT3b, which increases or decreases TERRA promoter DNA methylation. Thus IKKα plus IKKβ reduces and IKKγ increases to recruit TRF1 and RNA polymerase II deposition and elongation on the TERRA promoter locus, which increases or decreases TERRA expression. Furthermore, IKKα plus IKKβ decreases/increases and IKKγ increases/decreases the interplay between TERT and TRRRA/between TERT and TREC. Ultimately, IKKα plus IKKβ increases and IKKγ decreases the telomerase activity. On the other hand, at the telomere locus, IKKα plus IKKβ increases/drcreases and IKKγ decreases/increases TRF2, POT1, pPOT1, Exo1, pExo1, SNM1B, pSNM1B/CST-AAF binding, which keep active telomere regulatory genes and poised for telomere length. Strikingly, HOTAIR is required for IKKα plus IKKβ and IKKγ to control telomerase activity and telomere length. These observations suggest that HOTAIR operates the action of IKKα, IKKβ, IKKγ in liver cancer stem cells. This study provides a novel basis to elucidate the oncogenic action of IKKα, IKKβ, IKKγ and prompts that IKKα, IKKβ, IKKγ cooperate to HOTAR to be used as a novel therapeutic targets for liver cancer.
机译:癌症干细胞与肿瘤复发有关。 IKK是由IKKα,IKKβ,IKKγ组成的蛋白激酶。在本文中,我们证明了IKKα加IKKβ在体外和体内均可促进和抑制IKKγ抑制肝癌干细胞的生长。从机理上讲,IKKα加IKKβ增强,IKKγ抑制HP1α,HP1β和HP1γ之间的相互作用,从而竞争HP1α,SUZ12,HEZ2之间的相互作用。因此,IKKα加IKKβ抑制了IKKγ的活性,增强了H3K27甲基转移酶SUZ12和EZH2的活性,使H3K27甲基化并直接位于HOTAIR启动子区域。因此,IKKα加IKKβ增加,而IKKγ降低HOTAIR表达。令人惊讶的是,IKKα加IKKβ减少,IKKγ增加HP1α与DNA甲基转移酶DNMT3b的相互作用,从而增加或减少TERRA启动子DNA甲基化。因此,IKKα加IKKβ减少,IKKγ增加,以募集TRF1和RNA聚合酶II在TERRA启动子基因座上的沉积和延伸,从而增加或减少TERRA表达。此外,IKKα加IKKβ减少/增加,而IKKγ增加/减少TERT和TRRRA之间/ TERT和TREC之间的相互作用。最终,IKKα加IKKβ增加,而IKKγ降低端粒酶活性。另一方面,在端粒位点,IKKα加IKKβ增加/减少,IKKγ减少/增加TRF2,POT1,pPOT1,Exo1,pExo1,SNM1B,pSNM1B / CST-AAF的结合,从而保持活性端粒调控基因并为端粒蓄势长度。令人惊讶的是,IKKα加上IKKβ和IKKγ需要HOTAIR来控制端粒酶活性和端粒长度。这些观察结果表明,HOTAIR在肝癌干细胞中发挥了IKKα,IKKβ,IKKγ的作用。该研究为阐明IKKα,IKKβ,IKKγ的致癌作用提供了新的依据,并提示IKKα,IKKβ,IKKγ与HOTAR协同作用,可作为肝癌的新型治疗靶标。

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