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Carboxyl-Terminal Modulator Protein Positively Acts as an Oncogenic Driver in Head and Neck Squamous Cell Carcinoma via Regulating Akt phosphorylation

机译:羧基末端调节蛋白通过调节Akt磷酸化积极发挥头颈部鳞状细胞癌的致癌驱动力。

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摘要

The exact regulatory mechanisms of carboxyl-terminal modulator protein (CTMP) and its downstream pathways in cancer have been controversial and are not completely understood. Here, we report a new mechanism of regulation of Akt serine/threonine kinase, one of the most important dysregulated signals in head and neck squamous cell carcinoma (HNSCC) by the CTMP pathway and its clinical implications. We find that HNSCC tumor tissues and cell lines had relatively high levels of CTMP expression. Clinical data indicate that CTMP expression was significantly associated with positive lymph node metastasis (OR = 3.8, P = 0.033) and correlated with poor prognosis in patients with HNSCC. CTMP was also positively correlated with Akt/GSK-3β phosphorylation, Snail up-regulation and E-cadherin down-regulation, which lead to increased proliferation and epithelial-to-mesenchymal transition, suggesting that CTMP expression results in enhanced tumorigenic and metastatic properties of HNSCC cells. Moreover, CTMP suppression restores sensitivity to cisplatin chemotherapy. Intriguingly, all the molecular responses to CTMP regulation are identical regardless of p53 status in HNSCC cells. We conclude that CTMP promotes Akt phosphorylation and functions as an oncogenic driver and prognostic marker in HNSCC irrespective of p53.
机译:羧基末端调节蛋白(CTMP)及其下游通路在癌症中的确切调控机制一直存在争议,尚未完全了解。在这里,我们报告了一种新的调节Akt丝氨酸/苏氨酸激酶的机制,该蛋白是CTMP途径在头颈部鳞状细胞癌(HNSCC)中最重要的失调信号之一,并且它具有临床意义。我们发现HNSCC肿瘤组织和细胞系具有相对较高的CTMP表达水平。临床数据表明,CTMP表达与HNSCC患者的淋巴结转移阳性显着相关(OR = 3.8,P = 0.033),并且与不良预后相关。 CTMP还与Akt /GSK-3β磷酸化,Snail上调和E-cadherin下调呈正相关,从而导致增殖增加和上皮向间充质转化,这表明CTMP表达导致增强的肿瘤发生和转移特性。 HNSCC细胞。此外,抑制CTMP可恢复对顺铂化疗的敏感性。有趣的是,无论HNSCC细胞中p53的状态如何,对CTMP调控的所有分子反应都是相同的。我们得出结论,CTMP促进Akt磷酸化,并作为HNSCC中的致癌驱动因子和预后标志物发挥作用,而与p53无关。

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