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Human telomerase reverse transcriptase (hTERT) promotes gastric cancer invasion through cooperating with c-Myc to upregulate heparanase expression

机译:人类端粒酶逆转录酶(hTERT)通过与c-Myc协同上调肝素酶表达促进胃癌侵袭

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摘要

Human telomerase reverse transcriptase (hTERT) is a central regulator of multiple hallmarks of tumors. However, the potential roles of hTERT in tumor invasion and metastasis and the underlying molecular mechanisms remain poorly understood. Here, we found that the expression of hTERT in gastric cancer (GC) was significantly associated with an advanced TNM stage, lymphatic metastasis. Survival analysis identified hTERT as an independent prognostic factor for survival of GC patients. hTERT promoted the invasion and metastasis of GC cells by binding to c-Myc and recruiting the complex to heparanase promoter to upregulate heparanase expression. In addition, our data demonstrated that hTERT activated Wnt/β-catenin signaling to promote c-Myc expression which could in turn activate hTERT transcription and expression, suggesting a positive feedback regulation in GC progression. Consistently, c-Myc and heparanase expression was positively correlated with hTERT levels, and was also an independent predictor of metastasis and survival. Collectively, our data provide a novel molecular mechanism for hTERT in promotion of GC invasion and metastasis, and highlight the molecular etiology and clinical significance of hTERT in GC progression. Targeting hTERT may represent a new therapeutic strategy to improve therapy and survival of GC patients.
机译:人端粒酶逆转录酶(hTERT)是肿瘤的多个标志的中央调节器。然而,hTERT在肿瘤侵袭和转移中的潜在作用以及潜在的分子机制仍然知之甚少。在这里,我们发现hTERT在胃癌(GC)中的表达与TNM晚期,淋巴转移密切相关。生存分析确定hTERT是GC患者生存的独立预后因素。 hTERT通过与c-Myc结合并将复合物募集到乙酰肝素酶启动子上调肝素酶表达,从而促进了GC细胞的侵袭和转移。此外,我们的数据表明hTERT激活Wnt /β-catenin信号来促进c-Myc表达,这又可以激活hTERT转录和表达,表明在GC进程中有积极的反馈调控。一致地,c-Myc和乙酰肝素酶的表达与hTERT水平呈正相关,并且还是转移和生存的独立预测因子。总的来说,我们的数据为hTERT促进GC侵袭和转移提供了新的分子机制,并突出了hTERT在GC进展中的分子病因和临床意义。靶向hTERT可能代表一种新的治疗策略,以改善GC患者的治疗和生存。

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