IPCEF1:甲状腺乳头状癌的表达模式、临床相关性和新靶点

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-21 eCollection Date: 2024-01-01 DOI:10.7150/jca.98470
Dechao Yin, Kun Wang, Junyu Zhao, Jinming Yao, Xiaofang Han, Bo Yan, Jianjun Dong, Lin Liao
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引用次数: 0

摘要

简介尽管PTC(甲状腺乳头状癌)的预后普遍良好,但它仍可能表现出侵袭性,并导致患者死亡。IPCEF1(细胞粘连蛋白交换因子 1 的相互作用蛋白)已成为癌症进展过程中与增殖和迁移相关的细胞信号传导中的一个关键角色。研究目的我们的研究旨在确定 IPCEF1 是否是 PTC 的关键基因,阐明其可能的分子机制,并最终寻找新的靶点。研究方法本研究利用四个基因表达阵列数据集和 TCGA 数据库研究 IPCEF1 在 PTC 中的作用。通过生物信息学方法实现了差异基因表达分析、生存分析、KEGG和GO富集以及免疫细胞浸润相关性分析。IHC检测了IPCEF1在PTC组织中的表达,CCK8、transwell和流式细胞术检测了PTC细胞的增殖、迁移和细胞周期。结果显示IPCEF1在PTC肿瘤组织中的表达量较低,其较低的表达量可能会导致T/N分期和DFS/PFS恶化,这可能与其调控JAK/STAT信号通路和免疫微环境(巨噬细胞和Tregs)有关。IPCEF1 可降低 PTC 细胞的增殖和迁移能力,这与我们的临床观察结果一致。此外,我们还发现 IPCEF1 的高表达水平会导致细胞周期停滞在 S 期或 G2 期,最终减少细胞的生长和增殖。结论IPCEF1 是 PTC 进展过程中的抑癌基因,通过调节免疫浸润和信号通路影响患者的生存和预后。
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IPCEF1: Expression Patterns, Clinical Correlates and New Target of Papillary Thyroid Carcinoma.

Introduction: Despite the generally favorable prognosis of PTC (Papillary Thyroid Carcinoma), it can still exhibit aggressive behavior and lead to patient mortality. IPCEF1 (interaction protein for cytohesin exchange factors 1) has emerged as a critical player in cell signaling related to proliferation and migration in cancer progression. Objective: Our research aimed to determine whether IPCEF1 is a key gene in PTC, elucidate its possible molecular mechanisms and ultimately search for new targets. Methods: This research utilized four gene expression array datasets and TCGA database to examine the role of IPCEF1 in PTC. Differential gene expression analysis, survival analysis, KEGG and GO enrichment and immune cell infiltration correlations were realized by bioinformatic methods. The expressions of IPCEF1 in PTC tissues were examined by IHC and the proliferation, migration, cell cycles of PTC cells were examined by CCK8, transwell and flow cytometry. Results: IPCEF1 had lower expression in PTC tumor tissues and its lower expression might lead to worse T/N stage and DFS/ PFS, which is perhaps related to its regulation of the JAK/STAT signaling pathway and immune microenvironment (macrophage and Tregs). IPCEF1 reduced the proliferation and migration ability of PTC cells, which is consistent with our clinical observations. Besides, we also found that high expression level of IPCEF1 lead to cell cycle arrest in the S or G2 phase, which ultimately reduced cell growth and proliferation. Conclusion: IPCEF1 is a cancer suppressor gene in the progression of PTC, influencing patient survival and prognosis through modulation of immune infiltration and signaling pathways.

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