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PCGF3 通过 PI3K/AKT 信号通路促进非小细胞肺癌细胞的增殖和迁移。

PCGF3 promotes the proliferation and migration of non-small cell lung cancer cells via the PI3K/AKT signaling pathway.

机构信息

Department of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.

Department of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China; Department of Pathology, Cancer Research Laboratory, Chengde Medical College, Hebei, China.

出版信息

Exp Cell Res. 2021 Mar 15;400(2):112496. doi: 10.1016/j.yexcr.2021.112496. Epub 2021 Jan 21.

Abstract

The Polycomb Group Ring Finger 3 (PCGF3) protein has been reported to be significantly upregulated in pancreatic islet tumors and related to signal transduction; however, its detailed mechanisms and biological roles in other tumors, including non-small cell lung cancer (NSCLC), remain unclear. This study investigated the function of PCGF3 in NSCLC and further elucidated its mechanism of action. The immunohistochemical analysis of 86 selected lung cancer tissues revealed that PCGF3 was highly expressed in NSCLC tissues and positively correlated with lymph node metastasis and p-TNM staging. Additionally, PCGF3 promoted cell proliferation in lung cancer by regulating CyclinB1, CyclinD1, and CDK4 expression, and also promoting their migration by regulating RhoA, RhoC, and CDC42. Furthermore, PCGF3 affected both the proliferation and migration of lung cancer cells by regulating the PI3K/AKT pathway, as verified by inhibiting this pathway using LY294002. The findings of this study suggested that PCGF3 is associated with poor prognosis in patients with NSCLC and could therefore be an important biomarker for treating and preventing NSCLC.

摘要

多梳抑制复合物环指蛋白 3(PCGF3)蛋白已被报道在胰岛肿瘤中显著上调,并与信号转导有关;然而,其在其他肿瘤(包括非小细胞肺癌(NSCLC))中的详细机制和生物学作用仍不清楚。本研究探讨了 PCGF3 在 NSCLC 中的功能,并进一步阐明了其作用机制。对 86 例选定的肺癌组织进行免疫组织化学分析表明,PCGF3 在 NSCLC 组织中高表达,与淋巴结转移和 p-TNM 分期呈正相关。此外,PCGF3 通过调节 CyclinB1、CyclinD1 和 CDK4 的表达促进肺癌细胞增殖,并通过调节 RhoA、RhoC 和 CDC42 促进其迁移。此外,PCGF3 通过调节 PI3K/AKT 通路影响肺癌细胞的增殖和迁移,这一点通过使用 LY294002 抑制该通路得到了验证。本研究的结果表明,PCGF3 与 NSCLC 患者的不良预后相关,因此可能是治疗和预防 NSCLC 的重要生物标志物。

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