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[CK2α通过PI3K/Akt/GSK-3β信号通路调控肺腺癌A549细胞系的转移和迁移]

[CK2α Regulates the Metastases and Migration of Lung Adenocarcinoma 
A549 Cell Line through PI3K/Akt/GSK-3β Signal Pathway].

作者信息

Wu Aibing, Li Mingchun, Mai Zongjiong, Li Shujun, Yang Zhixiong

机构信息

Department of Oncology, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524000, China.

Department of Oncology, Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2017 Apr 20;20(4):233-238. doi: 10.3779/j.issn.1009-3419.2017.04.11.

Abstract

BACKGROUND

Lung cancer is the leading cancer-related death worldwide. Patients with lung cancer mainly died of tumor metastasis and invasion. Protein kinase CK2 is an ubiquitous serine/threonine protein kinase and is frequently upregulated in various human tumors. This study aims to explore the effect and molecular mechanism of the invasion and migration of lung adenocarcinoma A549 cells after knock-down of CK2α expression.

METHODS

The pSilencerTM 4.1-siCK2α-eGFP of lentiviral-mediated shRNA was constructed. The expression of CK2α was knock-downed, and a stable A549 cell line was established. The invasion and migration of A549 cell line was detected through Transwell and Boyden chamber assays. The protein expression of the PI3K/Akt signaling pathway and mesenchymal-to-epithelial transition (EMT) was evaluated using Western blot analysis.

RESULTS

The invasion and migration of A549 cells were significantly inhibited after the knockdown of CK2α expression compared with that in the control group. p-PTEN, Akt, p-Akt473, p-Akt308, p-PDK1, p-c-Raf, and p-GSK-3β were significantly downregulated, whereas PTEN was upregulated. Moreover, vimentin, β-catenin, Snail, MMP2, and MMP9 were significantly downregulated after reducing the CK2α expression.

CONCLUSIONS: CK2α might regulate the invasion and migration of A549 cells through the PI3K/Akt/GSK-3β/Snail signaling pathway, which controls EMT in lung adenocarcinoma.
.

摘要

背景

肺癌是全球癌症相关死亡的主要原因。肺癌患者主要死于肿瘤转移和侵袭。蛋白激酶CK2是一种普遍存在的丝氨酸/苏氨酸蛋白激酶,在各种人类肿瘤中经常上调。本研究旨在探讨敲低CK2α表达后对肺腺癌A549细胞侵袭和迁移的影响及分子机制。

方法

构建慢病毒介导的shRNA的pSilencerTM 4.1-siCK2α-eGFP。敲低CK2α的表达,并建立稳定的A549细胞系。通过Transwell和Boyden小室实验检测A549细胞系的侵袭和迁移。使用蛋白质印迹分析评估PI3K/Akt信号通路和间充质-上皮转化(EMT)的蛋白表达。

结果

与对照组相比,敲低CK2α表达后A549细胞的侵袭和迁移受到显著抑制。p-PTEN、Akt、p-Akt473、p-Akt308、p-PDK1、p-c-Raf和p-GSK-3β显著下调,而PTEN上调。此外,降低CK2α表达后波形蛋白、β-连环蛋白、Snail、MMP2和MMP9显著下调。

结论

CK2α可能通过PI3K/Akt/GSK-3β/Snail信号通路调节A549细胞的侵袭和迁移,该信号通路控制肺腺癌中的EMT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ec1/5999677/d30abff01095/zgfazz-20-4-233-1.jpg

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