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JWA通过不同的丝裂原活化蛋白激酶信号通路调控人食管鳞状细胞癌和人食管细胞。

JWA regulates human esophageal squamous cell carcinoma and human esophageal cells through different mitogen-activated protein kinase signaling pathways.

作者信息

Lin Jie, Ma Tieliang, Jiang Xiaodong, Ge Zhijun, Ding Weiliang, Wu Yuanyuan, Jiang Guojun, Feng Jiake, Cui Guoxing, Tan Yongfei

机构信息

Department of Cardiac and Thoracic Surgery, Affiliated Yixing People's Hospital, Jiangsu University, Yixing, Jiangsu 214200, P.R. China.

Central Laboratory, Affiliated Yixing People's Hospital, Jiangsu University, Yixing, Jiangsu 214200, P.R. China.

出版信息

Exp Ther Med. 2014 Jun;7(6):1767-1771. doi: 10.3892/etm.2014.1650. Epub 2014 Mar 28.

Abstract

The aim of the present study was to investigate whether the JWA gene regulates the proliferation, migration and invasion of human esophageal squamous cell carcinoma (ESCC) and normal human esophageal cell lines through mitogen-activated protein kinase (MAPK) signal transduction pathways. The role of JWA in proliferation, migration, invasion and apoptosis was investigated in the Eca109 human ESCC and HET-1A normal human esophageal cell lines via transfection with JWA-small interfering (si)RNA. Western blot analysis was conducted to observe the effect of JWA on apoptosis and the regulatory effect of JWA on proliferation was determined using a thiazolyl blue tetrazolium bromide (MTT) assay. Cellular migration and invasion were analyzed via a Transwell assay. In addition, the expression levels of extracellular signal-regulated protein kinases 1 and 2 (ERK1/2), c-Jun N-terminal kinase (JNK) and p38 MAPK following JWA-siRNA transfection were detected by western blot analysis and compared with those of untreated cells. The downregulation of JWA protein decreased apoptosis and increased the proliferation, migration and invasion of the Eca109 and HET-1A cell lines. In the Eca109 cell line, the expression levels of phosphorylated (p)-ERK1/2 and p-JNK, but not those of p-p38, decreased significantly in the JWA siRNA group compared with those in the control groups. However, in the HET-1A cell line, JWA-siRNA transfection significantly inhibited the expression of p-p38 and demonstrated no effect on the expression levels of p-ERK1/2 and p-JNK. In conclusion, the JWA gene may regulate the ESCC and human esophageal cell lines through MAPK signaling pathways via different regulatory mechanisms.

摘要

本研究的目的是探讨JWA基因是否通过丝裂原活化蛋白激酶(MAPK)信号转导通路调节人食管鳞状细胞癌(ESCC)和正常人食管细胞系的增殖、迁移和侵袭。通过用JWA小干扰(si)RNA转染,在Eca109人ESCC和HET-1A正常人食管细胞系中研究JWA在增殖、迁移、侵袭和凋亡中的作用。进行蛋白质免疫印迹分析以观察JWA对凋亡的影响,并使用噻唑蓝四氮唑溴盐(MTT)法测定JWA对增殖的调节作用。通过Transwell试验分析细胞迁移和侵袭。此外,通过蛋白质免疫印迹分析检测JWA-siRNA转染后细胞外信号调节蛋白激酶1和2(ERK1/2)、c-Jun氨基末端激酶(JNK)和p38 MAPK的表达水平,并与未处理细胞进行比较。JWA蛋白的下调减少了凋亡,并增加了Eca109和HET-1A细胞系的增殖、迁移和侵袭。在Eca109细胞系中,与对照组相比,JWA siRNA组中磷酸化(p)-ERK1/2和p-JNK的表达水平显著降低,但p-p38的表达水平未降低。然而,在HET-1A细胞系中,JWA-siRNA转染显著抑制了p-p38的表达,并且对p-ERK1/2和p-JNK的表达水平没有影响。总之,JWA基因可能通过不同的调节机制,经MAPK信号通路调节ESCC和人食管细胞系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60fe/4043574/b45025ab9439/ETM-07-06-1767-g00.jpg

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