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撤稿文章:三七皂苷通过调节血管内皮生长因子抑制食管鳞状细胞癌进展 由DVL3介导的Wnt/β-连环蛋白信号通路。

Retracted Article: Panax notoginseng saponins regulate VEGF to suppress esophageal squamous cell carcinoma progression DVL3-mediated Wnt/β-catenin signaling.

作者信息

Chen Xiaoqi, Lv Zhuan, Zhang Chuanlei, Wang Xinting, Zhao Yunxia, Wang Xiao, Zheng Yuling

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Henan University of CM No. 19 Renmin Road, Jinshui District Zhengzhou Henan China

Medical Administration, The First Affiliated Hospital of Henan University of CM China.

出版信息

RSC Adv. 2020 Jan 17;10(6):3256-3265. doi: 10.1039/c9ra07830d. eCollection 2020 Jan 16.

Abstract

Panax notoginseng saponins (PNS) have recently attracted increasing attention for their anti-tumor activities. The aim of this study was to explore the functional role and underlying mechanisms of PNS on the progression of esophageal squamous cell carcinoma (ESCC). The mRNA levels of vascular endothelial growth factor (VEGF), β-catenin and dishevelled-3 (DVL3) were assessed using qRT-PCR. Western blot was performed to detect the expression levels of VEGF, β-catenin and DVL3. Cell viability and proliferation abilities were determined using MTT assay. Transwell assays were used to evaluate cell migration and invasion capacities. Our data revealed that PNS hampered the viability of ESCC cells. VEGF silencing weakened proliferation, migration and invasion in ESCC cells. Mechanistically, PNS time-dependently reduced VEGF expression and PNS hampered ESCC cell proliferation, migration and invasion through VEGF. Moreover, β-catenin and DVL3 were upregulated in ESCC tissues and cells and positively correlated with VEGF level in ESCC tissues. VEGF regulated DVL3 the Wnt/β-catenin signaling pathway in ESCC cells. Furthermore, PNS repressed DVL3 expression through VEGF in ESCC cells. Our study suggested that PNS suppressed ESCC progression at least partly through repressing VEGF the DVL3-mediated Wnt/β-catenin signaling pathway, indicating that PNS might be promising anti-tumor agents for ESCC treatment.

摘要

三七皂苷(PNS)因其抗肿瘤活性最近受到越来越多的关注。本研究的目的是探讨PNS对食管鳞状细胞癌(ESCC)进展的功能作用及潜在机制。采用qRT-PCR检测血管内皮生长因子(VEGF)、β-连环蛋白和蓬乱蛋白-3(DVL3)的mRNA水平。进行蛋白质免疫印迹法检测VEGF、β-连环蛋白和DVL3的表达水平。使用MTT法测定细胞活力和增殖能力。采用Transwell实验评估细胞迁移和侵袭能力。我们的数据显示,PNS抑制了ESCC细胞的活力。VEGF沉默减弱了ESCC细胞的增殖、迁移和侵袭。机制上,PNS能时间依赖性地降低VEGF表达,且PNS通过VEGF抑制ESCC细胞的增殖、迁移和侵袭。此外,β-连环蛋白和DVL3在ESCC组织和细胞中上调,且与ESCC组织中的VEGF水平呈正相关。VEGF在ESCC细胞中调节DVL3及Wnt/β-连环蛋白信号通路。此外,PNS在ESCC细胞中通过VEGF抑制DVL3表达。我们的研究表明,PNS至少部分通过抑制VEGF及DVL3介导的Wnt/β-连环蛋白信号通路来抑制ESCC进展,这表明PNS可能是用于ESCC治疗的有前景的抗肿瘤药物。

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