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LncRNA ZEB2-AS1 通过激活 Wnt/β-catenin 通路促进胃癌的发生。

LncRNA ZEB2-AS1 contributes to the tumorigenesis of gastric cancer via activating the Wnt/β-catenin pathway.

机构信息

Department of Clinical Laboratory, Chang'an Hospital, Xi'an, 710016, Shaanxi, People's Republic of China.

Department of Clinical Laboratory, Ankang Municipality of Traditional Chinese Medicine Hospital, No. 47, East Bashan Road, Ankang, 725000, Shaanxi, People's Republic of China.

出版信息

Mol Cell Biochem. 2019 Jun;456(1-2):73-83. doi: 10.1007/s11010-018-03491-7. Epub 2019 Jan 11.

Abstract

Studies have shown that long noncoding RNA Zinc finger E-box-binding homeobox 2 antisense RNA 1 (ZEB2-AS1) is involved in the progression of lung cancer, bladder cancer, and hepatocellular carcinoma. However, its role in the pathogenesis of gastric cancer remains unknown. The Wnt/β-catenin pathway contributes to the development of gastric cancer. ZEB2-AS1 expression was firstly detected in the gastric carcinoma tissue samples as well as in gastric cancer cells. Knockdown of ZEB2-AS1 was performed by ZEB2-AS1-shRNA, and the viability, migration, invasion, and apoptosis of gastric cancer cells were determined by CCK-8, scratch assay, transwell, and flow cytometry, respectively. Furthermore, levels of Ki-67, PCNA, VEGF, MMP9, epithelial-mesenchymal transition (EMT) markers (E-cadherin, Vimentin and ZEB2), cleaved caspase 3/8/9 and PARP, active β-catenin, c-Myc, cyclinD1, and AXIN2 were assayed by Western blot or real-time PCR. Additionally, the role and mechanism of ZEB2-AS1 were confirmed in a xenograft nude mouse model. We found ZEB2-AS1 expression was increased in gastric carcinoma samples, and it was correlated with tumor progression. Also, its expression was elevated in gastric cancer cells. Knockdown of ZEB2-AS1 reduced the proliferation, migration, invasion, and EMT, but increased the apoptosis of gastric carcinoma cells. Furthermore, ZEB2-AS1 downregulation remarkably suppressed the expression of Ki-67, PCNA, VEGF and MMP9, and the activation of Wnt/β-catenin signaling, whereas elevated the levels of cleaved caspase 3/8/9 and PARP in gastric cancer cells. And ZEB2 overexpression reversed the effects of ZEB2-AS1 downregulation on the proliferation, EMT and inactivation of Wnt/β-catenin signaling. Additionally, ZEB2-AS1 knockdown inhibited tumor growth, Ki-67 staining, and the expression of VEGF, MMP9, active β-catenin, c-Myc, cyclinD1, and AXIN2 in mice. In conclusion, ZEB2-AS1 promotes the tumorigenesis of gastric carcinoma that is related to the upregulation of ZEB2 and the activation of the Wnt/β-catenin pathway.

摘要

研究表明,长非编码 RNA 锌指 E 框结合同源盒 2 反义 RNA 1(ZEB2-AS1)参与了肺癌、膀胱癌和肝癌的进展。然而,其在胃癌发病机制中的作用尚不清楚。Wnt/β-catenin 通路促进了胃癌的发展。ZEB2-AS1 的表达最初在胃癌组织样本以及胃癌细胞中被检测到。通过 ZEB2-AS1-shRNA 敲低 ZEB2-AS1,然后通过 CCK-8、划痕实验、Transwell 和流式细胞术分别测定胃癌细胞的活力、迁移、侵袭和凋亡。此外,通过 Western blot 或实时 PCR 测定 Ki-67、PCNA、VEGF、MMP9、上皮-间充质转化(EMT)标志物(E-钙粘蛋白、波形蛋白和 ZEB2)、cleaved caspase 3/8/9 和 PARP、活性 β-catenin、c-Myc、cyclinD1 和 AXIN2 的水平。此外,在异种移植裸鼠模型中验证了 ZEB2-AS1 的作用和机制。我们发现 ZEB2-AS1 在胃癌样本中的表达增加,并且与肿瘤进展相关。此外,其在胃癌细胞中的表达上调。敲低 ZEB2-AS1 可降低胃癌细胞的增殖、迁移、侵袭和 EMT,但增加其凋亡。此外,ZEB2-AS1 下调显著抑制 Ki-67、PCNA、VEGF 和 MMP9 的表达和 Wnt/β-catenin 信号的激活,而在胃癌细胞中上调 cleaved caspase 3/8/9 和 PARP 的水平。ZEB2 的过表达逆转了 ZEB2-AS1 下调对增殖、EMT 和 Wnt/β-catenin 信号失活的影响。此外,ZEB2-AS1 敲低抑制了肿瘤生长、Ki-67 染色以及小鼠中 VEGF、MMP9、活性 β-catenin、c-Myc、cyclinD1 和 AXIN2 的表达。总之,ZEB2-AS1 促进了胃癌的肿瘤发生,这与 ZEB2 的上调和 Wnt/β-catenin 通路的激活有关。

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