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生物标志物与食管鳞状细胞癌中血管生成拟态、血管内皮钙黏蛋白、Y盒转录因子17性别决定区和细胞周期蛋白D1之间的相关性

The Biomarker Like the Correlation between Vasculogenic Mimicry, Vascular Endothelial Cadherin, Sex-DeterminingRegion on Y-Box Transcription Factor 17, and Cyclin D1 in Oesophageal Squamous Cell Carcinoma.

作者信息

Qin Yanzi, Zhao Wenjun, Cai Zhaogeng, Wang Qi, Gao Jin, Ci Hongfei, Feng Zhenzhong, Ma Li

机构信息

Department of Pathology, The First Affiliated Hospital of Bengbu Medical College, Changhuai Road 287#, Bengbu, Anhui 233000, China.

Department of Emergency Internal Medicine, The Third the People's Hospital of Bengbu, Bengbu, Anhui 233000, China.

出版信息

J Oncol. 2022 Aug 29;2022:8915503. doi: 10.1155/2022/8915503. eCollection 2022.

Abstract

BACKGROUND

This study aimed to explore the relationships between the sex-determining region on Y (SRY) box transcription factor 17 (SOX17), Cyclin D1, vascular endothelial cadherin (VE-cadherin), and vasculogenic mimicry (VM) in the occurrence and development of esophageal squamous cell carcinoma (ESCC).

METHODS

The expressions of SOX17, Cyclin D1, and VE-cadherin, as well as VM, in tissues, were determined using immunohistochemistry. SOX17, Cyclin D1, and VE-cadherin mRNA in ESCC and their corresponding adjacent normal tissues were quantified using quantitative reverse transcription polymerase chain reaction analysis. Cell invasion, migration, and proliferation were determined after the silencing of VE-cadherin. SOX17, Cyclin D1, and VE-cadherin protein were quantified using Western blotting.

RESULTS

The expression levels of SOX17, Cyclin D1, and VE-cadherin significantly correlated with the clinical characteristics of ESCC. After the VE-cadherin silencing, cell invasion, migration, and proliferation decreased, along with the Cyclin D1 levels, while the SOX17 levels increased.

CONCLUSION

SOX17, Cyclin D1, and VE-cadherin are involved in the development of ESCC.

摘要

背景

本研究旨在探讨Y染色体性别决定区框转录因子17(SOX17)、细胞周期蛋白D1、血管内皮钙黏蛋白(VE-钙黏蛋白)与食管鳞状细胞癌(ESCC)发生发展过程中血管生成拟态(VM)之间的关系。

方法

采用免疫组织化学法检测组织中SOX17、细胞周期蛋白D1、VE-钙黏蛋白以及VM的表达情况。运用定量逆转录聚合酶链反应分析对ESCC及其相应癌旁正常组织中的SOX17、细胞周期蛋白D1和VE-钙黏蛋白mRNA进行定量分析。在沉默VE-钙黏蛋白后,检测细胞的侵袭、迁移和增殖情况。采用蛋白质印迹法对SOX17、细胞周期蛋白D1和VE-钙黏蛋白进行定量分析。

结果

SOX17、细胞周期蛋白D1和VE-钙黏蛋白的表达水平与ESCC的临床特征显著相关。沉默VE-钙黏蛋白后,细胞的侵袭、迁移和增殖能力下降,细胞周期蛋白D1水平降低,而SOX17水平升高。

结论

SOX17、细胞周期蛋白D1和VE-钙黏蛋白参与了ESCC的发生发展过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cce5/9444392/1e86d4332052/JO2022-8915503.001.jpg

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