Affiliation:
1. Department of Pathology, The First Affiliated Hospital of Bengbu Medical College, Changhuai Road 287#, Bengbu, Anhui 233000, China
2. Department of Emergency Internal Medicine, The Third the People′s Hospital of Bengbu, Bengbu, Anhui 233000, China
3. Department of Pathology, The Second Affiliated Hospital of Anhui Medical University, Furong Road 678#, Hefei, Anhui 233000, China
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.
Funder
Anhui Department of Education
Cited by
1 articles.
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