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Anti-Angiogenic Effects of Testis-Specific Gene Antigen 10 on Primary Endothelial Cells Publisher Pubmed



Valipour E1 ; Nooshabadi VT2 ; Mahdipour S1 ; Shabani S1 ; Farhadytooli L3 ; Majidian S4 ; Noroozi Z5 ; Mansouri K6 ; Motevaseli E5 ; Modarressi MH1
Authors
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Authors Affiliations
  1. 1. Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Tissue Engineering and Applied Cell Sciences, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran
  3. 3. Department of Microbiology, School of Biology, College of Science, Tehran University, Tehran, Iran
  4. 4. School of Electrical Engineering, Iran University of Science and Technology, Tehran, Iran
  5. 5. Department of Molecular Medicine, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran

Source: Gene Published:2020


Abstract

Growing evidence indicates the antitumor and antiangiogenesis activities of testis-specific gene antigen 10 (TSGA10). However, the underlying mechanisms and precise role of TSGA10 in angiogenesis are still elusive. In this study, we isolated human umbilical cord vein endothelial cells (HUVECs) and stably transfected with pcDNA3.1 carrying TSGA10 coding sequence. We demonstrated that TSGA10 over-expression significantly decreases HUVEC tubulogenesis and interconnected capillary network formation. HUVECs over-expressing TSGA10 exhibited a significant decrease in migration and proliferation rates. TSGA10 over-expression markedly decreased expression of angiogenesis-related genes, including VEGF-A, VEGFR-2, Ang-1, Ang-2, and Tie-2. Our ELISA results showed the decrease in VEGF-A mRNA expression level is associated with a significant decrease in its protein secretion. Additionally, over-expressing TSGA10 decreased expression levels of marker genes of cell migration (MMP-2, MMP-9, and SDF-1a) and proliferation (PCNA and Ki-67. Furthermore, ERK-1 and AKT phosphorylation significantly reduced in HUVECs over-expressing TSGA10. Our findings suggest a potent anti-angiogenesis activity of TSGA10 in HUVECs through down-regulation of ERK and AKT signalling pathways, and may provide therapeutic benefits for the management of different pathological angiogenesis. © 2020 Elsevier B.V.