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Anti-angiogenic effects of testis-specific gene antigen 10 on primary endothelial cells.
Valipour, Elahe; Nooshabadi, Vajihe Taghdiri; Mahdipour, Shadi; Shabani, Sasan; Farhady-Tooli, Leila; Majidian, Sina; Noroozi, Zahra; Mansouri, Kamran; Motevaseli, Elaheh; Modarressi, Mohammad Hossein.
Afiliação
  • Valipour E; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Nooshabadi VT; Department of Tissue Engineering and Applied Cell Sciences, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
  • Mahdipour S; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Shabani S; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Farhady-Tooli L; Department of Microbiology, School of Biology, College of Science, Tehran University, Tehran, Iran.
  • Majidian S; School of Electrical Engineering, Iran University of Science and Technology, Tehran, Iran.
  • Noroozi Z; Department of Molecular Medicine, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, Iran.
  • Mansouri K; Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
  • Motevaseli E; Department of Molecular Medicine, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, Iran.
  • Modarressi MH; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: modaresi@tums.ac.ir.
Gene ; 754: 144856, 2020 Sep 05.
Article em En | MEDLINE | ID: mdl-32512160
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Movimento Celular / Neovascularização Fisiológica / Inibidores da Angiogênese / Proteínas do Citoesqueleto / Proliferação de Células / Células Endoteliais da Veia Umbilical Humana Limite: Humans Idioma: En Revista: Gene Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Movimento Celular / Neovascularização Fisiológica / Inibidores da Angiogênese / Proteínas do Citoesqueleto / Proliferação de Células / Células Endoteliais da Veia Umbilical Humana Limite: Humans Idioma: En Revista: Gene Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Irã