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Global Expression Profiling Identifies a Novel Hyaluronan Synthases 2 Gene in the Pathogenesis of Lower Extremity Varicose Veins.
Hsieh, Chia-Shan; Tsai, Chia-Ti; Chen, Yau-Hung; Chang, Sheng-Nan; Hwang, Juey-Jen; Chuang, Eric Y; Wu, I-Hui.
Afiliação
  • Hsieh CS; Department of Life Science, Genome and Systems Biology Degree Program, National Taiwan University, Taipei 10617, Taiwan. cometrise@gmail.com.
  • Tsai CT; Bioinformatics and Biostatistics Core, Center of Genomic Medicine, National Taiwan University, Taipei 10055, Taiwan. cometrise@gmail.com.
  • Chen YH; Division of Cardiology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10002, Taiwan. cttsai1999@gmail.com.
  • Chang SN; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei 10051, Taiwan. cttsai1999@gmail.com.
  • Hwang JJ; Department of Chemistry, Tamkang University, Taipei 25137, Taiwan. yauhung@mail.tku.edu.tw.
  • Chuang EY; Department of Internal Medicine, National Taiwan University Hospital Yun-Lin Branch, Yun-Lin 64041, Taiwan. p95421008@ntu.edu.tw.
  • Wu IH; Division of Cardiology, Department of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei 10002, Taiwan. jueyhwang@ntu.edu.tw.
J Clin Med ; 7(12)2018 Dec 11.
Article em En | MEDLINE | ID: mdl-30544995
Lower extremities varicose veins (VV) are among the most easily recognized venous abnormalities. The genetic mechanism of VV is largely unknown. In this study, we sought to explore the global expressional change of VV and identify novel genes that might play a role in VV. We used next-generation ribonucleic acid (RNA) sequence (RNA seq) technology to study the global messenger RNA expressional change in the venous samples of five diseased and five control patients. We identified several differentially expressed genes, which were further confirmed by conventional reverse transcription polymerase chain reaction (RT-PCR). Using these significant genes we performed in silico pathway analyses and found distinct transcriptional networks, such as angiogenesis, cell adhesion, vascular injury, and carbohydrate metabolisms that might be involved in the mechanism of VV. Among these significant genes, we also found hyaluronan synthases 2 gene (HAS2) played a pivotal role and governed all these pathways. We further confirmed that HAS2 expression was decreased in the venous samples of patients with VV. Finally, we used a zebrafish model with fluorescence emitting vasculature and red blood cells to see the morphological changes of the venous system and blood flow. We found that HAS2 knockdown in zebrafish resulted in dilated venous structural with static venous flow. HAS2 may modulate the transcriptional networks of angiogenesis, cell adhesion, vascular injury, and carbohydrate metabolisms in venous tissues and downregulation of HAS2 may underlie the mechanism of VV.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: J Clin Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: J Clin Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Suíça