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Microarray Analysis of Extracranial Arteriovenous Malformation Endothelial Cells

  • Lee, Joon Seok (Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University) ;
  • Oh, Eun Jung (Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University) ;
  • Kim, Hyun Mi (Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University) ;
  • Kwak, Suin (BK21 FOUR KNU Convergence Educational Program of Biomedical Science for Creative Future Talents, Department of Biomedical Science, School of Medicine, Kyungpook National University) ;
  • Lee, Seok-Jong (Department of Dermatology, School of Medicine, Kyungpook National University) ;
  • Lee, Jongmin (Department of Radiology, School of Medicine, Kyungpook National University) ;
  • Huh, Seung (Department of Surgery, School of Medicine, Kyungpook National University) ;
  • Kim, Ji Yoon (Department of Pediatrics, School of Medicine, Kyungpook National University) ;
  • Chung, Ho Yun (Department of Plastic and Reconstructive Surgery, School of Medicine, Kyungpook National University)
  • Received : 2022.10.01
  • Accepted : 2022.10.13
  • Published : 2022.10.31

Abstract

Background: Arteriovenous malformations (AVMs) are rare diseases comprising abnormally dilated arteries and veins with an absence of a capillary network. Since these diseases are intractable after diagnosis, various treatment strategies have been examined, with continuous efforts to identify target genes. Here, we report relevant new target genes selected via gene microarray. Methods: Endothelial cells were isolated from samples collected from three patients with AVM and three healthy individuals, followed by microarray analysis. Additionally, quantitative PCR was performed to select genes highly relevant to AVM. Results: In the vascular endothelial cells derived from the tissues of patients with AVM, the expression of ANGPT1, ANGPT2, DLL4, IL6, NRG1, TGFBR1, and VEGFA was typically higher compared to those derived from normal tissues. Conclusion: Seven candidate genes were selected to analyze the pathophysiological mechanism of AVM. These results may aid in future directions of diagnosis and treatment.

Keywords

Acknowledgement

This research was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2020R1A2C2009496).

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