Abstract |
In Taiwan, the average prevalence of congenital heart disease (CHD) is 13.08/1000 live births. Most children with CHD die before the age of 5 years; therefore, identifying treatment methods to extend the life of CHD patients is an important issue in clinical practice. The objective of this study is to evaluate the roles of hypoxia-inducible factor-1α (HIF-1α), vascular endothelial growth factor ( VEGF), inducible nitric oxide synthase (iNOS), endothelin-1 (ET-1), and CD34 in CHD autopsy cases in comparison with autopsy cases without CHD. The study included 19 autopsy cases, which were divided into the following four groups: acyanotic CHD (n = 11), cyanotic CHD (n = 3), CHD associated with chromosomal abnormalities (n = 3), and complex CHD (n = 2). Heart specimens obtained from 10 autopsy cases without CHD were included as controls. Our results indicated that high percentages of HIF-1α (100%), VEGF (89.5%), iNOS (78.9%), and ET-1 (84.2%) expressions were observed in CHD autopsy cases and this was found to be significant. HIF-1α induced by hypoxia could play a potential role in relating downstream gene expressions in CHD patients. Upregulation of VEGF by HIF-1α could play an important role in triggering angiogenesis to protect myocardial cell survival in a hypoxic microenvironment. Therefore, HIF-1α could be a significant prognosis marker in CHD and be a prospective candidate in the development of target therapy in cardiovascular diseases.
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Authors | Hsin-Ling Yin, Chi-Wen Luo, Zen-Kong Dai, Kai-Ping Shaw, Chee-Yin Chai, Chun-Chieh Wu |
Journal | The Kaohsiung journal of medical sciences
(Kaohsiung J Med Sci)
Vol. 32
Issue 7
Pg. 348-55
(Jul 2016)
ISSN: 2410-8650 [Electronic] China (Republic : 1949- ) |
PMID | 27450023
(Publication Type: Journal Article)
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Copyright | Copyright © 2016. Published by Elsevier Taiwan. |
Chemical References |
- Endothelin-1
- Hypoxia-Inducible Factor 1, alpha Subunit
- Vascular Endothelial Growth Factor A
- Nitric Oxide Synthase Type II
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Topics |
- Endothelin-1
(metabolism)
- Female
- Heart Defects, Congenital
(metabolism, pathology)
- Humans
- Hypoxia-Inducible Factor 1, alpha Subunit
(metabolism)
- Immunohistochemistry
- Infant
- Infant, Newborn
- Male
- Microvessels
(pathology)
- Neovascularization, Physiologic
- Nitric Oxide Synthase Type II
(metabolism)
- Vascular Endothelial Growth Factor A
(metabolism)
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