Hypoxia inducing factor related genetic adaptation in high-altitude and pharmacological modulation
10.16438/j.0513-4870.2019-0010
- VernacularTitle:高原适应遗传学缺氧诱导因子通路相关基因及其药理学研究进展
- Author:
Qi-lian HE
1
,
2
,
3
;
Ri-li GE
1
,
2
;
Zhan-qiang LI
1
,
2
;
Dian-xiang LU
1
,
2
Author Information
1. Research Center for High Altitude Medicine
2. Key Laboratory of Application and Foundation for High Altitude, Medicine Research in Qinghai Province, Qinghai-Utah Joint Research key Laboratory for High Altitude Medicine
3. Medical Department, Medical College, Qinghai University, Xining 810001, China
- Publication Type:Research Article
- Keywords:
hypoxia;
altitude;
adaptation;
hypoxia-inducible factor;
prolyl hydroxylases domain
- From:
Acta Pharmaceutica Sinica
2019;54(4):611-619
- CountryChina
- Language:Chinese
-
Abstract:
Adaptation to hypoxia of the plateau environment has been a focus of scientific research in decades. The geographical distributions of such living environment include the Qinghai-Tibet Plateau, Andean Plateau in South America and Ethiopian Plateau. Over the past century, the unique features of physiological adaptation to high-altitude chronic hypoxia have been documented scientifically. The genetic studies of hypoxic adaptation in the past decade have revealed genetic bases of human high-altitude adaptation, with a close relationship to the hypoxia inducible factor (HIF) pathway and hypoxia response elements (HREs). Interestingly, the genetic pattern of adaptation to hypoxia is not the same among the three plateau populations. Tibetan has developed the best high-altitude adaptation, with modification of the HIF pathway as the key genetic element. Due to the wide range of HIF pathways, HIFs could regulate hundreds of downstream genes and are closely related to various diseases such as cancer, inflammation, ischemia, acute organ damage and infection, etc. The treatment researches of these diseases through HIFs-related regulations have led to the development of stabilizers and inhibitors of HIF pathway. We review here the adaptive responses of the three plateau populations to the hypoxic environment, and the genetic mechanism of HIF and HREs in the different ethnic high-altitude populations. Classes of HIF inhibitors, such as PI3K and/or mammalian target of rapamycin (mTOR) inhibitors, DNA-binding inhibitors, histone deacetylase inhibitors, heat-shock protein 90 inhibitors, cardiac glycosides, transcription inhibitors, topoisomerase inhibitors, and HIF activators including 2-OG mimics, Fe2+ chelators, prolyl hydroxylase (PHD) active-site blockers and CUL2 deneddylators have been presented with the drug examples. In addition, the top 3 chemical-disease and chemical-gene (protein) co-occurrences have been presented from the Pubmed literature search. The review could serve as references for research of hypoxia adaptation and HIF-related diseases.
