Biology:Hypoxia-inducible factor

From HandWiki
Revision as of 18:36, 12 February 2024 by Sherlock (talk | contribs) (linkage)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Short description: Protein that responds to low oxygen
hypoxia-inducible factor 1, alpha subunit
Identifiers
SymbolHIF1A
NCBI gene3091
HGNC4910
OMIM603348
RefSeqNM_001530
UniProtQ16665
Other data
LocusChr. 14 q21-q24
aryl hydrocarbon receptor nuclear translocator
Identifiers
SymbolARNT
Alt. symbolsHIF1B, bHLHe2
NCBI gene405
HGNC700
OMIM126110
RefSeqNM_001668
UniProtP27540
Other data
LocusChr. 1 q21
endothelial PAS domain protein 1
Identifiers
SymbolEPAS1
Alt. symbolsHIF2A, MOP2, PASD2, HLF
NCBI gene2034
HGNC3374
OMIM603349
RefSeqNM_001430
UniProtQ99814
Other data
LocusChr. 2 p21-p16
aryl-hydrocarbon receptor nuclear translocator 2
Identifiers
SymbolARNT2
Alt. symbolsHIF2B, KIAA0307, bHLHe1
NCBI gene9915
HGNC16876
OMIM606036
RefSeqNM_014862
UniProtQ9HBZ2
Other data
LocusChr. 1 q24
hypoxia-inducible factor 3, alpha subunit
Identifiers
SymbolHIF3A
NCBI gene64344
HGNC15825
OMIM609976
RefSeqNM_152794
UniProtQ9Y2N7
Other data
LocusChr. 19 q13

Hypoxia-inducible factors (HIFs) are transcription factors that respond to decreases in available oxygen in the cellular environment, or hypoxia.[1][2] They also respond to instances of pseudohypoxia, such as thiamine deficiency.[3][4] Both hypoxia and pseudohypoxia leads to impairment of adenosine triphosphate (ATP) production by the mitochondria.

Discovery

The HIF transcriptional complex was discovered in 1995 by Gregg L. Semenza and postdoctoral fellow Guang Wang.[5][6][7] In 2016, William Kaelin Jr., Peter J. Ratcliffe and Gregg L. Semenza were presented the Lasker Award for their work in elucidating the role of HIF-1 in oxygen sensing and its role in surviving low oxygen conditions.[8] In 2019, the same three individuals were jointly awarded the Nobel Prize in Physiology or Medicine for their work in elucidating how HIF senses and adapts cellular response to oxygen availability.[9]

Structure

Oxygen-breathing species express the highly conserved transcriptional complex HIF-1, which is a heterodimer composed of an alpha and a beta subunit, the latter being a constitutively-expressed aryl hydrocarbon receptor nuclear translocator (ARNT).[6][10] HIF-1 belongs to the PER-ARNT-SIM (PAS) subfamily of the basic helix-loop-helix (bHLH) family of transcription factors. The alpha and beta subunit are similar in structure and both contain the following domains:[11][12][13]

Hypoxia-inducible factor-1
PDB 1lm8 EBI.jpg
Structure of a HIF-1a-pVHL-ElonginB-ElonginC Complex.[14]
Identifiers
SymbolHIF-1
PfamPF11413
HIF-1 alpha C terminal transactivation domain
PDB 1l3e EBI.jpg
Identifiers
SymbolHIF-1a_CTAD
PfamPF08778
InterProIPR014887
SCOP21l3e / SCOPe / SUPFAM

Members

The following are members of the human HIF family:

Member Gene Protein
HIF-1α HIF1A hypoxia-inducible factor 1, alpha subunit
HIF-1β ARNT aryl hydrocarbon receptor nuclear translocator
HIF-2α EPAS1 endothelial PAS domain protein 1
HIF-2β ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
HIF-3α HIF3A hypoxia inducible factor 3, alpha subunit
HIF-3β ARNT3 aryl-hydrocarbon receptor nuclear translocator 3

Function

HIF1α expression in haematopoietic stem cells explains the quiescence nature of stem cells[15] for being metabolically maintaining at a low rate so as to preserve the potency of stem cells for long periods in a life cycle of an organism.

The HIF signaling cascade mediates the effects of hypoxia, the state of low oxygen concentration, on the cell. Hypoxia often keeps cells from differentiating. However, hypoxia promotes the formation of blood vessels, and is important for the formation of a vascular system in embryos and tumors. The hypoxia in wounds also promotes the migration of keratinocytes and the restoration of the epithelium.[16] It is therefore not surprising that HIF-1 modulation was identified as a promising treatment paradigm in wound healing.[17]

In general, HIFs are vital to development. In mammals, deletion of the HIF-1 genes results in perinatal death.[18] HIF-1 has been shown to be vital to chondrocyte survival, allowing the cells to adapt to low-oxygen conditions within the growth plates of bones. HIF plays a central role in the regulation of human metabolism.[19]

Mechanism

Nobel Prize in Physiology or Medicine 2019: How Cells Sense and Adapt to Oxygen Availability. Under normoxic conditions, Hif-1 alpha is hydroxylated at two proline residues. It then associates with VHL and is tagged with ubiquitin resulting in proteasomal degradation. Under hypoxic conditions, Hif-1 alpha translocates to the cell nucleus and associates with Hif-1 beta. This complex then binds to the HRE region of the DNA resulting in the transcription of genes that are involved in a multitude of processes including erythropoesis, glycolysis, and angiogenesis.

The alpha subunits of HIF are hydroxylated at conserved proline residues by HIF prolyl-hydroxylases, allowing their recognition and ubiquitination by the VHL E3 ubiquitin ligase, which labels them for rapid degradation by the proteasome.[20][21] This occurs only in normoxic conditions. In hypoxic conditions, HIF prolyl-hydroxylase is inhibited, since it utilizes oxygen as a cosubstrate.[22][23]

Inhibition of electron transfer in the succinate dehydrogenase complex due to mutations in the SDHB or SDHD genes can cause a build-up of succinate that inhibits HIF prolyl-hydroxylase, stabilizing HIF-1α. This is termed pseudohypoxia.

HIF-1, when stabilized by hypoxic conditions, upregulates several genes to promote survival in low-oxygen conditions. These include glycolysis enzymes, which allow ATP synthesis in an oxygen-independent manner, and vascular endothelial growth factor (VEGF), which promotes angiogenesis. HIF-1 acts by binding to hypoxia-responsive elements (HREs) in promoters that contain the sequence 5'-RCGTG-3' (where R is a purine, either A or G). Studies demonstrate that hypoxia modulates histone methylation and reprograms chromatin.[24] This paper was published back-to-back with that of 2019 Nobel Prize in Physiology or Medicine winner for Medicine William Kaelin Jr.[25] This work was highlighted in an independent editorial.[26]

It has been shown that muscle A kinase–anchoring protein (mAKAP) organized E3 ubiquitin ligases, affecting stability and positioning of HIF-1 inside its action site in the nucleus. Depletion of mAKAP or disruption of its targeting to the perinuclear (in cardiomyocytes) region altered the stability of HIF-1 and transcriptional activation of genes associated with hypoxia. Thus, "compartmentalization" of oxygen-sensitive signaling components may influence the hypoxic response.[27]

The advanced knowledge of the molecular regulatory mechanisms of HIF1 activity under hypoxic conditions contrast sharply with the paucity of information on the mechanistic and functional aspects governing NF-κB-mediated HIF1 regulation under normoxic conditions. However, HIF-1α stabilization is also found in non-hypoxic conditions through an unknown mechanism. It was shown that NF-κB (nuclear factor κB) is a direct modulator of HIF-1α expression in the presence of normal oxygen pressure. siRNA (small interfering RNA) studies for individual NF-κB members revealed differential effects on HIF-1α mRNA levels, indicating that NF-κB can regulate basal HIF-1α expression. Finally, it was shown that, when endogenous NF-κB is induced by TNFα (tumour necrosis factor α) treatment, HIF-1α levels also change in an NF-κB-dependent manner.[28] HIF-1 and HIF-2 have different physiological roles. HIF-2 regulates erythropoietin production in adult life.[29]

Repair, regeneration and rejuvenation

In normal circumstances after injury HIF-1a is degraded by prolyl hydroxylases (PHDs). In June 2015, scientists found that the continued up-regulation of HIF-1a via PHD inhibitors regenerates lost or damaged tissue in mammals that have a repair response; and the continued down-regulation of Hif-1a results in healing with a scarring response in mammals with a previous regenerative response to the loss of tissue. The act of regulating HIF-1a can either turn off, or turn on the key process of mammalian regeneration.[30][31] One such regenerative process in which HIF1A is involved is skin healing.[32] Researchers at the Stanford University School of Medicine demonstrated that HIF1A activation was able to prevent and treat chronic wounds in diabetic and aged mice. Not only did the wounds in the mice heal more quickly, but the quality of the new skin was even better than the original.[33][34][35] Additionally the regenerative effect of HIF-1A modulation on aged skin cells was described[36][37] and a rejuvenating effect on aged facial skin was demonstrated in patients.[38] HIF modulation has also been linked to a beneficial effect on hair loss.[39] The biotech company Tomorrowlabs GmbH, founded in Vienna in 2016 by the physician Dominik Duscher and pharmacologist Dominik Thor, makes use of this mechanism.[40] Based on the patent-pending HSF ("HIF strengthening factor") active ingredient, products have been developed that are supposed to promote skin and hair regeneration.[41][42][43][44]

As a therapeutic target

Anemia

Several drugs that act as selective HIF prolyl-hydroxylase inhibitors have been developed.[45][46] The most notable compounds are: Roxadustat (FG-4592);[47] Vadadustat (AKB-6548),[48] Daprodustat (GSK1278863),[49] Desidustat (ZYAN-1),[50] and Molidustat (Bay 85-3934),[51] all of which are intended as orally acting drugs for the treatment of anemia.[52] Other significant compounds from this family, which are used in research but have not been developed for medical use in humans, include MK-8617,[53] YC-1,[54] IOX-2,[55] 2-methoxyestradiol,[56] GN-44028,[57] AKB-4924,[58] Bay 87-2243,[59] FG-2216[60] and FG-4497.[61] By inhibiting prolyl-hydroxylase enzyme, the stability of HIF-2α in the kidney is increased, which results in an increase in endogenous production of erythropoietin.[62] Both FibroGen compounds made it through to Phase II clinical trials, but these were suspended temporarily in May 2007 following the death of a trial participant taking FG-2216 from fulminant hepatitis (liver failure), however it is unclear whether this death was actually caused by FG-2216. The hold on further testing of FG-4592 was lifted in early 2008, after the FDA reviewed and approved a thorough response from FibroGen.[63] Roxadustat, vadadustat, daprodustat and molidustat have now all progressed through to Phase III clinical trials for treatment of renal anemia.[47][48][49]

Inflammation and cancer

In other scenarios and in contrast to the therapy outlined above, research suggests that HIF induction in normoxia is likely to have serious consequences in disease settings with a chronic inflammatory component.[64][65][66] It has also been shown that chronic inflammation is self-perpetuating and that it distorts the microenvironment as a result of aberrantly active transcription factors. As a consequence, alterations in growth factor, chemokine, cytokine, and ROS balance occur within the cellular milieu that in turn provide the axis of growth and survival needed for de novo development of cancer and metastasis. These results have numerous implications for a number of pathologies where NF-κB and HIF-1 are deregulated, including rheumatoid arthritis and cancer.[67][68][69][70][71][72] Therefore, it is thought that understanding the cross-talk between these two key transcription factors, NF-κB and HIF, will greatly enhance the process of drug development.[28][73]

HIF activity is involved in angiogenesis required for cancer tumor growth, so HIF inhibitors such as phenethyl isothiocyanate and Acriflavine[74] are (since 2006) under investigation for anti-cancer effects.[75][76][77]

Neurology

Research conducted on mice suggests that stabilizing HIF using an HIF prolyl-hydroxylase inhibitor enhances hippocampal memory, likely by increasing erythropoietin expression.[78] HIF pathway activators such as ML-228 may have neuroprotective effects and are of interest as potential treatments for stroke and spinal cord injury.[79][80]

von Hippel–Lindau disease-associated renal cell carcinoma

Belzutifan is an hypoxia-inducible factor-2α inhibitor[81] under investigation for the treatment of von Hippel–Lindau disease-associated renal cell carcinoma.[82][83][84][85]

References

  1. ↑ "The human side of hypoxia-inducible factor". British Journal of Haematology 141 (3): 325–34. May 2008. doi:10.1111/j.1365-2141.2008.07029.x. PMID 18410568. 
  2. ↑ "Targeting Protein-Protein Interactions in the HIF System". ChemMedChem 11 (8): 773–86. April 2016. doi:10.1002/cmdc.201600012. PMID 26997519. 
  3. ↑ Rl, Sweet; Ja, Zastre (2013). "HIF1-α-mediated gene expression induced by vitamin B1 deficiency" (in en). International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition 83 (3): 188–197. doi:10.1024/0300-9831/a000159. ISSN 0300-9831. PMID 24846908. https://pubmed.ncbi.nlm.nih.gov/24846908/. 
  4. ↑ C, Marrs; D, Lonsdale (2021-09-29). "Hiding in Plain Sight: Modern Thiamine Deficiency" (in en). Cells 10 (10): 2595. doi:10.3390/cells10102595. ISSN 2073-4409. PMID 34685573. 
  5. ↑ "Purification and characterization of hypoxia-inducible factor 1". The Journal of Biological Chemistry 270 (3): 1230–7. January 1995. doi:10.1074/jbc.270.3.1230. PMID 7836384. 
  6. ↑ 6.0 6.1 "Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension". Proceedings of the National Academy of Sciences of the United States of America 92 (12): 5510–4. June 1995. doi:10.1073/pnas.92.12.5510. PMID 7539918. Bibcode: 1995PNAS...92.5510W. 
  7. ↑ "Hypoxia and Hypoxia Inducible Factors (HIF) as Important Regulators of Tumor Physiology". Angiogenesis in Brain Tumors. Cancer Treatment and Research. 117. 2004. pp. 219–48. doi:10.1007/978-1-4419-8871-3_14. ISBN 978-1-4613-4699-9. 
  8. ↑ "Oxygen sensing – an essential process for survival". Albert Lasker Basic Medical Research Award. Albert And Mary Lasker Foundation. 2016. http://www.laskerfoundation.org/awards/show/oxygen-sensing-essential-process-survival/. 
  9. ↑ "How cells sense and adapt to oxygen availability". The Nobel Prize in Physiology or Medicine 2019. NobelPrize.org. Nobel Media AB. 7 October 2019. https://www.nobelprize.org/prizes/medicine/2019/press-release/. 
  10. ↑ "Dimerization, DNA binding, and transactivation properties of hypoxia-inducible factor 1". The Journal of Biological Chemistry 271 (30): 17771–8. July 1996. doi:10.1074/jbc.271.30.17771. PMID 8663540. 
  11. ↑ "PAS domain S-boxes in Archaea, Bacteria and sensors for oxygen and redox". Trends in Biochemical Sciences 22 (9): 331–3. September 1997. doi:10.1016/S0968-0004(97)01110-9. PMID 9301332. 
  12. ↑ "PAS: a multifunctional domain family comes to light". Current Biology 7 (11): R674-7. November 1997. doi:10.1016/S0960-9822(06)00352-6. PMID 9382818. https://ora.ox.ac.uk/objects/uuid:a355e492-0292-4db5-968d-06c4470e188f. 
  13. ↑ "Functions of the Per/ARNT/Sim domains of the hypoxia-inducible factor". The Journal of Biological Chemistry 280 (43): 36047–54. October 2005. doi:10.1074/jbc.M501755200. PMID 16129688. 
  14. ↑ "Structure of an HIF-1alpha -pVHL complex: hydroxyproline recognition in signaling". Science 296 (5574): 1886–9. June 2002. doi:10.1126/science.1073440. PMID 12004076. Bibcode: 2002Sci...296.1886M. 
  15. ↑ "Anaerobic Glycolysis and HIF1α Expression in Haematopoietic Stem Cells Explains Its Quiescence Nature". Journal of Stem Cells 10 (2): 97–106. 2015. PMID 27125138. 
  16. ↑ "The magic of the hypoxia-signaling cascade". Cellular and Molecular Life Sciences 65 (7–8): 1133–49. April 2008. doi:10.1007/s00018-008-7472-0. PMID 18202826. 
  17. ↑ "Comparison of the Hydroxylase Inhibitor Dimethyloxalylglycine and the Iron Chelator Deferoxamine in Diabetic and Aged Wound Healing". Plastic and Reconstructive Surgery 139 (3): 695e–706e. March 2017. doi:10.1097/PRS.0000000000003072. PMID 28234841. 
  18. ↑ "Fibroblast-Specific Deletion of Hypoxia Inducible Factor-1 Critically Impairs Murine Cutaneous Neovascularization and Wound Healing". Plastic and Reconstructive Surgery 136 (5): 1004–13. November 2015. doi:10.1097/PRS.0000000000001699. PMID 26505703. 
  19. ↑ "Regulation of human metabolism by hypoxia-inducible factor". Proceedings of the National Academy of Sciences of the United States of America 107 (28): 12722–7. July 2010. doi:10.1073/pnas.1002339107. PMID 20616028. Bibcode: 2010PNAS..10712722F. 
  20. ↑ "The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis". Nature 399 (6733): 271–5. May 1999. doi:10.1038/20459. PMID 10353251. Bibcode: 1999Natur.399..271M. 
  21. ↑ "Seeking a Cellular Oxygen Sensor". The Scientist. May 2001. https://www.the-scientist.com/research/seeking-a-cellular-oxygen-sensor-54701. 
  22. ↑ "Hydroxylation of HIF-1: oxygen sensing at the molecular level". Physiology 19 (4): 176–82. August 2004. doi:10.1152/physiol.00001.2004. PMID 15304631. 
  23. ↑ "Discovering HIF Regulation". The Scientist. April 2003. https://www.the-scientist.com/hot-paper/discovering-hif-regulation-51758. 
  24. ↑ "Hypoxia induces rapid changes to histone methylation and reprograms chromatin". Science 363 (6432): 1222–1226. March 2019. doi:10.1126/science.aau5870. PMID 30872526. Bibcode: 2019Sci...363.1222B. 
  25. ↑ "Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate". Science 363 (6432): 1217–1222. March 2019. doi:10.1126/science.aaw1026. PMID 30872525. PMC 7336390. Bibcode: 2019Sci...363.1217C. http://urn.fi/urn:nbn:fi-fe201903259863. 
  26. ↑ "Histone modifiers are oxygen sensors". Science 363 (6432): 1148–1149. March 2019. doi:10.1126/science.aaw8373. PMID 30872506. Bibcode: 2019Sci...363.1148G. https://www.repository.cam.ac.uk/handle/1810/291099. 
  27. ↑ "mAKAP compartmentalizes oxygen-dependent control of HIF-1alpha". Science Signaling 1 (51): ra18. December 2008. doi:10.1126/scisignal.2000026. PMID 19109240. 
  28. ↑ 28.0 28.1 "Regulation of hypoxia-inducible factor-1alpha by NF-kappaB". The Biochemical Journal 412 (3): 477–84. June 2008. doi:10.1042/BJ20080476. PMID 18393939. 
  29. ↑ "Hypoxic regulation of erythropoiesis and iron metabolism". American Journal of Physiology. Renal Physiology 299 (1): F1-13. July 2010. doi:10.1152/ajprenal.00174.2010. PMID 20444740. 
  30. ↑ eurekalert.org staff (3 June 2015). "Scientist at LIMR leads study demonstrating drug-induced tissue regeneration". Lankenau Institute for Medical Research (LIMR). http://www.eurekalert.org/pub_releases/2015-06/mlhl-sal060215.php. 
  31. ↑ "Drug-induced regeneration in adult mice". Science Translational Medicine 7 (290): 290ra92. June 2015. doi:10.1126/scitranslmed.3010228. PMID 26041709. 
  32. ↑ "The Role of Hypoxia-Inducible Factor in Wound Healing". Advances in Wound Care 3 (5): 390–399. May 2014. doi:10.1089/wound.2013.0520. PMID 24804159. 
  33. ↑ "Transdermal deferoxamine prevents pressure-induced diabetic ulcers". Proceedings of the National Academy of Sciences of the United States of America 112 (1): 94–9. January 2015. doi:10.1073/pnas.1413445112. PMID 25535360. Bibcode: 2015PNAS..112...94D. 
  34. ↑ "Optimization of transdermal deferoxamine leads to enhanced efficacy in healing skin wounds". Journal of Controlled Release 308: 232–239. August 2019. doi:10.1016/j.jconrel.2019.07.009. PMID 31299261. 
  35. ↑ "Deferoxamine can prevent pressure ulcers and accelerate healing in aged mice". Wound Repair and Regeneration 26 (3): 300–305. May 2018. doi:10.1111/wrr.12667. PMID 30152571. 
  36. ↑ "duscher hif - Search Results - PubMed" (in en). https://pubmed.ncbi.nlm.nih.gov/?term=duscher%20hif. 
  37. ↑ "Deferiprone Stimulates Aged Dermal Fibroblasts Via HIF-1α Modulation". Aesthetic Surgery Journal 41 (4): 514–524. June 2020. doi:10.1093/asj/sjaa142. PMID 32479616. 
  38. ↑ "A single-center blinded randomized clinical trial to evaluate the anti-aging effects of a novel HSF™-based skin care formulation". Journal of Cosmetic Dermatology 19 (11): 2936–2945. November 2020. doi:10.1111/jocd.13356. PMID 32306525. 
  39. ↑ "Molecular Mechanisms of Hair Growth and Regeneration: Current Understanding and Novel Paradigms". Dermatology 236 (4): 271–280. 2020. doi:10.1159/000506155. PMID 32163945. 
  40. ↑ Tomorrowlabs. "Tomorrowlabs" (in en). https://www.tomorrowlabs.at/. 
  41. ↑ "Kosmetikbranche: Wie das Beauty-Start-up Tomorrowlabs den Markt erobert" (in de). https://www.handelsblatt.com/unternehmen/mittelstand/familienunternehmer/kosmetikbranche-wie-das-beauty-start-up-tomorrowlabs-den-markt-erobert/25523424.html. 
  42. ↑ "Das neue Beauty-Investment von Michael Pieper - HZ" (in de). https://www.handelszeitung.ch/unternehmen/das-neue-beauty-investment-von-michael-pieper. 
  43. ↑ andrea.hodoschek (2020-08-03). "Milliardenmarkt Anti-Aging: Start-up aus Österreich mischt mit" (in de). https://kurier.at/wirtschaft/wirtschaft-von-innen/milliardenmarkt-anti-aging-start-up-aus-oesterreich-mischt-mit/400989071. 
  44. ↑ "Ein Protein gegen das Altern und für das Geldverdienen" (in de). https://www.nachrichten.at/wirtschaft/wirtschaftsraumooe/ein-protein-gegen-das-altern-und-fuer-das-geldverdienen;art467,3277897. 
  45. ↑ "Hydroxylation of hypoxia-inducible transcription factors and chemical compounds targeting the HIF-alpha hydroxylases". Current Medicinal Chemistry 14 (17): 1853–62. 2007. doi:10.2174/092986707781058850. PMID 17627521. 
  46. ↑ "HIF prolyl hydroxylase inhibitors for the treatment of renal anaemia and beyond". Nature Reviews. Nephrology 12 (3): 157–68. March 2016. doi:10.1038/nrneph.2015.193. PMID 26656456. https://www.repository.cam.ac.uk/handle/1810/253687. 
  47. ↑ 47.0 47.1 "A New Approach to the Management of Anemia in CKD Patients: A Review on Roxadustat". Advances in Therapy 34 (4): 848–853. April 2017. doi:10.1007/s12325-017-0508-9. PMID 28290095. 
  48. ↑ 48.0 48.1 "Vadadustat, a novel oral HIF stabilizer, provides effective anemia treatment in nondialysis-dependent chronic kidney disease". Kidney International 90 (5): 1115–1122. November 2016. doi:10.1016/j.kint.2016.07.019. PMID 27650732. 
  49. ↑ 49.0 49.1 "Discovery and Preclinical Characterization of GSK1278863 (Daprodustat), a Small Molecule Hypoxia Inducible Factor-Prolyl Hydroxylase Inhibitor for Anemia". The Journal of Pharmacology and Experimental Therapeutics 363 (3): 336–347. December 2017. doi:10.1124/jpet.117.242503. PMID 28928122. 
  50. ↑ "Phase I Clinical Study of ZYAN1, A Novel Prolyl-Hydroxylase (PHD) Inhibitor to Evaluate the Safety, Tolerability, and Pharmacokinetics Following Oral Administration in Healthy Volunteers". Clinical Pharmacokinetics 57 (1): 87–102. January 2018. doi:10.1007/s40262-017-0551-3. PMID 28508936. 
  51. ↑ "Mimicking hypoxia to treat anemia: HIF-stabilizer BAY 85-3934 (Molidustat) stimulates erythropoietin production without hypertensive effects". PLOS ONE 9 (11): e111838. 2014. doi:10.1371/journal.pone.0111838. PMID 25392999. Bibcode: 2014PLoSO...9k1838F. 
  52. ↑ "The latest advances in kidney diseases and related disorders". Drug News & Perspectives 20 (10): 647–54. December 2007. PMID 18301799. http://journals.prous.com/journals/servlet/xmlxsl/pk_journals.xml_summaryn_pr?p_JournalId=3&p_RefId=3919. 
  53. ↑ "Discovery of N-[Bis(4-methoxyphenyl)methyl]-4-hydroxy-2-(pyridazin-3-yl)pyrimidine-5-carboxamide (MK-8617), an Orally Active Pan-Inhibitor of Hypoxia-Inducible Factor Prolyl Hydroxylase 1-3 (HIF PHD1-3) for the Treatment of Anemia". Journal of Medicinal Chemistry 59 (24): 11039–11049. December 2016. doi:10.1021/acs.jmedchem.6b01242. PMID 28002958. 
  54. ↑ "YC-1: a potential anticancer drug targeting hypoxia-inducible factor 1". Journal of the National Cancer Institute 95 (7): 516–25. April 2003. doi:10.1093/jnci/95.7.516. PMID 12671019. 
  55. ↑ "Impairment of hypoxia-induced HIF-1α signaling in keratinocytes and fibroblasts by sulfur mustard is counteracted by a selective PHD-2 inhibitor". Archives of Toxicology 90 (5): 1141–50. May 2016. doi:10.1007/s00204-015-1549-y. PMID 26082309. 
  56. ↑ "Cancer therapeutic agents targeting hypoxia-inducible factor-1". Current Medicinal Chemistry 18 (21): 3168–89. 2011. doi:10.2174/092986711796391606. PMID 21671859. 
  57. ↑ "Discovery of Indenopyrazoles as a New Class of Hypoxia Inducible Factor (HIF)-1 Inhibitors". ACS Medicinal Chemistry Letters 4 (2): 297–301. February 2013. doi:10.1021/ml3004632. PMID 24900662. 
  58. ↑ "A new pharmacological agent (AKB-4924) stabilizes hypoxia inducible factor-1 (HIF-1) and increases skin innate defenses against bacterial infection". Journal of Molecular Medicine 90 (9): 1079–89. September 2012. doi:10.1007/s00109-012-0882-3. PMID 22371073. 
  59. ↑ "Hypoxia-Dependent HIF-1 Activation Impacts on Tissue Remodeling in Graves' Ophthalmopathy-Implications for Smoking". The Journal of Clinical Endocrinology and Metabolism 101 (12): 4834–4842. December 2016. doi:10.1210/jc.2016-1279. PMID 27610652. 
  60. ↑ "Hypoxia-inducible factor stabilizers and other small-molecule erythropoiesis-stimulating agents in current and preventive doping analysis". Drug Testing and Analysis 4 (11): 830–45. November 2012. doi:10.1002/dta.390. PMID 22362605. 
  61. ↑ "FG-4497: a new target for acute respiratory distress syndrome?". Expert Review of Respiratory Medicine 9 (4): 405–9. August 2015. doi:10.1586/17476348.2015.1065181. PMID 26181437. 
  62. ↑ "HIF prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaques". Blood 110 (6): 2140–7. September 2007. doi:10.1182/blood-2007-02-073254. PMID 17557894. 
  63. ↑ "The FDA Accepts the Complete Response for Clinical Holds of FG-2216/FG-4592 for the Treatment of Anemia". http://www.astellas.com/en/corporate/news/pdf/080402_eg.pdf. 
  64. ↑ "Targeting hypoxia signalling for the treatment of ischaemic and inflammatory diseases". Nature Reviews. Drug Discovery 13 (11): 852–69. November 2014. doi:10.1038/nrd4422. PMID 25359381. 
  65. ↑ "AMPK and HIF signaling pathways regulate both longevity and cancer growth: the good news and the bad news about survival mechanisms". Biogerontology 17 (4): 655–80. August 2016. doi:10.1007/s10522-016-9655-7. PMID 27259535. 
  66. ↑ "Hypoxia-dependent regulation of inflammatory pathways in immune cells". The Journal of Clinical Investigation 126 (10): 3716–3724. October 2016. doi:10.1172/JCI84433. PMID 27454299. 
  67. ↑ "The role of HIF in immunity and inflammation". Molecular Aspects of Medicine 47-48: 24–34. 2016. doi:10.1016/j.mam.2015.12.004. PMID 26768963. 
  68. ↑ "Hypoxia-Inducible Factor (HIF) as a Target for Novel Therapies in Rheumatoid Arthritis". Frontiers in Pharmacology 7: 184. 2016. doi:10.3389/fphar.2016.00184. PMID 27445820. 
  69. ↑ "Clinical importance of FASN in relation to HIF-1α and SREBP-1c in gastric adenocarcinoma". Life Sciences 224: 169–176. May 2019. doi:10.1016/j.lfs.2019.03.056. PMID 30914315. https://www.sciencedirect.com/science/article/abs/pii/S0024320519302206. 
  70. ↑ "Overexpression of hypoxia-inducible factor and metabolic pathways: possible targets of cancer". Cell & Bioscience 7: 62. 2017. doi:10.1186/s13578-017-0190-2. PMID 29158891. 
  71. ↑ "Hypoxia inducible factor (HIF) in the tumor microenvironment: friend or foe?". Science China Life Sciences 60 (10): 1114–1124. October 2017. doi:10.1007/s11427-017-9178-y. PMID 29039125. 
  72. ↑ "Downregulation of fatty acid oxidation by involvement of HIF-1α and PPARγ in human gastric adenocarcinoma and its related clinical significance". Journal of Physiology and Biochemistry 77 (2): 249–260. May 2021. doi:10.1007/s13105-021-00791-3. PMID 33730333. https://pubmed.ncbi.nlm.nih.gov/33730333/. 
  73. ↑ "NF-κB and HIF crosstalk in immune responses". The FEBS Journal 283 (3): 413–24. February 2016. doi:10.1111/febs.13578. PMID 26513405. 
  74. ↑ "Acriflavine inhibits HIF-1 dimerization, tumor growth, and vascularization". Proceedings of the National Academy of Sciences of the United States of America 106 (42): 17910–5. October 2009. doi:10.1073/pnas.0909353106. PMID 19805192. Bibcode: 2009PNAS..10617910L. 
  75. ↑ "In vivo modulation of 4E binding protein 1 (4E-BP1) phosphorylation by watercress: a pilot study". The British Journal of Nutrition 104 (9): 1288–96. November 2010. doi:10.1017/S0007114510002217. PMID 20546646. 
  76. ↑ "Evaluation of HIF-1 inhibitors as anticancer agents". Drug Discovery Today 12 (19–20): 853–9. October 2007. doi:10.1016/j.drudis.2007.08.006. PMID 17933687. 
  77. ↑ "Inhibiting hypoxia-inducible factor 1 for cancer therapy". Molecular Cancer Research 4 (9): 601–5. September 2006. doi:10.1158/1541-7786.MCR-06-0235. PMID 16940159. 
  78. ↑ "Hypoxia inducible factor stabilization leads to lasting improvement of hippocampal memory in healthy mice". Behavioural Brain Research 208 (1): 80–4. March 2010. doi:10.1016/j.bbr.2009.11.010. PMID 19900484. 
  79. ↑ "HIF-1α Activation Attenuates IL-6 and TNF-α Pathways in Hippocampus of Rats Following Transient Global Ischemia". Cellular Physiology and Biochemistry 39 (2): 511–20. 2016. doi:10.1159/000445643. PMID 27383646. 
  80. ↑ "Effect of hypoxia-inducible factor-1/vascular endothelial growth factor signaling pathway on spinal cord injury in rats". Experimental and Therapeutic Medicine 13 (3): 861–866. March 2017. doi:10.3892/etm.2017.4049. PMID 28450910. 
  81. ↑ "Inhibition of hypoxia-inducible factor-2α in renal cell carcinoma with belzutifan: a phase 1 trial and biomarker analysis". Nat Med 27 (5): 802–805. April 2021. doi:10.1038/s41591-021-01324-7. PMID 33888901. 
  82. ↑ "Belzutifan". 18 March 2021. https://www.sps.nhs.uk/medicines/belzutifan/. 
  83. ↑ "MHRA awards first 'innovation passport' under new pathway". RAPS (Press release). Retrieved 25 April 2021.
  84. ↑ "Merck Receives Priority Review From FDA for New Drug Application for HIF-2α Inhibitor Belzutifan (MK-6482)" (Press release). Merck. 16 March 2016. Retrieved 25 April 2021 – via Business Wire.
  85. ↑ "FDA Grants Priority Review to Belzutifan for von Hippel-Lindau Disease–Associated RCC". 16 March 2021. https://www.cancernetwork.com/view/fda-grants-priority-review-to-belzutifan-for-von-hippel-lindau-disease-associated-rcc. 

External links

  • Hypoxia-Inducible+Factor+1 at the US National Library of Medicine Medical Subject Headings (MeSH)
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Hypoxia-inducible factor 1-alpha
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Aryl hydrocarbon receptor nuclear translocator
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Endothelial PAS domain-containing protein 1
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Hypoxia-inducible factor 3-alpha
  • short scientific animation visualises the crystal structure of the Heterodimeric HIF-1a:ARNT Complex with HRE DNA



Retrieved from "https://handwiki.org/wiki/index.php?title=Biology:Hypoxia-inducible_factor&oldid=3613538"