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Hypoxia-inducible factor-1: Physiological and Pathological Response to Hypoxia of Cell

Yıl 2014, , 171 - 177, 01.12.2014
https://doi.org/10.5505/sakaryamj.2014.15010

Öz

Hypoxia-inducible factor 1 (HIF-1) which has a critical role in the homeostasis of oxygen, is a transcriptional regulator of metabolic processes such as angiogenesis, erythropoiesis, iron metabolism and glucose metabolism. It is also essential for the regulation of key physiological systems in the process of fetal and postnatal life. HIF-1 is a heterodimeric protein consists of HIF-1α (homologues HIF-2α and HIF-2α) that involved in the regulation of oxygen and HIF-1β subunits that situated in the nucleus. Stability and activity of HIF-1α subunit is provided with post-transcriptional modification such as hydroxylation, ubiquitination, acetylation and phosphorylation. In normoxia, this regulation that starting with two proline hydroxylation and lysine acetylation which are located in region HIF-1α oxygen-dependent degradation (ODD), is carried out with a tumor suppressor gene von Hippel-Lindau protein (pVHL) and E3 ligase complex by the ubiquitin-proteasome pathway. In hypoxic conditions, HIF-1α subunits that are not hydroxylation becomes stable and switches nucleus by activating with coactivators such as cAMP, protein/p300. Combining with HIF-1β subunit regulates the expression of genes in response to hypoxia. Overexpression of HIF-1 is determined in various cancer events and targeting HIF-1 is thought to be new approach in cancer treatment.

Kaynakça

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Hipoksiyle İndüklenen Faktör-1: Hücrenin Hipoksiye Fizyolojik ve Patolojik Cevabı

Yıl 2014, , 171 - 177, 01.12.2014
https://doi.org/10.5505/sakaryamj.2014.15010

Öz

Oksijen homeostazında kritik bir rol oynayan hipoksiyle indüklenen faktör-1 (HIF-1); anjiyogenezis, eritropoezis, demir metabolizması ve glukoz metabolizması gibi metabolik süreçlerin transkripsiyonel regülatörüdür. Ayrıca fetal ve posnatal hayat sürecinde anahtar fizyolojik sistemlerin düzenlenmesi için gereklidir. HIF-1 heterodimerik bir protein olup oksijen regülasyonunda rol alan HIF-1α (homologları HIF-2α ve HIF-3α) ve nükleusta bulunan HIF-1β alt ünitelerinden oluşmaktadır. HIF-1'in α alt ünitesinin stabilitesi ve aktivitesi hidroksilasyon, ubikütinasyon, asetilasyon ve fosforilasyon gibi transkripsiyon sonrası modifikasyonlarla sağlanmaktadır. Normokside, HIF1-α'nın oksijen-bağımlı degradasyon (ODD) bölgesinde yer alan iki prolinin hidroksilasyonu ve bir lizinin asetilasyonuyla başlayan bu regülasyon bir tümör baskılayıcı gen olan von Hippel-Lindau proteini (pVHL) ile E3 ligaz kompleksi tarafından ubikütin-proteazom yolu ile gerçekleştirilmektedir. Hipoksik koşullarda, hidroksillenemeyen HIF-1α alt ünitesi stabil hale gelir ve cAMP, protein/p300 gibi koaktivatörler ile etkinleşerek nükleusa geçer. HIF-1β alt ünitesi ile birleşerek hipoksiye cevap genlerinin ekspresyonunu regüle eder. HIF-1'in aşırı ekspresyonu çeşitli kanser olgularında saptanmış ve HIF-1'in hedeflenmesinin kanser tedavisinde yeni bir yaklaşım olabileceği düşünülmüştür.

Kaynakça

  • Avni R, Cohen B, Neeman M. Hypoxic stres and cancer: Imaging the axis of evilin tumor metastasis. NMR Biomed 2011; 24: 569-581.
  • Bahadori B, Uitz E, Mayer A, Harauer J, Dam K, Truschnig-Wilders M, Pilger E, Renner W. Polymorphisms of the hypoxia-inducible factor 1 gene peripheral artery disease. Vascular Medicine 2010; 15(5): 371-374.
  • Berra E, Benizri E, Ginouves A, Volmat V, Roux D, Pouyssegur J. HIF prolyl- hydroxylase 2 is the key oxygen sensor setting low steady-state levels of HIF-1α in normoxia. EMBO J 2003; 22: 4082-4090.
  • Bruick RK, McKnight SL. A conserved family of prolyl-4-hydroxylases that modify HIF. Science 2001; 294: 1337-1340.
  • Brusselmans K, Bono F, Maxwell P, Dor Y, Dewerchin M, Collen D, Herbert JM, Carmeliet P. Hypoxia-inducible factor 2-α (HIF-2α) is involved in the apoptotic response to hypoglycemia but not to hypoxia. J Biol Chem 2001; 276: 39192-39196.
  • Chen C, Pore N, Behrooz A, Ismail-Beigi F, Maity A. Regulation of glut1 mRNA by hypoxia-inducible factor-1. Interaction between H-ras and hypoxia. J Biol Chem 2001; 276: 9519-9525.
  • Conway EM, Collen D, Carmeliet P. Molecular mechanisms of blood vessel growth. Cardiovasc Res 2001; 49: 507-521.
  • Dang CV, Semenza GL. Oncogenic alterations of metabolism. Trends Biochem Sci 1999; 24: 68–72.
  • Domene C, Illingworth CJR. Effects of point mutations in pVHL on the binding of HIF-1α. Proteins 2012; 80: 733-746.
  • Epstein AC, Gleadle JM, McNeill LA, Hewitson KS, O’Rourke J, Mole DR, Mukherji M, Metzen E, Wilson MI, Dhanda A, Tian YM, Masson N, Hamilton DL, Jaakola P, Barstead R, Hodgkin PH, Pugh CW, Schofield CJ, Ratcliffe PJ. C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell 2001; 107: 43-54.
  • Feldser D, Agani F, Iyer NV, Pak B, Ferreira G, Semenza GL. Reciprocal positive regulation of hypoxia-inducible factor 1alpha and insulin-like growth factor 2. Cancer Res 1999; 59: 3915-3918.
  • Gorlach A, Diebold I, Schini-Kerth VB, Berchner-Pfannschmidt U, Roth U, Brandes RP, Kietzmann T, Busse R. Thrombin activates the hypoxia- inducible factor-1 signaling pathway in vascular smooth muscle cells: Role of the p22(phox)-containing NADPH oxidase. Circ Res 2001; 89: 47-54.
  • Harris AL. Hypoxia-a key regulatory factor in tumour growth. Nat Rev Cancer 2002; 2: 38-47.
  • Hes FJ, Höppener WM, Luijt RB, Lips CJM. Von Hippel-Lindau Disease. Hereditary Cancer Clinical Practice 2005; 3(4): 171-178.
  • Hon WC, Wilson MI, Harlos K, Claridge TD, Schofield CJ, Pugh CW, Maxwell PH, Ratcliffe PJ, Stuart DI, Jones EY. Structural basis for the recognition of hydroxyproline in HIF-1 by pVHL. Nature 2002; 417: 975-978.
  • Hsiao PC, Chen MK, Su SC, Ueng KC, Chen YC, Hsieh YH, Liu YF, Tsai HT, Yang SY. Hypoxia inducible factor-1a gene polymorphism G1790A and its interaction with tobacco and alcohol consumptions increase susceptibility to hepatocellular carcinoma. Journal of Surgical Onc 2010; 102: 163-169.
  • Hupp TR, Hayward RL, Vojtesek B. Strategies for p53 reactivation in human sarcoma. Cancer Cell 2012; 22(3): 283-5.
  • Iliopoulos O, Levy AP, Jiang C, Kaelin WG, Goldberg MA. Negative regulation of hypoxia-inducible genes by the von Hippel-Lindau protein. Proc Natl Acad Sci U S A 1996; 93(20): 10595-9.
  • Illingworth CJR, Loenarz C, Schofield CJ, Domene C. Chemical basis for the selectivity of the von Hippel Lindau tumor suppressor pVHL for prolyl- hydroxylated HIF-1alpha. Biochemistry 2010; 49: 6936-6944.
  • Ivan M, Kondo K, Yang H, Kim W, Valiando J, Ohh M, Salic A, Asara JM, Lane WS, Kaelin WG. HIFα targeted for VHL-mediated destruction by proline hydroxylation: implications for O2 sensing. Science 2001; 292: 464-468.
  • Jaakkola P, Mole DR, Tian YM, Wilson MI, Gielbert J, Gaskell SJ, von Kriegsheim A, Hebestreit HF, Mukherji M, Schofield CJ, Maxwell PH, Pugh CW, Ratcliffe PJ. Targeting of HIF-α to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science 2001; 292: 468- 472.
  • Jain S, Maltepe E, Lu MM, Simon C, Bradfield CA. Expression of ARNT, ARNT2, HIF1α , HIF2α and Ah receptor mRNAs in the developing mouse. Mech Dev 1998; 73: 117-123.
  • Jeong JW, Bae MK, Ahn MY, Kim SH, Sohn TK, Bae MH, Yoo MA, Song EJ, Lee KJ, Kim KW. Regulation and destabilization of HIF-1alpha by ARD1- mediated acetylation. Cell 2002; 111: 709-720.
  • Jiang BH, Agani F, Passaniti A, Semenza GL. V-SRC induces expression of hypoxia-inducible factor 1 (HIF-1) and transcription of genes encoding vascular endothelial growth factor and enolase 1: Involvement of HIF-1 in tumor progression. Cancer Res 1997; 57: 5328-5335.
  • Josko J, Gwozdz B, Jedrzejowska-Szypulka H, Hendryk S. Vascular endothelial growth factor (VEGF) and its effect on angiogenesis. Med Sci Monit 2000; 6: 1047-1052.
  • Kaelin W. The von Hippel-Lindau protein, HIF hydroxylation, and oxygen sensing. Biochem Biophys Res Commun 2005; 338(1): 627-38.
  • Kamura T, Sato S, Iwai K, Czyzyk-Krzeska M, Conaway RC, Conaway JW. Activation of HIF 1alpha ubiquitination by a reconstituted von Hippel- Lindau (VHL) tumor suppressor complex. Proc Natl Acad Sci USA. 2000; 97: 10430-10435.
  • Kanno H, Saljooque F, Yamamoto I, Hattori S, Yao M, Shuin T. Role of the von Hippel-Lindau tumor suppressor protein during neuronal differentiation. Cancer Res 2000; 60: 2820-2924.
  • Ke Q, Costa M. Hypoxia-Inducible Factor-1 (HIF-1). Mol Pharmacol 2006; 70: 1469-1480.
  • Kelsey JL. Breast cancer epidemiology: Summary and future direction. Epidemiol Rev 1993; 15: 256-263.
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  • Knechtel G, Szkandera J, Stotz M, Hofmann G, Langsenlehner U, Kripp P, Samonigg H, Renner W, Langner C, Dehchamani D, Gerger A. Single nucleotide polymorphisms in the Hypoxia-Inducible Factor-1 gene and colorectal cancer risk. Molecular Carcinogenesis 2010; 49: 805-809.
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  • Manohar SM, Padgaonkar AA, Jalota-Badhwar A, Sonawane V, Rathos MJ, Kumar S, Joshi KS. A novel inhibitor of hypoxia-inducible factor-1a P3155 also modulates PI3K pathway and inhibits growth of prostate cancer cells. BMC Cancer 2011; 11: 338-348.
  • Masson N, Willam C, Maxwell PH, Pugh CW, Ratcliffe PJ. Independent function of two destruction domains in hypoxia-inducible factor-alpha chains activated by prolyl hydroxylation. EMBO J 2001; 20: 5197-206.
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  • Maynard MA, Qi H, Chung J, Lee EHL, Kondo Y, Hara S, Conaway RC. Conaway JW, Ohh M. Multiple splice variants of the human HIF-3α locus are targets of the von Hippel-Lindau E3 Ubiquitin Ligase complex. J Biol Chem 2003; 278: 11032-11040.
  • Min JH, Yang H, Ivan M, Gertler F, Kaelin WG, Pavletich NP. Structure of an HIF-1alpha -pVHL complex: hydroxyproline recognition in signaling. Science 2002; 296: 1886-1889.
  • Minet E, Michel G, Mottet D, Raes M, Michiels C. Transduction pathways involved in Hypoxia-Inducible Factor-1 phosphorylation and activation. Free Radic Biol Med 2001; 31: 847-855.
  • Ohh M, Park CW, Ivan M, Hoffman MA, Kim T, Huang LE, Pavletich N, Chau V, Kaelin WG. Ubiquitination of hypoxia-inducible factor requires direct binding to the α-domain of the von Hippel-Lindau protein. Nat Cell Biol 2000; 2: 423-427.
  • Park S, Dadak AM, Haase V, Fontana L, Giaccia AJ, Johnson R. Hypoxia- induced gene expression occurs solely through the action of hypoxia- inducible factor 1α (HIF-1α): role of cytoplasmic trapping of HIF-2α. Mol Cell Biol 2003; 23: 4959-4971.
  • Prior SJ, Hagberg JM, Phares DA, Brown MD, Fairfull L, Ferrell RE, Roth SM. Sequence variation in hypoxia-inducible factor 1alpha (HIF1A): Association with maximal oxygen consumption. Physiol Genomics. 2003; 15(1): 20-6.
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  • Ravi R, Mookerjee B, Bhujwalla ZM, Sutter CH, Artemov D, Zeng Q, Dillehay LE, Madan A, Semenza GL, Bedi A. Regulation of tumor angiogenesis by p53-induced degradation of hypoxia-inducible factor 1alpha. Genes Dev 2000; 14: 34-44.
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  • Semenza GL. Regulation of Oxygen Homeostasis by Hypoxia-Inducible Factor 1. Physiology 2008; 24: 97-106.
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  • Talks KL, Turley H, Gatter KC, Maxwell PH, Pugh CW, Ratcliffe PJ, Harris AL. The expression and distribution of the hypoxia-inducible factors HIF-1 alpha and HIF-2alpha in normal human tissues, cancers, and tumor-associated macrophages. Am J Pathol 2000; 157: 411-421.
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Toplam 81 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Makaleler
Yazarlar

Saygın Hasan Demirel Bu kişi benim

Sümeyra Çetinkaya Bu kişi benim

Yayımlanma Tarihi 1 Aralık 2014
Gönderilme Tarihi 7 Eylül 2015
Yayımlandığı Sayı Yıl 2014

Kaynak Göster

AMA Demirel SH, Çetinkaya S. Hipoksiyle İndüklenen Faktör-1: Hücrenin Hipoksiye Fizyolojik ve Patolojik Cevabı. Sakarya Tıp Dergisi. Aralık 2014;4(4):171-177. doi:10.5505/sakaryamj.2014.15010

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