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World J Clin Oncol. Jul 10, 2012; 3(7): 104-110
Published online Jul 10, 2012. doi: 10.5306/wjco.v3.i7.104
Published online Jul 10, 2012. doi: 10.5306/wjco.v3.i7.104
Figure 1 Hypoxia induced regulation of N-Myc down-regulated gene 1 in human brain cancer hypoxia-inducible factor-1α induced regulation of hypoxia induced N-Myc down-regulated gene 1 expression in human tumour cells.
A: Under normoxic oxygenation conditions in the tumor cell microenvironment, hypoxia-inducible factor (HIF)-1α is rapidly degraded via the von Hippel-Lindau tumour suppressor gene product (pVHL)-mediated ubiquitin proteasome pathway; B: When the tumor environment aeration conditions shifts from normoxic to hypoxic aeration conditions, HIF-1α subunit becomes stable, translocates into the cellular nucleus and interacts with co-activators of which its transcription machinery is consisted such as p300/CBP to modulate the transcriptional activity of numerous hypoxia inducible genes, like N-Myc down-regulated gene 1 (NDRG1) in the case and about 61 other hypoxia induced genes[28,40]. HRE: Hypoxia response element.
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Citation: Said HM, Polat B, Stein S, Guckenberger M, Hagemann C, Staab A, Katzer A, Anacker J, Flentje M, Vordermark D. Inhibition of N-Myc down regulated gene 1 in
in vitro cultured human glioblastoma cells. World J Clin Oncol 2012; 3(7): 104-110 - URL: https://www.wjgnet.com/2218-4333/full/v3/i7/104.htm
- DOI: https://dx.doi.org/10.5306/wjco.v3.i7.104