Up-down regulation of HIF-1α in cancer progression
•HIF-1α stimulate cancer progression through angiogenesis, metastasis, cell proliferation and metabolism alternation process.•HIF-1α has important role during cancer progression through simulation of genetic instability.•Inhibition of HIF-1α has promising result in cancer treatment. Hypoxia induicib...
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Veröffentlicht in: | Gene 2021-09, Vol.798, p.145796-145796, Article 145796 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •HIF-1α stimulate cancer progression through angiogenesis, metastasis, cell proliferation and metabolism alternation process.•HIF-1α has important role during cancer progression through simulation of genetic instability.•Inhibition of HIF-1α has promising result in cancer treatment.
Hypoxia induicible factor-1 alpha (HIF-1α) is a key transcription factor in cancer progression and target therapy in cancer. HIF-1α acts differently depending on presence or absence of Oxygen. In an oxygen-immersed environment, HIF-1α completely deactivated and destroyed by the ubiquitin proteasome pathway (UPP). In contrast, in the oxygen-free environment, it escapes destruction and enters to the nucleus of cells then upregulates many genes involved in cancer progression. Overexpressed HIF-1α and downstream genes support cancer progression through various mechanisms including angiogenesis, proliferation and survival of cells, metabolism reprogramming, invasion and metastasis, cancer stem cell maintenance, induction of genetic instability, and treatment resistance. HIF-1α can be provoked by signaling pathways unrelated to hypoxia during cancer progression. Therefore, cancer development and progression can be modulated by targeting HIF-1α and its downstream signaling molecules. In this regard, HIF-1α inhibitors which are categorized into the agents that regulate HIF-1α in gene, mRNA and protein levels used as an efficient way in cancer treatment. Also, HIF-1α expression can be negatively affected by the agents suppressing the activation of mTOR, PI3k/Akt and MAPK pathways. |
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ISSN: | 0378-1119 1879-0038 |
DOI: | 10.1016/j.gene.2021.145796 |