Hypoxia‐induced alterations of G2 checkpoint regulators. Issue 5 (8th January 2016)
- Record Type:
- Journal Article
- Title:
- Hypoxia‐induced alterations of G2 checkpoint regulators. Issue 5 (8th January 2016)
- Main Title:
- Hypoxia‐induced alterations of G2 checkpoint regulators
- Authors:
- Hasvold, Grete
Lund-Andersen, Christin
Lando, Malin
Patzke, Sebastian
Hauge, Sissel
Suo, ZhenHe
Lyng, Heidi
Syljuåsen, Randi G. - Abstract:
- Abstract : Hypoxia promotes an aggressive tumor phenotype with increased genomic instability, partially due to downregulation of DNA repair pathways. However, genome stability is also surveilled by cell cycle checkpoints. An important issue is therefore whether hypoxia also can influence the DNA damage‐induced cell cycle checkpoints. Here, we show that hypoxia (24 h 0.2% O2) alters the expression of several G2 checkpoint regulators, as examined by microarray gene expression analysis and immunoblotting of U2OS cells. While some of the changes reflected hypoxia‐induced inhibition of cell cycle progression, the levels of several G2 checkpoint regulators, in particular Cyclin B, were reduced in G2 phase cells after hypoxic exposure, as shown by flow cytometric barcoding analysis of individual cells. These effects were accompanied by decreased phosphorylation of a Cyclin dependent kinase (CDK) target in G2 phase cells after hypoxia, suggesting decreased CDK activity. Furthermore, cells pre‐exposed to hypoxia showed increased G2 checkpoint arrest upon treatment with ionizing radiation. Similar results were found following other hypoxic conditions (∼0.03% O2 20 h and 0.2% O2 72 h). These results demonstrate that the DNA damage‐induced G2 checkpoint can be altered as a consequence of hypoxia, and we propose that such alterations may influence the genome stability of hypoxic tumors. Highlights: The G2 checkpoint can be altered as a consequence of hypoxia. Flow cytometry barcodingAbstract : Hypoxia promotes an aggressive tumor phenotype with increased genomic instability, partially due to downregulation of DNA repair pathways. However, genome stability is also surveilled by cell cycle checkpoints. An important issue is therefore whether hypoxia also can influence the DNA damage‐induced cell cycle checkpoints. Here, we show that hypoxia (24 h 0.2% O2) alters the expression of several G2 checkpoint regulators, as examined by microarray gene expression analysis and immunoblotting of U2OS cells. While some of the changes reflected hypoxia‐induced inhibition of cell cycle progression, the levels of several G2 checkpoint regulators, in particular Cyclin B, were reduced in G2 phase cells after hypoxic exposure, as shown by flow cytometric barcoding analysis of individual cells. These effects were accompanied by decreased phosphorylation of a Cyclin dependent kinase (CDK) target in G2 phase cells after hypoxia, suggesting decreased CDK activity. Furthermore, cells pre‐exposed to hypoxia showed increased G2 checkpoint arrest upon treatment with ionizing radiation. Similar results were found following other hypoxic conditions (∼0.03% O2 20 h and 0.2% O2 72 h). These results demonstrate that the DNA damage‐induced G2 checkpoint can be altered as a consequence of hypoxia, and we propose that such alterations may influence the genome stability of hypoxic tumors. Highlights: The G2 checkpoint can be altered as a consequence of hypoxia. Flow cytometry barcoding reveals reduction of G2 checkpoint proteins after hypoxia. Cyclin B expression and CDK activity were reduced in G2 phase cells after hypoxia. Radiation‐induced G2 checkpoint arrest was increased after hypoxia. Hypoxia‐induced alterations of the G2 checkpoint may affect genome stability. … (more)
- Is Part Of:
- Molecular oncology. Volume 10:Issue 5(2016:May)
- Journal:
- Molecular oncology
- Issue:
- Volume 10:Issue 5(2016:May)
- Issue Display:
- Volume 10, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 10
- Issue:
- 5
- Issue Sort Value:
- 2016-0010-0005-0000
- Page Start:
- 764
- Page End:
- 773
- Publication Date:
- 2016-01-08
- Subjects:
- Hypoxia -- G2 checkpoint -- DNA damage -- Ionizing radiation -- Genome stability
Cancer -- Molecular aspects -- Periodicals
616.994005 - Journal URLs:
- http://www.journals.elsevier.com/molecular-oncology/ ↗
http://febs.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1878-0261/issues/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molonc.2015.12.015 ↗
- Languages:
- English
- ISSNs:
- 1574-7891
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817993
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- 9339.xml