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Published on: December 6, 2016
Exploring the genetic overlap between obstructive sleep apnea and prostate cancer
Allan Saj Porcacchia1, Mariana Moyses-Oliveira2, Gabriel Natan Pires1,2
1Departamento de Psicobiologia, Universidade Federal de São Paulo, São Paulo, Brazil.
Obstructive sleep apnea (OSA) and cancer share common genes, suggesting a linked molecular cause. This study identified 68 overlapping genes involved in hypoxia, cell damage, and proliferation, offering insights into their comorbidity.
Area of Science:
- Genetics
- Oncology
- Sleep Medicine
Background:
- Obstructive sleep apnea (OSA) is linked to increased cancer risk, particularly prostate cancer.
- The genetic overlap between OSA and cancer comorbidity requires further investigation.
- Understanding shared genetic factors is crucial for elucidating disease mechanisms.
Purpose of the Study:
- To identify shared risk genes between obstructive sleep apnea and cancer.
- To analyze the molecular pathways associated with these common genes.
- To explore the potential common molecular etiology underlying OSA-cancer comorbidity.
Main Methods:
- Identified genes common to both OSA and cancer.
- Assessed the statistical significance of the gene overlap.
- Performed pathway enrichment and protein-protein interaction analyses on the intersecting gene set.
Main Results:
- Identified 68 common genes between OSA and cancer, a number exceeding random chance.
- The shared gene list was significantly associated with pathways related to hypoxia, apoptosis, oxidative stress, and cell cycle proliferation/damage.
- A 17-node protein interaction network revealed key proteins within these enriched pathways.
Conclusions:
- A common molecular etiology underlies the comorbidity of OSA and cancer.
- Enriched pathways including proliferation, apoptosis, and hypoxia suggest their critical role in the shared pathophysiological processes.
- These findings provide a molecular basis for the observed association between OSA and cancer risk.
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