Chunyun Pu, Shaorong Tian, Sanxiu He, et al. Depression and stress levels increase risk of liver cancer through epigenetic downregulation of hypocretin. [J]. Genes & Diseases 9(4).(2022)
DOI:
Chunyun Pu, Shaorong Tian, Sanxiu He, et al. Depression and stress levels increase risk of liver cancer through epigenetic downregulation of hypocretin. [J]. Genes & Diseases 9(4).(2022) DOI: 10.1016/j.gendis.2020.11.013.
Depression and stress levels increase risk of liver cancer through epigenetic downregulation of hypocretin
摘要
Abstract
Recent studies suggest that Hypocretin (HCRT
Orexin) are involved in stress regulation of depression through the hypothalamic-pituitary-adrenal (HPA) axis. However
the molecular mechanism by which Hypocretin regulate neurobiological responses is unknown. Herein
the effects of chronic stress on the epigenetic modification of HCRT and its association with depression were explored with regard to a potential role in cancer progression. In the study
Sprague Dawley (SD) rats were used to establish an animal model of cancer with depression by administrating n-nitrosodiethylamine (DEN) and chronic unpredictable mild stress (CUMS). RNA-sequencing was used to detect differentially expressed genes in the hippocampus of rats and quantitative real-time polymerase chain reaction (qRT-PCR) was used to validate the results of RNA-sequencing. The status of HCRT promoter methylation was assessed by methylation specific polymerase chain reaction. Behavioral tests showed that rats exposed to CUMS had significant depressive-like behaviors. The number of liver tumors and tumor load in depressed rats exposed to CUMS was higher than in SD rats without CUMS. RNA-sequencing revealed that HCRT was one of the most siginificantly downregulated gene in the hippocampus of SD rats with CUMS compared to non-stressed group
which was validated by qRT-PCR. HCRT mRNA expression was downregulated and the promoter for HCRT was hyper-methylated in those with depression. These results identified a critical role for chronic psychological stressors in tumorigenesis and cancer progression
via epigenetic HCRT downregulation. Such epigenetic downregulation may be the molecular basis for the association of cancer with depression.