Expression of FOXO6 is Associated With Oxidative Stress Level and Predicts the Prognosis in Hepatocellular Cancer

Autor: Fu-Chun Yang, Shusen Zheng, Xiaofeng Xu, Yao-Min Chen, Hai-Yong Chen, Jian Wu, Zhen Lv
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
HBsAg
Pathology
Apoptosis
medicine.disease_cause
0302 clinical medicine
Cyclin D1
chemistry.chemical_classification
biology
Glutathione peroxidase
Liver Neoplasms
Forkhead Transcription Factors
Clinical Trial/Experimental Study
General Medicine
Middle Aged
Catalase
Prognosis
030220 oncology & carcinogenesis
Immunohistochemistry
Female
alpha-Fetoproteins
Liver cancer
Research Article
Adult
medicine.medical_specialty
Andrology
Superoxide dismutase
03 medical and health sciences
medicine
Humans
Aged
Cell Proliferation
Neoplasm Staging
Glutathione Peroxidase
Reactive oxygen species
Superoxide Dismutase
business.industry
medicine.disease
digestive system diseases
Oxidative Stress
030104 developmental biology
chemistry
Heme Oxygenase (Decyclizing)
biology.protein
Reactive Oxygen Species
business
Oxidative stress
Zdroj: Medicine
ISSN: 0025-7974
Popis: The aim of this study was to explore the association of Forkhead box O6 (FOXO6) expression with oxidative stress level and prognosis of hepatocellular cancer (HCC). The case group included tissues of HCC from 128 patients who were hospitalized in Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery of First Affiliated Hospital, School of Medicine, Zhejiang University. The control group included normal liver tissues from 74 patients. RT-PCR and Western blot were used to test expressions of FOXO6, heme oxygenase (HO)-1, glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT). Dihydroethidium (DHE) was dyed to observe reactive oxygen species (ROS) level. Immunohistochemistry was used to test FOXO6 expression. FOXO6 was silenced in HepG2 cells to detect cell proliferation and apoptosis. The expressions of ROS, HO-1, GPx, SOD, CAT, p27, and cyclin D1 were also detected to further explore the possible mechanism. The expressions of FOXO6, HO-1, GPx, SOD, and CAT in HCC tissue was significantly higher than those in normal and adjacent HCC tissues (P
Databáze: OpenAIRE