Gene expression profiling and bioinformatics analysis in 16HBE cells treated by chromium (VI)

被引:16
作者
Hu, Guiping [1 ]
Liu, Jiaxing [1 ]
Zhang, Yongming [2 ]
Zheng, Pai [3 ]
Wang, Lele [1 ]
Zhao, Lin [1 ]
Xu, Huadong [1 ]
Chen, Zhangjian [1 ]
Wang, Tiancheng [4 ]
Jia, Guang [1 ]
机构
[1] Peking Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth Sci, Beijing 100191, Peoples R China
[2] Baotou Med Coll, Sch Publ Hlth, Dept Occupat & Environm Hlth Sci, Baotou 014030, Inner Mongolia, Peoples R China
[3] Chinese Med Assoc, Editorial Dept Chinese Journal Prevent Med, Beijing 100710, Peoples R China
[4] Peking Univ, Dept Clin Lab, Hosp 3, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
Hexavalent chromium Cr (VI); Gene expression profile; Microarray analysis; Bioinformatics analysis; HEXAVALENT CHROMIUM; OXIDATIVE STRESS; CANCER; CHROMATE; WORKERS; CYTOTOXICITY; GENOTOXICITY; ACTIVATION; RESPONSES; TOXICITY;
D O I
10.1016/j.toxlet.2016.10.015
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Hexavalent chromium [Cr(VI)] compounds are widely used in industry and agriculture and are also ubiquitous environmental contaminant which are recognized as one kind of carcinogen, mutagen and teratogen towards humans and animals. To determined the Cr(VI) toxicity effects, gene expression profile can be meaningful for discovering underlying mechanisms of toxicity, and identifying potential specific genetic markers of Cr(VI) exposure and effects. In the current study, gene expression profiling and bioinformatics analysis in 16HBE cells treated by chromium(VI) compound were performed. The MTT assay was done to determine the optimal Cr(VI) treated concentration and time. The mRNA expression profile was performed using Arraystar Microarray V3.0 at 10.00 mu M Cr(VI). RT-qPCR was applied to verify some interested significantly altered genes at different treatment groups. Comprehensive analysis including biological processes, GO ontology network, pathway network analysis and gene-gene network analysis was conducted to identify the related biological processes, signal pathway and critical genes. It was found that Cr(VI) could induce reduced cells viability and alter gene expression profile of human bronchial epithelial cells. 2273 significantly differential expressed genes formed a complex network and some expressions changed in a Cr(VI) concentration dependent manner. In conclusion, Cr(VI) toxicity effects may involve in oxidative stress, inflammation, energy metabolism, protein synthesis endocytosis, ion binding, DNA binding and metabolism, cell morphogenesis, cell cycle regulation, autophagy, apoptosis, cell death, and carcinogenesis by some specific pathway. Meanwhile, some significantly differential expression genes can be used as potential biomarkers of Cr(VI) exposure. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
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