Altered gene expression in human hepatoma HepG2 cells exposed to low-level 2,4-dichlorophenoxyacetic acid and potassium nitrate

被引:21
|
作者
Bharadwaj, L
Dhami, K
Schneberger, D
Stevens, M
Renaud, C
Ali, A
机构
[1] Univ Saskatchewan, Inst Agr Rural & Environm Hlth, Dept Med & Toxicol Grp, Saskatoon, SK S7N 0W8, Canada
[2] Univ Windsor, Dept Biol Sci, Windsor, ON N9B 3P4, Canada
关键词
herbicides; 2,4-D; nitrate; groundwater; HepG2; cells; gene expression profiling; cytotoxicity; DNA microarray;
D O I
10.1016/j.tiv.2005.03.011
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
2,4-Dichlorophenoxyacetic acid (2,4-D) and nitrate are agricultural contaminants found in rural ground water. It is not known whether levels found in groundwater pose a human or environmental health risk, nor is the mechanism of toxicity at the molecular/ cellular level understood. This study focused on determining whether 2,4-D or nitrate at environmentally realistic levels elicit gene expression changes in exposed cells. cDNA microarray technology was used to determine the impact of 2,4-D and nitrate in an in vitro model of exposure. Human hepatoma HepG2 cells were incubated with 2,4-D or nitrate alone for 24 h. Cell viability (neutral red assay) and proliferation (BrdU incorporation) were assessed following exposure. Total RNA from treated and control cells were isolated, reverse transcribed and reciprocal labelled with Cy3 or Cy5 dyes, and hybridized to a human cDNA microarray. The hybridized microarray chips were scanned, quantified and analyzed to identify genes affected by 2,4-D or nitrate exposure based on a two-fold increase or decrease in gene expression and reproducibility (affected in three or more treatments). Following filtering, normalization and hierarchical clustering initial data indicate that numerous genes were found to be commonly expressed in at least three or more treatments of 2,4-D or nitrate tested. The affected genes indicate that HepG2 cells respond to environmental, low-level exposure and produce a cellular response that is associated with alterations in the expression of many genes. The affected genes were characterized as stress response, cell cycle control, immunological and DNA repair genes. These findings serve to highlight new pathway(s) in which to further probe the effects of environmental levels of 2,4-D and nitrate. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:603 / 619
页数:17
相关论文
共 50 条
  • [41] GLUTATHIONE S-TRANSFERASES PREDOMINANTLY ACCUMULATE IN PUMPKIN CULTURE CELLS EXPOSED TO EXCESSIVE CONCENTRATIONS OF 2,4-DICHLOROPHENOXYACETIC ACID
    FUJITA, M
    ADACHI, Y
    HANADA, Y
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1995, 59 (09) : 1721 - 1726
  • [42] Severe hypoxia specifically downregulates hepatocyte nuclear factor-4 gene expression in HepG2 human hepatoma cells
    Mazure, NM
    Trong, LN
    Danan, JL
    TUMOR BIOLOGY, 2001, 22 (05) : 310 - 317
  • [43] Expression of the p53 human tumor suppressor gene is altered by zinc status in HepG2 cells.
    Reaves, SK
    Wu, JYJ
    Wang, YR
    Fanzo, JC
    Lei, KY
    FASEB JOURNAL, 1997, 11 (03): : 1122 - 1122
  • [44] The effect of abnormal Savda Munziq total flavonoids on the proliferation, apoptosis and correlative gene expression in human hepatoma (HepG2) cells
    Yusup, Abdiryim
    Upur, Halmurat
    Tursun, Xirali
    Berke, Benedicte
    Baudrimont, Isabelle
    Moore, Nicholas
    TOXICOLOGY LETTERS, 2006, 164 : S250 - S250
  • [45] cDNA-AFLP analysis of differential gene expression in human hepatoma cells (HepG2) upon dengue virus infection
    Ekkapongpisit, Maneerat
    Wannatung, Tirawat
    Susantad, Tharinee
    Triwitayakorn, Kanokporn
    Smith, Duncan R.
    JOURNAL OF MEDICAL VIROLOGY, 2007, 79 (05) : 552 - 561
  • [46] LIPOPOLYSACCHARIDE-BINDING PROTEIN EXPRESSION IN PRIMARY HUMAN HEPATOCYTES AND HEPG2 HEPATOMA-CELLS
    GRUBE, BJ
    COCHRANE, CG
    YE, RD
    GREEN, CE
    MCPHAIL, ME
    ULEVITCH, RJ
    TOBIAS, PS
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1994, 269 (11) : 8477 - 8482
  • [47] Regulation of angiogenin expression in human HepG2 hepatoma cells by mediators of the acute-phase response
    Verselis, SJ
    Olson, KA
    Fett, JW
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 259 (01) : 178 - 184
  • [48] Effects of the rodent peroxisome proliferator and hepatocarcinogen, perfluorooctanoic acid, on apoptosis in human hepatoma HepG2 cells
    Shabalina, IG
    Panaretakis, T
    Bergstrand, A
    DePierre, JW
    CARCINOGENESIS, 1999, 20 (12) : 2237 - 2246
  • [49] Sulfasalazine inhibits bile acid-induced apoptosis in human HepG2 hepatoma cells.
    Rust, C
    Vennegerts, T
    Bauchmuller, K
    Betters, U
    HEPATOLOGY, 2002, 36 (04) : 324A - 324A
  • [50] Dihydromyricetin Reduced Bcl-2 Expression via p53 in Human Hepatoma HepG2 Cells
    Wu, Shixing
    Liu, Bin
    Zhang, Qingyu
    Liu, Jie
    Zhou, Wei
    Wang, Chang
    Li, Mingyi
    Bao, Shiting
    Zhu, Runzhi
    PLOS ONE, 2013, 8 (11):