2008
DOI: 10.1289/ehp.6249
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Genomic and Proteomic Profiling of Responses to Toxic Metals in Human Lung Cells

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Cited by 54 publications
(70 citation statements)
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References 23 publications
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“…Previous studies showed that the expression of HSP90 at the transcriptional level varied greatly in different species responding to different heavy metal stress. For instance, HSP90a gene expression in human lung cells was up-regulated by As (5 or 50 lmol/L), while down-regulated by heavy metals such as Cd (3 lmol/L), Ni (3 lg/cm 2 ), and Cr (10 lmol/L) (Andrew et al 2003). HSP90a in common carp liver was up-regulated when the fish were kept in water containing 10 mg/L Cd, while in the kidney, it was up-regulated and reached a peak then down-regulated (Hermesz et al 2001).…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies showed that the expression of HSP90 at the transcriptional level varied greatly in different species responding to different heavy metal stress. For instance, HSP90a gene expression in human lung cells was up-regulated by As (5 or 50 lmol/L), while down-regulated by heavy metals such as Cd (3 lmol/L), Ni (3 lg/cm 2 ), and Cr (10 lmol/L) (Andrew et al 2003). HSP90a in common carp liver was up-regulated when the fish were kept in water containing 10 mg/L Cd, while in the kidney, it was up-regulated and reached a peak then down-regulated (Hermesz et al 2001).…”
Section: Discussionmentioning
confidence: 99%
“…Thangaradjou et al [39] reported interspecific and intraspecific differences in the accumulation of different metals (Mn, Al, Fe, Cr, Cu, Zn, Pb, Cd, Co and Ni) in seagrasses of Andaman Islands. The presence of heavy metals in food and medicinal plants may cause severe health problems including renal failure, chronic toxicity and liver damage [44][45][46]. According to the World Health Organization [47], the concentration of heavy metals must be controlled in medicinal plants in order to meet the quality assurance.…”
Section: Introductionmentioning
confidence: 99%
“…Consequently, arsenic may act on stem or progenitor cells of the bronchial epithelium by altering the expression of genes involved in key regulatory pathways. Indeed, arsenic has been shown to inhibit protein tyrosine and serine/threonine phosphatases, regulatory enzymes that often carry a thiol group in their active center, and to alter the expression of many kinases implicated in signaling pathways (Andrew et al 2003;Cavigelli et al 1996;Huang et al 1995;Tapio et al 2005). In line with this, large-scale expression analysis revealed that speciWc lung developmental pathways are reactivated in NSCLC (Borczuk et al 2003).…”
Section: Discussionmentioning
confidence: 99%