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Profiling of Gene Expression in Human Keratinocyte Cell Line Exposed to Quantum Dot Nanoparticles

Authors
Kim, In-KyoungLee, Seung-HoKim, Yu-RiSeo, Sang-HuiJeong, Sang HoonSon, Sang WookKim, Meyoung-Kon
Issue Date
31-3월-2009
Publisher
KOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT
Keywords
Quantum dot; cDNA microarray; PCR array; Keratinocyte
Citation
MOLECULAR & CELLULAR TOXICOLOGY, v.5, no.1, pp.51 - 57
Indexed
SCIE
KCI
OTHER
Journal Title
MOLECULAR & CELLULAR TOXICOLOGY
Volume
5
Number
1
Start Page
51
End Page
57
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/120401
ISSN
1738-642X
Abstract
Quantum Dot (QD) nanoparticles are used in various industrial applications, such as diagnostic, drug delivery, and imaging agents of biomedicine. Although QDs are extensively used in many medical science, several studies have been demonstrated the potential toxicity of nanoparticles. The first objective of this study was to investigate the nanotoxicity of QDs in the HaCaT human keratinocyte cell line by focusing on gene expression pattern. In order to evaluate the effect of QDs on gene expression profile in HaCaT cells, we analyzed the differential genes which related to oxidative stress and antioxidant defense mechanisms by using human cDNA microarray and PCR array. A human cDNA microarray was clone set, which was sorted for a list of genes correlated with cell mechanisms. We tried to confirm results of cDNA microarray by using PCR array, which is pathway-focused gene expression profiling technology using Real-Time PCR. Although we could not find the exactly same genes in both methods, we have screened the effects of QDs on global gene expression profiles in human skin cells. In addition, our results show that QD treatment somehow regulates cellular pathways of oxidative stress and antioxiclant defense mechanisms. Therefore, we suggest that this study can enlarge our knowledge of the transcriptional profile and identify new candidate biomarker genes to evaluate the toxicity of nanotoxicology.
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