Aristolochic Acid Suppresses DNA Repair and Triggers Oxidative DNA Damage in Human Kidney Proximal Tubular Cells
Resource
ONCOLOGY REPORTS v.24 n.1 pp.141-153
Journal
Toxicology Letters
Pages
S62
Date Issued
2010
Date
2010
Author(s)
CHEN, YA-YIN
CHUNG, JING-GUNG
WU, HSIU-CHING
BAU, DA-TIAN
WU, KUEN-YUH
KAO, SHUNG-TE
HSIANG, CHIEN-YUN
HO, TIN-YUN
CHIANG, SU-YIN
Abstract
Aristolochic acid (AA), derived from plants of the Aristolochia genus, has been proven to be associated with aristolochic acid nephropathy (AAN) and urothelial cancer in AAN patients. In this study, we used toxicogenomic analysis to clarify the molecular mechanism of AA-induced cytotoxicity in normal human kidney proximal tubular (HK-2) cells, the target cells of AA. AA induced cytotoxic effects in a dose-dependent (10, 30, 90 mu M for 24 h) and time- dependent manner (30 mu M for 1, 3, 6, 12 and 24 h). The cells from those experiments were then used for microarray experiments in triplicate. Among the differentially expressed genes analyzed by Limma and Ingenuity Pathway Analysis software, we found that genes in DNA repair processes were the most significantly regulated by all AA treatments. Furthermore, response to DNA damage stimulus, apoptosis, and regulation of cell cycle, were also significantly regulated by AA treatment. Among the differentially expressed genes found in the dose- response and time-course studies that were involved in these biological processes, two up-regulated (GADD45B, NAIP), and six down-regulated genes (TP53, PARPI, OGG1, ERCC1, ERCC2, and MGMT) were confirmed by quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR). AA exposure also caused a down-regulation of the gene expression of antioxidant enzymes, such as superoxide dismutase, glutathione reductase, and glutathione peroxidase . Moreover, AA treatment led to increased frequency of DNA strand breaks, 8-hydroxydeoxyguanosine-positive nuclei, and micronuclei in a dose-dependent manner in HK-2 cells, possibly as a result of the inhibition of DNA repair. These data suggest that oxidative stress plays a role in the cytotoxicity of AA. In addition, our results provide insight into the involvement of down-regulation of DNA repair gene expression as a possible mechanism for AA-induced genotoxicity.
Subjects
aristolochic acid
DNA repair
oxidative DNA damage
SDGs
Type
journal article