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  4. Biomonitoring of aristolactam-DNA adducts in human tissues using ultra-performance liquid chromatography/ion-trap mass spectrometry
 
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Biomonitoring of aristolactam-DNA adducts in human tissues using ultra-performance liquid chromatography/ion-trap mass spectrometry

Journal
Chemical Research in Toxicology
Journal Volume
25
Journal Issue
5
Pages
1119-1131
Date Issued
2012
Author(s)
Yun B.H.
Rosenquist T.A.
Sidorenko V.
Iden C.R.
CHUNG-HSIN CHEN  
YEONG-SHIAU PU  
Bonala R.
Johnson F.
Dickman K.G.
Grollman A.P.
Turesky R.J.
DOI
10.1021/tx3000889
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84861325737&doi=10.1021%2ftx3000889&partnerID=40&md5=716757b3cd2acf2aa9e7e4723b29d950
https://scholars.lib.ntu.edu.tw/handle/123456789/542098
Abstract
Aristolochic acids (AAs) are a structurally related family of nephrotoxic and carcinogenic nitrophenanthrene compounds found in Aristolochia herbaceous plants, many of which have been used worldwide for medicinal purposes. AAs have been implicated in the etiology of so-called Chinese herbs nephropathy and of Balkan endemic nephropathy. Both of these disease syndromes are associated with carcinomas of the upper urinary tract (UUC). 8-Methoxy-6-nitrophenanthro-[3,4-d] -1,3-dioxolo-5-carboxylic acid (AA-I) is a principal component of Aristolochia herbs. Following metabolic activation, AA-I reacts with DNA to form aristolactam (AL-I)-DNA adducts. We have developed a sensitive analytical method, using ultraperformance liquid chromatography-electrospray ionization/multistage mass spectrometry (UPLC-ESI/MSn) with a linear quadrupole ion-trap mass spectrometer, to measure 7-(deoxyadenosin-N6-yl) aristolactam I (dA-AL-I) and 7-(deoxyguanosin-N2-yl) aristolactam I (dG-AL-I) adducts. Using 10 μg of DNA for measurements, the lower limits of quantitation of dA-AL-I and dG-AL-I are, respectively, 0.3 and 1.0 adducts per 108 DNA bases. We have used UPLC-ESI/MSn to quantify AL-DNA adducts in tissues of rodents exposed to AA and in the renal cortex of patients with UUC who reside in Taiwan, where the incidence of this uncommon cancer is the highest reported for any country in the world. In human tissues, dA-AL-I was detected at levels ranging from 9 to 338 adducts per 108 DNA bases, whereas dG-AL-I was not found. We conclude that UPLC-ESI/MS n is a highly sensitive, specific and robust analytical method, positioned to supplant 32P-postlabeling techniques currently used for biomonitoring of DNA adducts in human tissues. Importantly, UPLC-ESI/MS n could be used to document exposure to AA, the toxicant responsible for AA nephropathy and its associated UUC. ? 2012 American Chemical Society.
SDGs

[SDGs]SDG3

Other Subjects
7(deoxyadenosin yl) 8 methoxy 6 nitrophenanthro [3,4 d] 1,3 dioxolo 5 carboxylic acid; aristololactam; DNA base; phosphorus 32; unclassified drug; adult; aged; animal tissue; article; biological monitoring; cancer patient; carcinogen DNA interaction; clinical article; controlled study; DNA adduct; female; human; human tissue; incidence; ion trap mass spectrometry; isotope labeling; kidney cortex; kidney disease; limit of quantitation; male; mass spectrometer; mouse; nonhuman; sensitivity and specificity; Taiwan; ultra performance liquid chromatography; urinary tract carcinoma; Adult; Aged; Animals; Aristolochia; Aristolochic Acids; Balkan Nephropathy; Chromatography, Liquid; DNA Adducts; Female; Humans; Kidney; Kidney Diseases; Limit of Detection; Male; Mice; Mice, Inbred C57BL; Middle Aged; Spectrometry, Mass, Electrospray Ionization; Aristolochia; Rodentia
Type
journal article

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