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Chromatography 2016

September 21-23, 2016

Volume 7, Issue 5(Suppl)

J Chromatogr Sep Tech 2016

ISSN: 2157-7064 JCGST, an open access journal

conferenceseries

.com

September 21-23, 2016 Amsterdam, Netherlands

World Congress on

Chromatography

A link between aberrant methylation level and AA adducts: Fact or coincidence

Dalia El-Zeihery

1

, Mohamed Abd El Kawy

1

, Oliver Schmitz

2

, Cai Zongwei

3

and Heinz Schmeiser

4

1

Beni-Suef University, Egypt

2

Essen-Duisburg University, Germany

3

Hong Kong Baptist University, China

4

German Cancer Research Center, Germany

T

hemainaimof this study istoestimate theeffectof aristolochicacid(AA)onthegenomicmethylationlevel (5-methylcytosine,

5mc) of Sprague-Dawley rats subjected to a single oral dose of 30 mg AA/kg over three weeks-period, and to detect AA-

DNA adducts in tissues of rodents. Our analytical method involves hydrolyzing the DNA extracted from different organs to

2-deoxyribose-3’-phosphate, labeling the nucleotides with a fluorescence marker, thenmeasuring the genome wide methylation

level with micellar electrokinetic chromatography using laser-induced fluorescence detector (MEKC-LIF). The results had

shown different behavior patterns in the methylation level according to the tested organ. An obvious hypermethylation was

observed in kidney, stomach and colon of rats dosed with AA, in comparison with their respective controls. Individual 5mc

levels are (3.97±0.05, 3.90±0.04 and 4.46±0.04%) for organs, respectively. Bladder, small intestine and liver did not exhibit

either hyper- or hypo- methylation. We further studied the samples for detection of AA-adducts in two complementary studies.

The deoxyadenosine-AA-adducts were identified in kidney (Adduct level, 2.63 to 5.16/10

6

nucleotides) and colon tissues (0.28

to 1.01/106 nucleotides) among several tissues analyzed by the

32

P-postlabeling method. While control samples were free from

DNA adducts spots. As well, the highest AA-DNA adduct concentration was detected in kidneys of the AA-dosed rats by

LC-ESI-MS method. Our study highlights the relation between the exposure to this carcinogen belonging to natural product

group (AA) and the aberration of methylation level that contributes to understanding the involvement of AA-adducts in cancer

development via epigenetic modification.

Biography

Dalia Mohamed El-Zeihery received her PhD from the Bergische Universitaet Wuppertal in Germany and completed Post-doctoral studies at CRO in Germany.

She is lecturer of Analytical Chemistry at Beni Suef University in Egypt. She has strong footing in teaching and research, in depth theoretical knowledge and

hands-on experience in analytical techniques: like capillary electrophoresis, HPLC-MS and UV-VIS spectroscopy. She was awarded third prize of Pharmaceutical

and Bio-analysis from Pfizer for her poster at the 2009 34th International Symposium on HPLC Separations and Related Techniques. His research interests are

development and validation of bio-analytical methods for analysis of drugs, proteins and biomarkers.

dzehery@yahoo.com

Dalia El-Zeihery et al., J Chromatogr Sep Tech 2016, 7:5(Suppl)

http://dx.doi.org/10.4172/2157-7064.C1.017