Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23501
Title: Methylation dependent gold adsorption behaviour identifies cancer derived extracellular vesicular DNA.
Austin Authors: Sina, Abu Ali Ibn;Lin, Ting-Yun;Vaidyanathan, Ramanathan;Wang, Zhaoran;Dey, Shuvashis;Wang, Jing;Behren, Andreas;Wuethrich, Alain;Carrascosa, Laura G;Trau, Matt
Affiliation: School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia
Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia
La Trobe School of Cancer Medicine, Heidelberg, Victoria, Australia
Centre for Personalised Nanomedicine, Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD 4072, Australia
Issue Date: 12-Jun-2020
Date: 2020-06-12
Publication information: Nanoscale horizons 2020; online first: 12 June
Abstract: Extracellular vesicles (EV) play a major role in intercellular communication by transmitting cellular materials (e.g. protein, RNA) among distant cells. Recent evidence suggests that they could also contribute to carrying DNA which could inform on the mutational status of the parent tumour DNA. Thus, the fundamental analysis of evDNA could open a better understanding of tumour metastasis and provide new pathways for noninvasive detection and monitoring of cancer. To explore the potential of evDNA for diagnostics, the isolation of pure evDNA from body fluids free of cfDNA contamination is crucial. Herein, we use a liposome based model system to develop an improved evDNA isolation protocol free from cfDNA contamination and evaluate the methylation dependent physicochemical properties of evDNA to develop a simple test for detecting cancer evDNA. Using a highly sensitive multiplex microelectrode device, we demonstrate that serum-evDNA derived from cancer patients show different solution and surface based properties than normal evDNA due to their different methylation landscape (i.e. methylscape). This microdevice allows simultaneous analysis of multiple samples in a single platform from as low as 500 pg μL-1 of evDNA.
URI: https://ahro.austin.org.au/austinjspui/handle/1/23501
DOI: 10.1039/d0nh00258e
ORCID: 0000-0001-8099-3863
0000-0003-3180-6202
0000-0001-6080-7998
0000-0001-5329-280X
0000-0001-9569-0478
0000-0001-9147-5658
0000-0001-5516-1280
Journal: Nanoscale horizons
PubMed URL: 32530449
Type: Journal Article
Appears in Collections:Journal articles

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