Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/105406
Title: Tumor circulating DNA profiling in xenografted mice exposed to intermittent hypoxia.
Author: Cortese, Rene
Almendros López, Isaac
Wang, Yang
Gozal, David
Keywords: Síndromes d'apnea del son
Anoxèmia
Càncer
Reacció en cadena de la polimerasa
Rates (Animals de laboratori)
Sleep apnea syndromes
Anoxemia
Cancer
Polymerase chain reaction
Rats as laboratory animals
Issue Date: 1-Jan-2015
Publisher: Impact Journals
Abstract: Intermittent hypoxia (IH) a hallmark characteristic of obstructive sleep apnea (OSA), is proposed as a major determinant of processes involving tumor growth, invasion and metastasis. To examine whether circulating DNA (cirDNA) in blood plasma reflects changes in tumor cells under IH conditions, we used a xenografted murine model. Mice engrafted with TC1 epithelial lung cancer cells and controls were exposed to IH or room air (RA) conditions. Plasma cirDNA amounts were significantly increased in mice exposed to IH (p<0.05). Significant associations between plasma cirDNA concentrations and tumor size, weight and invasiveness also emerged (p<0.05). Using a methylation microarray-based approach, we identified 2,094 regions showing significant differential cirDNA modifications. Systems biology analyses revealed an association with molecular pathways deregulated in cancer progression and with distal and TSS-associated transcription factor binding sites. We detected clusters of highly variable regions in chromosomes 7, 13, 14 and X, which may highlight hotspots for DNA deletions. Single locus displayed high intragroup variation, suggesting cellular heterogeneity within the tissue may be associated to cirDNA release. Thus, exposures to IH increase the shedding of cirDNA into circulation, which carries epigenetic modifications that may characterize cell populations within the tumor that preferentially release their DNA upon IH exposure.
Note: Reproducció del document publicat a: https://doi.org/10.18632/oncotarget.2785
It is part of: Oncotarget, 2015, vol. 6, num. 1, p. 556-569
Related resource: https://doi.org/10.18632/oncotarget.2785
URI: http://hdl.handle.net/2445/105406
ISSN: 1949-2553
Appears in Collections:Articles publicats en revistes (Biomedicina)

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