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Circulating Nucleic Acids in Plasma/Serum and Tumor Progression
Author(s) -
SAMOS JULIA,
GARCÍAOLMO DOLORES C.,
PICAZO MARÍA G.,
RUBIOVITALLER ANTONIO,
GARCÍAOLMO DAMIÁN
Publication year - 2006
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1368.022
Subject(s) - nucleic acid , propidium iodide , apoptosis , flow cytometry , annexin , cancer , chemistry , dna , cancer research , microbiology and biotechnology , biology , pathology , programmed cell death , biochemistry , medicine , genetics
Abstract: The “genometastasis hypothesis” proposes that cell‐free tumor nucleic acids might be able to transform host stem cells, and that this might be a pathway for the development of metastases. This theory is supported by previous experimental findings and is consistent with observations of other authors. It has been suggested that tumor DNA might be horizontally transferred by the uptake of apoptotic bodies and initiate the genetic changes that are necessary for tumor formation. In addition, apoptotic bodies have been proposed as possible vehicles that protect the nucleic acids circulating in the plasma from enzymatic degradation. In the present study, we analyzed the presence of apoptotic bodies in serum and its relationship with tumor progression in a heterotopic model of colon cancer in the rat. We injected DHD/K12‐PROb cancer cells subcutaneously into BD‐IX rats and divided the animals into three groups according to the time between the injection of tumor cells and euthanasia. A control group of healthy animals was included ( n = 6). After euthanasia, macroscopic metastases were assessed and samples of blood were collected. To detect apoptotic bodies in the sera, each sample was mixed with FITC‐conjugated annexin V antibody in combination with propidium iodide and then analyzed by flow cytometry. Detection of apoptotic bodies was only significantly increased in the sera of a few tumor‐bearing animals in late stages of tumor development. Thus, such particles appear not to be the vehicle of the cell‐free tumor nucleic acids that are detected at early stages of cancer.