Circulating Cell-Free DNA in Dogs with Mammary Tumors: Short and Long Fragments and Integrity Index

PLoS One. 2017 Jan 12;12(1):e0169454. doi: 10.1371/journal.pone.0169454. eCollection 2017.

Abstract

Circulating cell-free DNA (cfDNA) has been considered an interesting diagnostic/prognostic plasma biomarker in tumor-bearing subjects. In cancer patients, cfDNA can hypothetically derive from tumor necrosis/apoptosis, lysed circulating cells, and some yet unrevealed mechanisms of active release. This study aimed to preliminarily analyze cfDNA in dogs with canine mammary tumors (CMTs). Forty-four neoplastic, 17 non-neoplastic disease-bearing, and 15 healthy dogs were recruited. Necrosis and apoptosis were also assessed as potential source of cfDNA on 78 CMTs diagnosed from the 44 dogs. The cfDNA fragments and integrity index significantly differentiated neoplastic versus non-neoplastic dogs (P<0.05), and allowed the distinction between benign and malignant lesions (P<0.05). Even if without statistical significance, the amount of cfDNA was also affected by tumor necrosis and correlated with tumor size and apoptotic markers expression. A significant (P<0.01) increase of Bcl-2 in malignant tumors was observed, and in metastatic CMTs the evasion of apoptosis was also suggested. This study, therefore, provides evidence that cfDNA could be a diagnostic marker in dogs carrying mammary nodules suggesting that its potential application in early diagnostic procedures should be further investigated.

MeSH terms

  • Animals
  • DNA, Neoplasm / blood*
  • DNA, Neoplasm / genetics
  • Dog Diseases / blood*
  • Dog Diseases / diagnosis
  • Dog Diseases / genetics
  • Dogs
  • Female
  • Mammary Neoplasms, Animal / blood*
  • Mammary Neoplasms, Animal / diagnosis
  • Mammary Neoplasms, Animal / genetics
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism

Substances

  • DNA, Neoplasm
  • Proto-Oncogene Proteins c-bcl-2

Grants and funding

G. Beffagna was supported by a fellowship from the Umberto Veronesi Foundation Young Investigator Research Programme. The activity in MC laboratory was supported by the BBSRC New Investigator Award Grant (BB/I013695/1), PPCT, LAM Research Grant on Brain Tumours, FP7-PEOPLE-2011-CIG. One of the authors (Andrea Saccani) is employed by the commercial company Euroclone. However, the authors declare that the funder provided support in the form of salary for author [A. Saccani] and provided support in the form of materials for qPCR (Master mix, probe and primers), but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of this author are articulated in the ‘author contributions’ section.