Extracellular plasma RNA from colon cancer patients is confined in a vesicle-like structure and is mRNA-enriched

  1. José Miguel García1,4,
  2. Vanesa García1,4,
  3. Cristina Peña1,
  4. Gemma Domínguez1,
  5. Javier Silva1,
  6. Raquel Diaz1,
  7. Pablo Espinosa1,
  8. Maria Jesús Citores2,
  9. Manuel Collado3, and
  10. Félix Bonilla1
  1. 1Department of Medical Oncology, Hospital Universitario Puerta de Hierro, E-28035 Madrid, Spain
  2. 2Department of Tumor Immunology, Hospital Universitario Puerta de Hierro, E-28035 Madrid, Spain
  3. 3Tumor Suppression Group, Spanish National Cancer Centre (CNIO), E-28029 Madrid, Spain
  1. 4 These authors contributed equally to this work.

Abstract

Little is yet known about the origin and protective mechanism of free nucleic acids in plasma. We investigated the possibility of these free nucleic acids being particle associated. Plasma samples from colon cancer patients and cell culture media were subjected to various antibody incubations, ultracentrifugation, and RNA extraction protocols for total RNA, epithelial RNA, and mRNA. Flow cytometry using a Ber-EP4 antibody and confocal laser microscopy after staining with propidium iodide were also performed. mRNA levels of the LISCH7 and SDHA genes were determined in cells and in culture media. Ber-EP4 antibody and polystyrene beads coated with oligo dT sequences were employed. We observed that, after incubation, total RNA and mRNA were always detected after membrane digestion, and that epithelial RNA was detected before this procedure. In ultracentrifugation, mRNA was caught in the supernatant only if a former lysis mediated or in the pellet if there was no previous digestion. Flow cytometry determinations showed that antibody-coated microbeads keep acellular structures bearing epithelial antigens apart. Confocal laser microscopy made 1- to 2-μm-diameter particles perceptible in the vicinity of magnetic polystyrene beads. Relevant differences were observed between mRNA of cells and culture media, as there was a considerable difference in LISCH7 mRNA levels between HT29 and IMR90 cell co-cultures and their culture media. Our results support the view that extracellular RNA found in plasma from cancer patients circulates in association with or is protected in a multiparticle complex, and that an active release mechanism by tumor cells may be a possible origin.

Keywords

Footnotes

  • Reprint requests to: Félix Bonilla, Department of Medical Oncology, Hospital Universitario Puerta de Hierro, C/ San Martín de Porres, 4, E-28035 Madrid, Spain; e-mail: fbonilla.hpth{at}salud.madrid.org; fax: 34-91-3445189.

  • Abbreviations: Ab, antibody; DEE, Dynabeads Epithelial Enrich; DMEM, Dulbecco modified Eagle medium; FCS, fetal calf serum; FITC, fluorescein isothiocyanate; LISCH7, liver-specific bHLH-Zip transcription factor; PBS, phosphate-buffered saline; PCR, polymerase chain reaction; PE, phycoerytrin; PI, propidium iodide; QRT-PCR, real-time PCR; RT, room temperature; SDHA, succinate dehydrogenase complex subunit A.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.755908.

    • Received July 25, 2007.
    • Accepted March 17, 2008.
| Table of Contents