Dissemin is shutting down on January 1st, 2025

Published in

Springer, Applied Magnetic Resonance, 11(45), p. 1261-1273, 2014

DOI: 10.1007/s00723-014-0610-y

Links

Tools

Export citation

Search in Google Scholar

Superoxide- and NO-Dependent Mechanisms of the Reprogramming of Bone Marrow Cells by Tumor Cells

This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

EPR experiments in-vitro; spin trapping of the reactive oxygen / nitrogen species (superoxide radicals and nitric oxide, NO); gel zymography measurements in the tumor tissues, in the healthy and tumor affected bone marrow (BM) samples of rats are carried out. The superoxide and NO generation rates are derived; matrix metalloproteinases (MMP-2 and MMP-9) concentrations are measured. Their changes after the incubation with Guérin carcinoma cells at 37oC are defined. It is shown that the impact of tumor cells on BM manifests in the metabolic disorder, increased concentrations of active forms of MMP-2 and MMP-9, increased production of superoxide and NO radicals. Correlation between the appearance and intensity of the broad EPR signal at g = (2.2-2.4) with the concentrations of active forms of MMP-2 and MMP-9, NO and superoxide radicals’ rates is observed. The EPR signal may indicate the presence of distant metastases and may become a part of diagnostics. The obtained spatial and temporal changes of the EPR spectra demonstrate the usefulness of the potential application of EPR imaging to study the mechanisms of tumor invasion without a spin probe implementation. It is proposed that labile iron pool is responsible for the appearance of the EPR signal in tumor and BM samples.