| Literature DB >> 27446474 |
Barbora Fecková1, Patrícia Kimáková1, Lenka Ilkovičová1, Erika Szentpéteriová1, Nataša Debeljak2, Zuzana Solárová3, Veronika Sačková1, Martina Šemeláková1, Mangesh Bhide4, Peter Solár1.
Abstract
The erythropoietin receptor (EpoR) is a member of the cytokine receptor family. The interaction between erythropoietin (Epo) and EpoR is important for the production and maturation of erythroid cells, resulting in the stimulation of hematopoiesis. The fact that EpoR was also detected in neoplastic cells has opened the question about the relevance of anemia treatment with recombinant Epo in cancer patients. Numerous studies have reported pro-stimulating and anti-apoptotic effects of Epo in cancer cells, thus demonstrating EpoR functionality in these cells. By contrast, a previous study claims the absence of EpoR in tumor cells. This apparent discrepancy is based, according to certain authors, on the use of non-specific anti-EpoR antibodies. With the aim of bypassing the direct detection of EpoR with an anti-EpoR antibody, the present authors propose a far-western blot methodology, which in addition, confirms the interaction of Epo with EpoR. Applying this technique, the presence of EpoR and its interaction with Epo in human ovarian adenocarcinoma A2780 and normal human umbilical vein endothelial cells was confirmed. Furthermore, modified immunoprecipitation of EpoR followed by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry analysis confirmed a 57 kDa protein as a human Epo-interacting protein in both cell lines.Entities:
Keywords: A2780; HUVEC; erythropoietin; erythropoietin receptor; far-western blotting
Year: 2016 PMID: 27446474 PMCID: PMC4950567 DOI: 10.3892/ol.2016.4782
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967