Fecková Barbora, Kimáková Patrícia, Ilkovičová Lenka, Szentpéteriová Erika, Debeljak Nataša, Solárová Zuzana, Sačková Veronika, Šemeláková Martina, Bhide Mangesh, Solár Peter
Department of Cell Biology, Institute of Biology and Ecology, Faculty of Science, Pavol Jozef Šafárik University in Košice, SK-04154 Košice, Slovak Republic.
Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Oncol Lett. 2016 Aug;12(2):1575-1580. doi: 10.3892/ol.2016.4782. Epub 2016 Jun 24.
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.
促红细胞生成素受体(EpoR)是细胞因子受体家族的成员。促红细胞生成素(Epo)与EpoR之间的相互作用对于红系细胞的产生和成熟很重要,从而刺激造血作用。在肿瘤细胞中也检测到EpoR这一事实引发了关于重组Epo治疗癌症患者贫血相关性的问题。大量研究报道了Epo在癌细胞中的促刺激和抗凋亡作用,从而证明了这些细胞中EpoR的功能。相比之下,先前的一项研究声称肿瘤细胞中不存在EpoR。据某些作者称,这种明显的差异是基于使用了非特异性抗EpoR抗体。为了绕过用抗EpoR抗体直接检测EpoR,本文作者提出了一种蛋白质印迹法,此外,该方法还证实了Epo与EpoR的相互作用。应用该技术,证实了人卵巢腺癌A2780细胞和正常人脐静脉内皮细胞中存在EpoR及其与Epo的相互作用。此外,对EpoR进行改良免疫沉淀,随后进行基质辅助激光解吸/电离飞行时间质谱分析,证实了一种57 kDa的蛋白质是这两种细胞系中与人Epo相互作用的蛋白质。