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Br J Cancer. 2008 Mar 25;98(6):1059-67. doi: 10.1038/sj.bjc.6604220. Epub 2008 Mar 18.

Erythropoietin receptor transcription is neither elevated nor predictive of surface expression in human tumour cells.

Author information

  • 1Amgen Inc., One Amgen Center Drive, Thousand Oaks, CA 91362, USA. anguss@amgen.com

Abstract

Erythropoietin receptor (EpoR) has been reported to be overexpressed in tumours and has raised safety concerns regarding the use of erythropoiesis-stimulating agents (ESAs) to treat anaemia in cancer patients. To investigate the potential for EpoR to be overexpressed in tumours, we have evaluated human tumours for amplification of the EPOR locus, levels of EPOR transcripts, and expression of surface EpoR protein. Gene amplification analysis of 1083 solid tumours found that amplification of the EPOR locus was rare with frequencies similar to other non-oncogenes. EPOR transcript levels in tumours and tumour cell lines were low in comparison with bone marrow and were equivalent to, or lower than, levels in normal tissues of tumour origin. Although EpoR mRNA was detected in some tumour lines, no EpoR could be detected on the cell surface using (125)I-Epo binding studies. This may be due to the lack of EpoR protein expression or lack of cell-surface-trafficking factors, such as Jak2. Taken together, we have found no evidence that EpoR is overexpressed in tumours or gets to the surface of tumour cells. This suggests that there is no selective advantage for tumours to overexpress EpoR and questions the functional relevance of EpoR gene transcription in tumours.

PMID:
18349818
[PubMed - indexed for MEDLINE]
PMCID:
PMC2275479
Free PMC Article

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