TY - JOUR
T1 - Novel antibodies directed against the human erythropoietin receptor: creating a basis for clinical implementation
AU - Maxwell, Perry
AU - Melendez-Rodriguez, Florinda
AU - Matchett, Kyle B.
AU - Julian, Aragones
AU - Ben-Califa, Nathalie
AU - Jaekel, Heidelinde
AU - Hengst, Ludger
AU - Lindner, Herbert
AU - Bernardini, Andre
AU - Brockmeier, Ulf
AU - Fandrey, Joachim
AU - Grunert, Fritz
AU - Oster, Howard, S.
AU - Mittelman, Moshe
AU - El-Tanani, Mohamed El-Tanani
AU - Thiersch, Markus
AU - Schneider Gasser, Edith M.
AU - Gassmann, Max
AU - Dangoor, David
AU - Cuthbert, Robert J.
AU - Irvine, Alexandra
AU - Jordan, Anne
AU - Lappin, Terence
AU - Thompson, John
AU - Neumann, Drorit
PY - 2015/2
Y1 - 2015/2
N2 - Recombinant human erythropoietin (rHuEPO) is an effective treatment for anaemia but concerns that it causes disease progression in cancer patients by activation of EPO receptors (EPOR) in tumour tissue have been controversial and have restricted its clinical use. Initial clinical studies were flawed because they used polyclonal antibodies, later shown to lack specificity for EPOR. Moreover, multiple isoforms of EPOR caused by differential splicing have been reported in cancer cell lines at the mRNA level but investigations of these variants and their potential impact on tumour progression, have been hampered by lack of suitable antibodies. The EpoCan consortium seeks to promote improved pathological testing of EPOR, leading to safer clinical use of rHuEPO, by producing well characterized EPOR antibodies.Using novel genetic and traditional peptide immunization protocols, we have produced mouse and rat monoclonal antibodies, and show that several of these specifically recognize EPOR by Western blot, immunoprecipitation, immunofluorescence, flow cytometry and immunohistochemistry in cell lines and clinical material. Widespread availability of these antibodies should enable the research community to gain a better understanding of the role of EPOR in cancer, and eventually to distinguish patients who can be treated safely by rHuEPO from those at increased risk from treatment.
AB - Recombinant human erythropoietin (rHuEPO) is an effective treatment for anaemia but concerns that it causes disease progression in cancer patients by activation of EPO receptors (EPOR) in tumour tissue have been controversial and have restricted its clinical use. Initial clinical studies were flawed because they used polyclonal antibodies, later shown to lack specificity for EPOR. Moreover, multiple isoforms of EPOR caused by differential splicing have been reported in cancer cell lines at the mRNA level but investigations of these variants and their potential impact on tumour progression, have been hampered by lack of suitable antibodies. The EpoCan consortium seeks to promote improved pathological testing of EPOR, leading to safer clinical use of rHuEPO, by producing well characterized EPOR antibodies.Using novel genetic and traditional peptide immunization protocols, we have produced mouse and rat monoclonal antibodies, and show that several of these specifically recognize EPOR by Western blot, immunoprecipitation, immunofluorescence, flow cytometry and immunohistochemistry in cell lines and clinical material. Widespread availability of these antibodies should enable the research community to gain a better understanding of the role of EPOR in cancer, and eventually to distinguish patients who can be treated safely by rHuEPO from those at increased risk from treatment.
U2 - 10.1111/bjh.13133
DO - 10.1111/bjh.13133
M3 - Article
SN - 0007-1048
VL - 168
SP - 429
EP - 442
JO - British Journal of Haematology
JF - British Journal of Haematology
ER -