TY - JOUR
T1 - Preclinical studies of erythropoietin receptor expression in tumour cells: Impact on clinical use of erythropoietic proteins to correct cancer-related anaemia
AU - Österborg, Anders
AU - Aapro, Matti
AU - Cornes, Paul
AU - Haselbeck, Anton
AU - Hayward, Colin R.W.
AU - Jelkmann, Wolfgang
N1 - Funding Information:
This review was funded by F. Hoffmann-La Roche Ltd, Basel, Switzerland. Responsibility for opinions, conclusions, and interpretation of data lies with the authors.
Funding Information:
A.O. and M.A. have received research funding from Roche. M.A., P.C. and W.J. have served as consultants for and received honoraria from Amgen, Roche and Ortho Biotech. A.H. is employed by Roche Diagnostics GmbH and CRWH is employed by F. Hoffmann-La Roche.
Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2007/2
Y1 - 2007/2
N2 - In vitro and animal model studies have shown erythropoietin receptor (Epo-R) mRNA and/or protein may be present in a range of human tumours and cancer cell lines, and erythropoiesis-stimulating agents (ESAs) have been reported to have tumour cell growth-modulating effects. Following a review of the literature, we conclude that considerations must be made when interpreting data from the preclinical studies. First, supraphysiological doses of ESAs were usually used. Second, there are no well validated, commercially available antibodies for identifying the presence and functionality of Epo-R at the protein level, either intracellularly or on the cell surface. Data from previous studies that used antibodies only for Epo-R detection must therefore be interpreted with caution. Together with diverging results in the literature, these methodological limitations indicate that findings from preclinical studies must not be over-translated in terms of their clinical relevance to patients with cancer.
AB - In vitro and animal model studies have shown erythropoietin receptor (Epo-R) mRNA and/or protein may be present in a range of human tumours and cancer cell lines, and erythropoiesis-stimulating agents (ESAs) have been reported to have tumour cell growth-modulating effects. Following a review of the literature, we conclude that considerations must be made when interpreting data from the preclinical studies. First, supraphysiological doses of ESAs were usually used. Second, there are no well validated, commercially available antibodies for identifying the presence and functionality of Epo-R at the protein level, either intracellularly or on the cell surface. Data from previous studies that used antibodies only for Epo-R detection must therefore be interpreted with caution. Together with diverging results in the literature, these methodological limitations indicate that findings from preclinical studies must not be over-translated in terms of their clinical relevance to patients with cancer.
UR - http://www.scopus.com/inward/record.url?scp=33846615414&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2006.10.012
DO - 10.1016/j.ejca.2006.10.012
M3 - Journal articles
C2 - 17150352
AN - SCOPUS:33846615414
SN - 0959-8049
VL - 43
SP - 510
EP - 519
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 3
ER -