Erythropoietin Supports the Survival of Prostate Cancer, But Not Growth and Bone Metastasis

被引:12
作者
Shiozawa, Yusuke [1 ]
McGee, Samantha [1 ]
Pienta, Michael J. [1 ,2 ,3 ]
McGregor, Natalie [2 ,3 ]
Jung, Younghun [1 ]
Yumoto, Kenji [1 ]
Wang, Jingcheng [1 ]
Berry, Janice E. [1 ]
Pienta, Kenneth J. [2 ,3 ]
Taichman, Russell S. [1 ]
机构
[1] Univ Michigan, Sch Dent, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
PROSTATE; CANCER; ERYTHROPOIETIN; TUMOR; GROWTH; METASTASIS; RECEPTOR EXPRESSION; STIMULATING AGENTS; TUMOR-GROWTH; ANGIOGENESIS; CELLS; PROLIFERATION; INVOLVEMENT; INHIBITOR; INDUCTION; LINEAGE;
D O I
10.1002/jcb.24592
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Erythropoietin (Epo) is used in clinical settings to enhance hematopoietic function and to improve the quality of life for patients undergoing chemotherapy by reducing fatigue and the need for transfusions. However, several meta-analyses have revealed that Epo treatments are associated with an increased risk of mortality in cancer patients. In this study, we examined the role of Epo in prostate cancer (PCa) progression, using in vitro cell culture systems and in vivo bone metastatic assays. We found that Epo did not stimulate the proliferation of PCa cell lines, but did protect PCa cells from apoptosis. In animal models of PCa metastasis, no evidence was found to support the hypothesis that Epo enhances metastasis. Together, these findings suggest that Epo may be useful for treating severe anemia in PCa patients without increasing metastatic risk. J. Cell. Biochem. 114: 2471-2478, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:2471 / 2478
页数:8
相关论文
共 42 条
[1]  
Acs G, 2001, CANCER RES, V61, P3561
[2]   Erythropoietin and erythropoietin receptor expression in human prostate cancer [J].
Arcasoy, MO ;
Amin, K ;
Vollmer, RT ;
Jiang, XH ;
Demark-Wahmefried, W ;
Haroon, ZA .
MODERN PATHOLOGY, 2005, 18 (03) :421-430
[3]   Expression of erythropoietin receptor splice variants in human cancer [J].
Arcasoy, MO ;
Jiang, XH ;
Haroon, ZA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (04) :999-1007
[4]   The non-haematopoietic biological effects of erythropoietin [J].
Arcasoy, Murat O. .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 141 (01) :14-31
[5]   Erythropoietin regulates endothelial progenitor cells [J].
Bahlmann, FH ;
de Groot, K ;
Spandau, JM ;
Landry, AL ;
Hertel, B ;
Duckett, T ;
Boehm, SM ;
Menne, J ;
Haller, H ;
Fliser, D .
BLOOD, 2004, 103 (03) :921-926
[6]   Erythropoietin mediates tissue protection through an erythropoietin and common β-subunit heteroreceptor [J].
Brines, M ;
Grasso, G ;
Fiordaliso, F ;
Sfacteria, A ;
Ghezzi, P ;
Fratelli, M ;
Latini, R ;
Xie, QW ;
Smart, J ;
Su-Rick, CJ ;
Pobre, E ;
Diaz, D ;
Gomez, D ;
Hand, C ;
Coleman, T ;
Cerami, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (41) :14907-14912
[7]   Osteoblastic cells regulate the haematopoietic stem cell niche [J].
Calvi, LM ;
Adams, GB ;
Weibrecht, KW ;
Weber, JM ;
Olson, DP ;
Knight, MC ;
Martin, RP ;
Schipani, E ;
Divieti, P ;
Bringhurst, FR ;
Milner, LA ;
Kronenberg, HM ;
Scadden, DT .
NATURE, 2003, 425 (6960) :841-846
[8]  
Dempke W, 2000, ANTICANCER RES, V20, P5155
[9]   Erythropoietin in cancer patients: pros and cons [J].
Dicato, Mario ;
Plawny, Laurent .
CURRENT OPINION IN ONCOLOGY, 2010, 22 (04) :307-311
[10]   Induction of signalling in non-erythroid cells by pharmacological levels of erythropoietin [J].
Dunlop, E. A. ;
Percy, M. J. ;
Boland, M. P. ;
Maxwell, A. P. ;
Lappin, T. R. .
NEURODEGENERATIVE DISEASES, 2006, 3 (1-2) :94-100