Erythropoietin improves cardiac wasting and outcomes in a rat model of liver cancer cachexia.
暂无分享,去创建一个
S. Anker | S. von Haehling | Masakazu Saitoh | Junichi Ishida | N. Ebner | J. Springer | S. Palus | M. Konishi | Michiyoshi Hatanaka | W. Döhner
[1] F. López‐Soriano,et al. Nonmuscle Tissues Contribution to Cancer Cachexia , 2015, Mediators of inflammation.
[2] S. Anker,et al. Cardiovascular function and predictors of exercise capacity in patients with colorectal cancer. , 2014, Journal of the American College of Cardiology.
[3] S. Anker,et al. Prevention of liver cancer cachexia-induced cardiac wasting and heart failure. , 2014, European heart journal.
[4] V. Baracos,et al. Concurrent evolution of cancer cachexia and heart failure: bilateral effects exist , 2014, Journal of cachexia, sarcopenia and muscle.
[5] F. López‐Soriano,et al. Erythropoietin administration partially prevents adipose tissue loss in experimental cancer cachexia models , 2013, Journal of Lipid Research.
[6] W. Evans,et al. Longitudinal changes in total body creatine pool size and skeletal muscle mass using the D3-creatine dilution method , 2013, Journal of cachexia, sarcopenia and muscle.
[7] S. Anker,et al. Ursodeoxycholic acid treatment in a rat model of cancer cachexia , 2011, Journal of cachexia, sarcopenia and muscle.
[8] E. Barrey,et al. Skeletal muscle alterations and exercise performance decrease in erythropoietin-deficient mice: a comparative study , 2012, BMC Medical Genomics.
[9] F. López‐Soriano,et al. Formoterol and cancer muscle wasting in rats: Effects on muscle force and total physical activity. , 2011, Experimental and therapeutic medicine.
[10] D. Lacey,et al. Reversal of Cancer Cachexia and Muscle Wasting by ActRIIB Antagonism Leads to Prolonged Survival , 2010, Cell.
[11] F. Berger,et al. Activity level, apoptosis, and development of cachexia in Apc(Min/+) mice. , 2010, Journal of applied physiology.
[12] S. Anker,et al. No effects of human ghrelin on cardiac function despite profound effects on body composition in a rat model of heart failure. , 2009, International journal of cardiology.
[13] M. Aapro,et al. Update on erythropoiesis-stimulating agents and clinical trials in oncology. , 2009, The oncologist.
[14] A. Cerami,et al. Erythropoietin‐mediated tissue protection: reducing collateral damage from the primary injury response , 2008, Journal of internal medicine.
[15] G. Takemura,et al. Reduction of inflammatory cytokine expression and oxidative damage by erythropoietin in chronic heart failure. , 2006, Cardiovascular research.
[16] Kenta Ito,et al. Endogenous erythropoietin system in non-hematopoietic lineage cells plays a protective role in myocardial ischemia/reperfusion. , 2006, Cardiovascular research.
[17] A. Cerami,et al. Discovering erythropoietin's extra-hematopoietic functions: biology and clinical promise. , 2006, Kidney international.
[18] L. Annemans,et al. European guidelines for the management of chemotherapy-induced anaemia and health economic aspects of treatment. , 2006, Cancer treatment reviews.
[19] M. Kawakami,et al. Erythropoietin attenuates cachectic events and decreases production of interleukin-6, a cachexia-inducing cytokine. , 2005, Cytokine.
[20] E. Lakatta,et al. Cardioprotection by Recombinant Human Erythropoietin Following Acute Experimental Myocardial Infarction: Dose Response and Therapeutic Window , 2005, Cardiovascular Drugs and Therapy.
[21] J. Barton,et al. Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population , 2004, BMC Medical Genetics.
[22] P. Ghezzi,et al. Erythropoietin mediates tissue protection through an erythropoietin and common beta-subunit heteroreceptor. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[23] Dirk Schrijvers,et al. The European Cancer Anaemia Survey (ECAS): a large, multinational, prospective survey defining the prevalence, incidence, and treatment of anaemia in cancer patients. , 2004, European journal of cancer.
[24] S. E. Samuels,et al. The role of ubiquitin-proteasome-dependent proteolysis in the remodelling of skeletal muscle. , 2004, The Proceedings of the Nutrition Society.
[25] A. Cerami,et al. Erythropoietin as a Tissue-Protective Cytokine in Brain Injury: What Do We Know and Where Do We Go? , 2004, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[26] L. Harrison,et al. Once‐weekly dosing of epoetin‐α increases hemoglobin and improves quality of life in anemic cancer patients receiving radiation therapy either concomitantly or sequentially with chemotherapy , 2003, Cancer.
[27] S. Anker,et al. Cytokines, apoptosis and cachexia: the potential for TNF antagonism. , 2002, International journal of cardiology.
[28] J. Madelmont,et al. Chemotherapy inhibits skeletal muscle ubiquitin-proteasome-dependent proteolysis. , 2002, Cancer research.
[29] M. McKenzie,et al. Epoetin alfa therapy increases hemoglobin levels and improves quality of life in patients with cancer-related anemia who are not receiving chemotherapy and patients with anemia who are receiving chemotherapy. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[30] P. Barrett-Lee,et al. Improvement in quality of life for cancer patients treated with epoetin alfa. , 2001, European journal of cancer care.
[31] A. Billiau,et al. Cytokines and cachexia. , 1997, Nutrition.
[32] L. Tessitore,et al. Tumor necrosis factor-alpha mediates changes in tissue protein turnover in a rat cancer cachexia model. , 1993, The Journal of clinical investigation.
[33] E. Aulbert. [Anemia in malignant tumor diseases. II. Tumor-induced loss of transferrin as a cause of the development of anemia based on a rat model]. , 1989, Nuklearmedizin. Nuclear medicine.